Search results

  1. WIBRe001-A-43 (WIBR3_GBA1_IVS2_Het_10C2F)

    United States Albert Einstein College of Medicine (AECM)
    Disease:

    Parkinson disease

  2. WIBRe001-A-44 (WIBR3_GBA1_IVS2_Het_10D11A)

    United States Albert Einstein College of Medicine (AECM)
    Disease:

    Parkinson disease

  3. WIBRe001-A-49 (WIBR3_ATP13A2_FS_Homo_12_6)

    United States Albert Einstein College of Medicine (AECM)
    Disease:

    Parkinson disease

  4. WIBRe001-A-50 (WIBR3_ATP13A2_FS_Homo_12_2)

    United States Albert Einstein College of Medicine (AECM)
    Disease:

    Parkinson disease

  5. WIBRe001-A-51 (WIBR3_ATP13A2_FS_Homo_ 6_1)

    United States Albert Einstein College of Medicine (AECM)
    Disease:

    Parkinson disease

  6. WIBRe001-A-52 (WIBR3_ATP13A2_FS_ 5_6)

    United States Albert Einstein College of Medicine (AECM)
    Disease:

    Parkinson disease

  7. WIBRe001-A-53 (WIBR3_ATP13A2_FS_Homo_2_5)

    United States Albert Einstein College of Medicine (AECM)
    Disease:

    Parkinson disease

  8. WIBRe001-A-54 (WIBR3_VPS13C_FS_Homo_E10-2)

    United States Albert Einstein College of Medicine (AECM)
    Disease:

    Parkinson disease

  9. WIBRe001-A-58 (WIBR3_VPS13C_FS_Homo_H3-1)

    United States Albert Einstein College of Medicine (AECM)
    Disease:

    Parkinson disease

  10. WAe009-A-36 (JPH2-KO)

    China Anzhen Hospital (ANZHEN)
    Disease:

    Hypertrophic cardiomyopathy

  11. ASGRCi002-A (F3-3#1 CHR)

    Taiwan Genomics Research Center (ASGRC)
    Disease:

    Type 1 diabetes mellitus

  12. ASGRCi003-A (F3-4#5 CHR)

    Taiwan Genomics Research Center (ASGRC)
    Disease:

    Type 1 diabetes mellitus

  13. ATLABi008-A (AT-UC I Normal-iC06)

    Singapore IMCB, Adrian Teo's Lab (ATLAB)
    Disease:

    Normal (average)

  14. ATLABi009-A (AT-UC I Normal-iC13)

    Singapore IMCB, Adrian Teo's Lab (ATLAB)
    Disease:

    Normal (average)

  15. BBANTWi012-A-1 (TTN_E48_V4623*)

    Belgium Biobank Antwerpen (BBANTW)
    Disease:

    Dilated cardiomyopathy

  16. BBANTWi012-A-2 (iPSC_FB_F19901C3_TTN_E48_L4612*)

    Belgium Biobank Antwerpen (BBANTW)
    Disease:

    Dilated cardiomyopathy

  17. BCHi007-A (HNDS0005-01 #B)

    United States Children's Hospital (BCH)
    Disease:

    Succinic semialdehyde dehydrogenase deficiency

  18. BCHi009-A (HNDS0002-01 #D)

    United States Children's Hospital (BCH)
    Disease:

    Succinic semialdehyde dehydrogenase deficiency

  19. BCHi009-A-1 (HNDS0002-01 #D CC26 +/+)

    United States Children's Hospital (BCH)
    Disease:

    Succinic semialdehyde dehydrogenase deficiency

  20. BCHi011-A (HNDS0003-01 #F)

    United States Children's Hospital (BCH)
    Disease:

    Succinic semialdehyde dehydrogenase deficiency

  21. BCHi011-A-1 (HNDS0003-01 #F CC39 +/+)

    United States Children's Hospital (BCH)
    Disease:

    Succinic semialdehyde dehydrogenase deficiency

  22. BCHi030-B (HNDS0131-01#I)

    United States Children's Hospital (BCH)
    Disease:

    Tuberous sclerosis complex

  23. BCHi047-A (HNDS0056-02#A)

    United States Children's Hospital (BCH)
    Disease:

    Phelan-mcdermid syndrome

  24. BCMi001-B (M22c8 and HSCC-003iPS-Sc8)

    United States Baylor College of Medicine (BCM)
    Disease:

    Normal (average)

  25. BCRTi002-A (P02-1)

    Germany Berlin-Brandenburg Center for Regenerative Therapies (BCRT)
    Disease:

    Fibrodysplasia ossificans progressiva

  26. BCRTi007-A

    Germany Berlin-Brandenburg Center for Regenerative Therapies (BCRT)
    Disease:

    Polycystic kidney disease

  27. BIHi001-A-1 (iBCRT Cas9v1-3G-Kl.16)

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal (average)

  28. SIGi001-A-14 (SIGi001-A Bi-Allelic MAPT HA-tag)

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

  29. SIGi001-A-16 (SIGi001-A-9 Bi-Allelic MAPT HA-tag)

    Denmark Bioneer (BION)
    Disease:

    Frontotemporal dementia

  30. STBCi006-A-1 (ApoE KO)

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

  31. BIONi010-C-71 (BIONi010-C with an APOE 3/3 genotype with an additional, homozygous christchurch mutation)

    Denmark Bioneer (BION)
    Disease:

    Alzheimer's disease

  32. BIORTCi001-A (BAiPSC 000 and OSTiFGM2)

    Nigeria Biomedical Science Research and Training Centre (BIORTC)
    Disease:

    Normal (average)

  33. BUCREMi001-A (iPSC-S6D63H-1-hom)

    United States Boston University (BUCREM)
    Disease:

    Lethal brain and heart developmental defects

  34. WIBRe001-A-4 (WIBR3_PRKN_X3DEL_B1-3)

    United States University of California, Berkeley (CAL)
    Disease:

    Parkinson disease

  35. WIBRe001-A-5 (WIBR3_PRKN_X3DEL_F2-5)

    United States University of California, Berkeley (CAL)
    Disease:

    Parkinson disease

  36. WIBRe001-A-6 (WIBR3_PRKN_X3DEL_H2-2)

    United States University of California, Berkeley (CAL)
    Disease:

    Parkinson disease

  37. WIBRe001-A-10 (WIBR3_FBXO7_FS_A3-1)

    United States University of California, Berkeley (CAL)
    Disease:

    Parkinson disease

  38. WIBRe001-A-15 (WIBR3_DNAJC6_c.801-2 A>G+FS/c.801-2 A>G_G12-2)

    United States University of California, Berkeley (CAL)
    Disease:

    Parkinson disease

  39. WIBRe001-A-16 (WIBR3_DNAJC6_FS/FS_H10-1)

    United States University of California, Berkeley (CAL)
    Disease:

    Parkinson disease

  40. CAMi014-A (A1ATD1)

    United Kingdom University of Cambridge (CAM)
    Disease:

    Alpha-1-antitrypsin deficiency

  41. CBDTi001-A

    India Institute for Stem Cell Science and Regenerative Medicine (CBDT)
    Disease:

    Normal (average)

  42. CBIGi001-A (AIW002-02)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Normal (average)

  43. CCMi001-A (DMD1)

    Italy Centro Cardiologico Monzino IRCCS (CCM)
    Disease:

    Duchenne muscular dystrophy

  44. CHCMUi002-A

    China Children's hospital of Chongqing Medical University (CHCMU)
    Disease:

    Chronic granulomatous disease

  45. CHOCi005-A

    United States CHOC Children's (CHOC)
    Disease:

    Gm1 gangliosidosis

  46. WAe001-A-2I (H1 INS-PPImNG and CHOPe004-A-2I)

    United States The Children's Hospital of Philadelphia (CHOP)
    Disease:

    Normal (average)

  47. CHUVi001-A

    Switzerland Centre Hospitalier Universitaire Vaudois (CHUV)
    Disease:

    Normal (average)

  48. CIGLi001-A (RPChiPS8023G1, iPSC TBX4 WT, StemRNA™ Human iPSC 802-3G and SYNTHEGO 802-30F)

    United States Center for Infection and Genomics of the Lung (CIGL)
    Disease:

    Normal (average)

  49. CIRMi285-A (CW70022)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Diabetic retinopathy

  50. CIRMi286-A (CW70028)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 1 diabetes mellitus

  51. CIRMi287-A (CW70029)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 1 diabetes mellitus

  52. CIRMi292-A (CW70035)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Diabetic retinopathy

  53. CIRMi293-A (CW70036)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Diabetic retinopathy

  54. CIRMi294-A (CW70037)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 1 diabetes mellitus

  55. CIRMi307-A (CW70052)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 1 diabetes mellitus

  56. CIRMi314-A (CW70064)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Diabetic retinopathy

  57. CIRMi323-A (CW70085)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Diabetic retinopathy

  58. CIRMi329-A (CW70091)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Diabetic retinopathy

  59. CIRMi361-A (CW70129)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Diabetic retinopathy

  60. CIRMi373-A (CW70143)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 1 diabetes mellitus

  61. CIRMi419-A (CW70208)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 1 diabetes mellitus

  62. CIRMi451-A (CW70254)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 1 diabetes mellitus

  63. CIRMi484-A (CW70296)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Diabetic retinopathy

  64. CIRMi498-A (CW70313)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Diabetic retinopathy

  65. CIRMi499-A (CW70314)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 1 diabetes mellitus

  66. CIRMi505-A (CW70320)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 1 diabetes mellitus

  67. CIRMi511-A (CW70326)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Diabetic retinopathy

  68. CIRMi526-A (CW70350)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 1 diabetes mellitus

  69. CIRMi528-A (CW70353)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 1 diabetes mellitus

  70. CIRMi538-A (CW70369)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 1 diabetes mellitus

  71. CIRMi03Z-A (CW30461)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  72. CMGANTi003-A (SEMD1)

    Belgium Center of Medical Genetics Antwerp (CMGANT)
    Disease:

    X-linked spondyloepimetaphyseal dysplasia

  73. CMGANTi004-A (SEMD2)

    Belgium Center of Medical Genetics Antwerp (CMGANT)
    Disease:

    X-linked spondyloepimetaphyseal dysplasia

  74. CMGANTi006-A (SEDC1)

    Belgium Center of Medical Genetics Antwerp (CMGANT)
    Disease:

    Spondyloepiphyseal dysplasia congenita

  75. CMGANTi007-A (SEDC2)

    Belgium Center of Medical Genetics Antwerp (CMGANT)
    Disease:

    Spondyloepiphyseal dysplasia congenita

  76. CMGANTi008-A (iPSC_MFS_FBN1_Fi930129_C8)

    Belgium Center of Medical Genetics Antwerp (CMGANT)
    Disease:

    Marfan syndrome

  77. CRICKi003-A (iFCI002)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Intellectual disability

  78. CRICKi004-A (iFCI008)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Spinal muscular atrophy with lower extremity predominant

  79. CRICKi005-A (iFCI004)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Spinal muscular atrophy

  80. CRICKi006-A (iFCI005)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Spinal muscular atrophy

  81. CRICKi007-A (iFCI009)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Spinal muscular atrophy with lower extremity predominant

  82. CRICKi008-A (iFCI006 and NH13-0078)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    X-linked centronuclear myopathy

  83. CRICKi009-A (iFCI012 and iFCI012 CLONE 4)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Vhl

  84. CRICKi010-A (iFCI013 and iFCI013 Clone 7)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Vhl

  85. CRICKi011-A (iFCI016)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Young-onset parkinson disease

  86. CRICKi012-A (iFCI017)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Young-onset parkinson disease

  87. CRICKi013-A (iFCI018 Clone 6)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Von hippel-lindau disease tumor suppressor

  88. CRICKi014-A (iFCI019 Clone 4)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Von hippel-lindau disease tumor suppressor

  89. CRICKi015-A (iFCI020 Clone 1)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Von hippel-lindau disease tumor suppressor

  90. CRICKi016-A (iFCI021 Clone 7)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Lung cancer

  91. CRICKi017-A (iFCI022 Clone 4)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Lung cancer

  92. CRICKi018-A (iKER 12 and iFCI023)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Normal (average)

  93. CRICKi019-A (iKER 8 and iFCI024)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Normal (average)

  94. CRICKi020-A (iFCI025 and iKER 10)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Normal (average)

  95. CRICKi021-A (iFCI007)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Ullrich congenital muscular dystrophy

  96. CRICKi022-A (iFCI031)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Lung cancer

  97. CRICKi023-A (iFCI032)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Lung squamous cell carcinoma

  98. CRTDi001-A (T12.9 and C1-1)

    Germany Center for Regenerative Therapies Dresden (CRTD)
    Disease:

    Normal (average)

  99. CSCIi001-A (niPSC HDF16 and niPSC-16.2b)

    United Kingdom Wellcome Trust - MRC Stem Cell Institute (CSCI)
    Disease:

    Normal (average)

  100. CSCIi002-A (niPSC HDF75 and niPSC-75.1c2)

    United Kingdom Wellcome Trust - MRC Stem Cell Institute (CSCI)
    Disease:

    Normal (average)

  101. CSSi001-A (Joub03cl2 and COR419)

    Italy Fondazione Casa Sollievo della Sofferenza IRCCS (CSS)
    Disease:

    Joubert syndrome

  102. CSSi015-A (FC17)

    Italy Fondazione Casa Sollievo della Sofferenza IRCCS (CSS)
    Disease:

    Normal (average)

  103. CSUXHi003-A

    China Xiangya Hospital (CSUXH)
    Disease:

    Waardenburg syndrome type 2

  104. CSUXHi004-A

    China Xiangya Hospital (CSUXH)
    Disease:

    Waardenburg syndrome type 1

  105. CTEFi001-A (CTEF-hiPSC10 and FNUSA-hiPSC10)

    Czech Republic Cell and Tissue Engineering Facility (CTEF)
    Disease:

    Normal (average)

  106. DMBi001-A-2

    Poland Department of Medical Biotechnology (DMB)
    Disease:

    Normal (average)

  107. WAe009-A-58 (COL4A5 heterozygote)

    China Dongzhimen Hospital Affiliated to Beijing University of Chinese Medicine (DZMH)
    Disease:

    Alport syndrome

  108. EDi010-A (RCi136)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Bipolar disorder

  109. EDi010-B (RCi138)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Bipolar disorder

  110. EDi011-A (RCi139)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Bipolar disorder

  111. EDi011-B (RCi140)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Bipolar disorder

  112. EDi011-C (RCi141)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Bipolar disorder

  113. EDi018-B (RCi212)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Bipolar disorder

  114. EDi018-C (RCi213)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Bipolar disorder

  115. EDi046-A

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal (average)

  116. EHTJUi002-A (DF-GMP-ZB11AR-H)

    China East Hospital Affiliated to Tongji University (EHTJU)
    Disease:

    Normal (average)

  117. EHTJUi004-A (DF-GMP-ZB12AN-I)

    China East Hospital Affiliated to Tongji University (EHTJU)
    Disease:

    Normal (average)

  118. ESi065-A ([IDDM1] FiPS 1.13-Ep6F-9)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Obsolete_type i diabetes mellitus

  119. ESi080-A (N1-FiPS4F#7)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  120. ESi104-A (PMM2-CDG FiPS48-Sv4F-7)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Pmm2-cdg

  121. ESi112-A

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  122. FDCHDPi001-A (FDCHDP01)

    China Fudan University (FDCHDP)
    Disease:

    Tourette syndrome

  123. FMMUNIi001-A (I-WT)

    Czech Republic Faculty of Medicine, Masaryk University (FMMUNI)
    Disease:

    Normal (average)

  124. FMMUNIi002-A (I-IF)

    Czech Republic Faculty of Medicine, Masaryk University (FMMUNI)
    Disease:

    Ventricular fibrillation

  125. FMMUNIi003-A (I-CPVT)

    Czech Republic Faculty of Medicine, Masaryk University (FMMUNI)
    Disease:

    Catecholaminergic polymorphic ventricular tachycardia

  126. GENEAe008-A (GENEA009 and SIVF09)

    Australia Genea (GENEA)
  127. GENEAe013-A (GENEA089)

    Australia Genea (GENEA)
    Disease:

    Huntington disease

  128. GENEAe014-A (GENEA029)

    United States Genea (GENEA)
    Disease:

    Normal (average)

  129. GENEAe015-A (GENEA020)

    United States Genea (GENEA)
    Disease:

    Huntington disease

  130. GENEAe017-A (GENEA023)

    Australia Genea (GENEA)
    Disease:

    Normal (average)

  131. GENEAe018-A (GENEA090)

    Australia Genea (GENEA)
    Disease:

    Huntington disease

  132. GENEAe019-A (GENEA091)

    Australia Genea (GENEA)
    Disease:

    Huntington disease

  133. GENYOi001-A (PBMC1-iPS4F1)

    Spain Centre for Genomics and Oncological Research (GENYO)
    Disease:

    Normal (average)

  134. GENYOi003-A (PBMC2-iPS4F8)

    Spain Centre for Genomics and Oncological Research (GENYO)
    Disease:

    Normal (average)

  135. GENYOi004-A (ASD-PBMC-iPS4F2)

    Spain Centre for Genomics and Oncological Research (GENYO)
    Disease:

    Adnp syndrome

  136. GENYOi005-A (FPD/AML-PBMC-iPSC4F73)

    Spain Centre for Genomics and Oncological Research (GENYO)
    Disease:

    Familial platelet disorder with associated myeloid malignancy

  137. WAe009-A-84

    China Guangxi Institute of Cardiovascular Diseases (GICD)
    Disease:

    Congenital heart disease

  138. WAe001-A-2C (SST-P2A-mCherry)

    China Guangzhou Laboratory (GL)
    Disease:

    Normal (average)

  139. GRCHJUi001-A (LYJ-iPS-C)

    China Guangzhou Red Cross Hospital of Jinan University (GRCHJU)
    Disease:

    Atrial fibrillation

  140. HCORDi001-I (M2_IPSC4_P)

    Brazil Hemocord Clínica Médica Ltda (HCORD)
    Disease:

    Normal (average)

  141. HEBHMUi010-A

    China Hebei Medical University (HEBHMU)
    Disease:

    Normal (average)

  142. HELPi001-A (BS-TL-1)

    China Help Stem Cell Innovations Co.Ltd. (HELP)
    Disease:

    Congenital contractural arachnodactyly

  143. HHUi003-B (A4_C1)

    Germany Universitätsklinikum Düsseldorf (HHU)
    Disease:

    Maternally-inherited leigh syndrome

  144. HHUi003-C (A4_W1)

    Germany Universitätsklinikum Düsseldorf (HHU)
    Disease:

    Maternally-inherited leigh syndrome

  145. HHUi006-A (11656_H)

    Germany Universitätsklinikum Düsseldorf (HHU)
    Disease:

    Normal (average)

  146. HHUi006-B (11656_K)

    Germany Universitätsklinikum Düsseldorf (HHU)
    Disease:

    Normal (average)

  147. HNMUi009-A (iPS-UC1171)

    China Hainan Medical University (HNMU)
    Disease:

    Thalassemia

  148. HVRDi005-A (BJ SiPS-D)

    United States Harvard University (HVRD)
    Disease:

    Normal (average)

  149. IBBISTi010-A (4_H17)

    Portugal Simão José Teixeira da Rocha (IBBIST)
    Disease:

    Hypertrophic cardiomyopathy

  150. IBBISTi011-A (3_H24)

    Portugal Simão José Teixeira da Rocha (IBBIST)
    Disease:

    Hypertrophic cardiomyopathy

  151. IBBISTi012-A (6_H35)

    Portugal Simão José Teixeira da Rocha (IBBIST)
    Disease:

    Hypertrophic cardiomyopathy

  152. IBBISTi013-A (4_H22)

    Portugal Simão José Teixeira da Rocha (IBBIST)
    Disease:

    Hypertrophic cardiomyopathy

  153. IBKMOLi003-A (vEDS COL3A1 Q105* iPSC)

    Austria University of Innsbruck, Institute of Molecular Biology (IBKMOL)
    Disease:

    Vascular ehlers-danlos syndrome

  154. IBKMOLi004-A (sCeAD iPSC)

    Austria University of Innsbruck, Institute of Molecular Biology (IBKMOL)
  155. IBKMOLi005-A (CTRL iPSC)

    Austria University of Innsbruck, Institute of Molecular Biology (IBKMOL)
    Disease:

    Normal (average)

  156. IBPi002-A (P71 iPSCs 1)

    Czech Republic Institute of Biophysics of the Czech Academy of Sciences (IBP)
    Disease:

    Prostate adenocarcinoma

  157. ICANi001-A (CDGEN1.16)

    France INSERM U1166-Institute of Cardiometabolism And Nutrition (ICAN)
    Disease:

    Hypertrophic cardiomyopathy

  158. ICANi001-A-1 (CDGEN1.16.40.5)

    France INSERM U1166-Institute of Cardiometabolism And Nutrition (ICAN)
    Disease:

    Hypertrophic cardiomyopathy

  159. ICANi002-A (ICAN-403.3)

    France INSERM U1166-Institute of Cardiometabolism And Nutrition (ICAN)
    Disease:

    Normal (average)

  160. ICANi002-A-1 (ICAN-FLNC42.1)

    France INSERM U1166-Institute of Cardiometabolism And Nutrition (ICAN)
    Disease:

    Normal (average)

  161. ICANi002-A-3 (ICAN-BAG3-V468MC34)

    France INSERM U1166-Institute of Cardiometabolism And Nutrition (ICAN)
    Disease:

    Dilated cardiomyopathy 1hh

  162. ICANi002-A-4 (ICAN_BAG3_M468MC19)

    France INSERM U1166-Institute of Cardiometabolism And Nutrition (ICAN)
    Disease:

    Dilated cardiomyopathy 1hh

  163. ICANi002-A-5 (ICAN-PKP2-H695-W11)

    France INSERM U1166-Institute of Cardiometabolism And Nutrition (ICAN)
    Disease:

    Arrhythmogenic right ventricular dysplasia 9

  164. ICGi002-A (DMD1_1)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Duchenne muscular dystrophy

  165. ICGi002-B (DMD1_4)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Duchenne muscular dystrophy

  166. ICGi002-C (DMD1_11)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Duchenne muscular dystrophy

  167. ICGi003-A (f3SMA3)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Spinal muscular atrophy type 3

  168. ICGi005-A (iSMA40)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Proximal spinal muscular atrophy type 1

  169. ICGi005-B (iSMA37)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Proximal spinal muscular atrophy type 1

  170. ICGi006-A (m3SMA13)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Proximal spinal muscular atrophy type 2

  171. ICGi006-B (m3SMA20)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Proximal spinal muscular atrophy type 2

  172. ICGi007-A (47Q-3Lf)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Huntington disease

  173. ICGi009-A (iTAF3-17 and iTAF3del17)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Intellectual disability

  174. ICGi009-B (iTAF3del37 and iTAF3-37)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Intellectual disability

  175. ICGi013-A (iTAF13-26 and iTAF13del26)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Intellectual disability

  176. ICGi013-B (iTAF13del27 and iTAF13-27)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Intellectual disability

  177. ICGi015-B-1 (m6.7pCyto-17)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Parkinson disease

  178. ICGi018-A (iHD38Q-3)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Huntington's disease

  179. ICGi018-B (iHD38Q-2)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Huntington's disease

  180. ICGi018-C (iHD38Q-1)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Huntington's disease

  181. ICGi019-A (HCM1f6)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Hypertrophic cardiomyopathy

  182. ICGi019-B (HCM1f33)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Hypertrophic cardiomyopathy

  183. ICGi021-A (K6-4f)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Normal (average)

  184. ICGi021-A-1 (K6-4fpCyto-13)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Healthy

  185. ICGi022-A (K7-4Lf)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Healthy subject

  186. ICGi025-A (iTAF11-4)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Developmental delay

  187. ICGi028-A (HCM4fm5.2)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Hypertrophic cardiomyopathy

  188. ICGi029-A (HCM14fm6.2)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Hypertrophic cardiomyopathy

  189. ICGi030-A (HF2)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Wilson disease

  190. IDVi006-A (UBAP1L-3225)

    France INSTITUT DE LA VISION (IDV)
    Disease:

    Retinal dystrophy

  191. IGIBi002-A

    India CSIR-Institute of Genomics and Integrative Biology (IGIB)
    Disease:

    Beta-thalassemia

  192. IGIBi019-A (iPSC V2b)

    India CSIR-Institute of Genomics and Integrative Biology (IGIB)
    Disease:

    Normal (average)

  193. IGIBi020-A (iPSC V1b)

    India CSIR-Institute of Genomics and Integrative Biology (IGIB)
    Disease:

    Normal (average)

  194. IGIBi021-A (iPSC V3b)

    India CSIR-Institute of Genomics and Integrative Biology (IGIB)
    Disease:

    Normal (average)

  195. IGIBi022-A (iPSC V2c)

    India CSIR-Institute of Genomics and Integrative Biology (IGIB)
    Disease:

    Normal (average)

  196. IGIBi023-A (iPSC V1c)

    India CSIR-Institute of Genomics and Integrative Biology (IGIB)
    Disease:

    Normal (average)

  197. IGIBi024-A (iPSC V3c)

    India CSIR-Institute of Genomics and Integrative Biology (IGIB)
    Disease:

    Normal (average)

  198. IGIBi025-A (iPSC V3a)

    India CSIR-Institute of Genomics and Integrative Biology (IGIB)
    Disease:

    Normal (average)

  199. IMBPASi001-A (iPSC-WFS1-#1)

    Poland Institute of Medical Biology of Polish Academy of Sciences (IMBPAS)
    Disease:

    Wolfram syndrome 1

  200. IMGTi001-A (iTAF5-29)

    Russia Research Institute of Medical Genetics, TNMRC (IMGT)
    Disease:

    Phelan-mcdermid syndrome

  201. INEUi004-A (FHL1-V)

    Argentina Instituto de Neurociencias Conicet (INEU)
    Disease:

    Muscular dystrophy

  202. INSAi003-A

    Portugal Instituto Nacional de Saude Ricardo Jorge (INSA)
    Disease:

    Mucolipidosis type ii

  203. INSRMi002-A (PC117_c2)

    France INSERM (INSRM)
    Disease:

    Epilepsy

  204. INSRMi003-A (PC128_c5)

    France INSERM (INSRM)
    Disease:

    Normal (average)

  205. INSRMi004-A (PC118_c7)

    France INSERM (INSRM)
    Disease:

    Epilepsy

  206. INSRMi005-A (PC119_c7)

    France INSERM (INSRM)
    Disease:

    Normal (average)

  207. INSRMi006-A (PC131_c8)

    France INSERM (INSRM)
    Disease:

    Epilepsy

  208. INSRMi007-A (pc132-c4)

    France INSERM (INSRM)
    Disease:

    Normal (average)

  209. INSRMe002-A (STR-I-233-FRAXA)

    France INSERM (INSRM)
    Disease:

    Fragile x syndrome

  210. INSRMe003-A (STR-I-155-HD)

    France INSERM (INSRM)
    Disease:

    Huntington disease

  211. INSRMe004-A (STR-I-171-GLA)

    France INSERM (INSRM)
    Disease:

    Fabry disease

  212. INSRMe005-A (STR-I-189-FRAXA)

    France INSERM (INSRM)
    Disease:

    Fragile x syndrome

  213. INSRMe006-A (STR-I-209-MEN2a)

    France INSERM (INSRM)
    Disease:

    Endocrine gland cancer

  214. INSRMe007-A (STR-I-211-MEN2a)

    France INSERM (INSRM)
    Disease:

    Endocrine gland cancer

  215. INSRMe008-A (STR-I-203-CFTR)

    France INSERM (INSRM)
    Disease:

    Cystic fibrosis

  216. INSRMe009-A (STR-I-251-CFTR)

    France INSERM (INSRM)
    Disease:

    Cystic fibrosis

  217. INSRMe010-A (STR-I-221-Sca2)

    France INSERM (INSRM)
    Disease:

    Autosomal dominant cerebellar ataxia

  218. INSRMe011-A (STR-I-229-MTMX)

    France INSERM (INSRM)
    Disease:

    X-linked myopathy with excessive autophagy

  219. INSRMe012-A (STR-I-231-MTMX)

    France INSERM (INSRM)
    Disease:

    X-linked myopathy with excessive autophagy

  220. INSRMe013-A (STR-I-301-MFS)

    France INSERM (INSRM)
    Disease:

    Marfan syndrome

  221. INSRMe014-A (STR-I-305-APC)

    France INSERM (INSRM)
    Disease:

    Familial adenomatous polyposis

  222. INSRMe015-A (STR-I-315-CMT1a)

    France INSERM (INSRM)
    Disease:

    Charcot-marie-tooth disease type 1

  223. INSRMe016-A (STR-I-347-FRAXA)

    France INSERM (INSRM)
    Disease:

    Fragile x syndrome

  224. INSRMe017-A (STR-I-355-APC)

    France INSERM (INSRM)
    Disease:

    Familial adenomatous polyposis

  225. INSRMe018-A (STR-I-359-APC)

    France INSERM (INSRM)
    Disease:

    Familial adenomatous polyposis

  226. ITXi013-A (PT-R406W)

    France l’institut du thorax (ITX)
    Disease:

    Desminopathy

  227. JNCHi002-A (JNCHi002-A)

    China Jinan children's Hospital (JNCH)
    Disease:

    Familial hypercholesterolemia

  228. JTUi005-A

    China Sixth People's Hospital, Shanghai Jiao Tong University (JTU)
    Disease:

    Neuronal intranuclear inclusion disease

  229. KAIMRCi003-A (DRVT-iPSC#1)

    Saudi Arabia King Abdullah International Medical Research Center (KAIMRC)
    Disease:

    Dravet syndrome

  230. KAUSTi001-B (KS7-iPSC#B)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Klinefelter's syndrome

  231. KAUSTi003-A (KS1-iPSC#D)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Klinefelter's syndrome

  232. KAUSTi004-A (HM-iPSC#A)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Normal (average)

  233. KAUSTi004-B (HM-iPSC#B)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Normal (average)

  234. KAUSTi005-A (HB-iPSC#A)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Normal (average)

  235. KAUSTi005-B (HB-iPSC#B)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Normal (average)

  236. KAUSTi005-C (HB-iPSC#C)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Normal (average)

  237. KAUSTi006-A (KS6-iPSC#A)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Klinefelter's syndrome

  238. KAUSTi006-B (KS6-iPSC#B)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Klinefelter's syndrome

  239. KAUSTi007-A (KS2-iPSC#A)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Klinefelter's syndrome

  240. KAUSTi007-B (KS2-iPSC#B)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Klinefelter's syndrome

  241. KAUSTi008-A (KS4-iPSC#A)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Klinefelter's syndrome

  242. KAUSTi008-B (KS4-iPSC#B)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Klinefelter's syndrome

  243. KAUSTi008-C (KS4-iPSC#C)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Klinefelter's syndrome

  244. KAUSTi008-D (KS4-iPSC#D)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Klinefelter's syndrome

  245. KAUSTi008-E (KS4-iPSC#E)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Klinefelter's syndrome

  246. KAUSTi008-F (KS4-iPSC#F)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Klinefelter's syndrome

  247. KAUSTi008-G (KS4-iPSC#G)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Klinefelter's syndrome

  248. KAUSTi009-A (KS3-iPSC#A)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Klinefelter's syndrome

  249. KAUSTi009-B (KS3-iPSC#B)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Klinefelter's syndrome

  250. KAUSTi010-A (KS5-iPSC#A)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Klinefelter's syndrome

  251. KAUSTi010-B (KS5-iPSC#B)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Klinefelter's syndrome

  252. KAUSTi011-A (iPSC-GLP1R-KO-C1)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Developmental and epileptic encephalopathy

  253. KAUSTi011-B (iPSC-GLP1R-KO-H4)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Developmental and epileptic encephalopathy

  254. WAe001-A-I (H1.0-29/H1.1-13)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Normal (average)

  255. WAe001-A-V (H1.1-39/H1.4-17)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Normal (average)

  256. KCLi001-A (iOP118)

    United Kingdom King's College London (KCL)
    Disease:

    Atopic eczema

  257. KCLi002-A (iOP107)

    United Kingdom King's College London (KCL)
    Disease:

    Atopic eczema

  258. KCLi003-A (iOP101)

    United Kingdom King's College London (KCL)
    Disease:

    Atopic eczema

  259. KEIUi002-A (KOMENT-A)

    Japan Keio University (KEIU)
    Disease:

    Normal (average)

  260. KGUi001-A (AR1023)

    Germany Department of Psychiatry, Psychotherapy and Psychosomatic Medicine, University Hospital, Goethe University of Frankfurt/Main (KGU)
    Disease:

    Obsolete_bipolar disorder

  261. KGUi002-A (AR1034)

    Germany Department of Psychiatry, Psychotherapy and Psychosomatic Medicine, University Hospital, Goethe University of Frankfurt/Main (KGU)
    Disease:

    Obsolete_bipolar disorder

  262. KIe001-A-1

    Sweden Karolinska Institutet (KI)
    Disease:

    Normal (average)

  263. KIe053-A (HS983a)

    Sweden Karolinska Institutet (KI)
    Disease:

    Normal (average)

  264. KLRMMEi001-A

    China Key Laboratory for Regenerative Medicine of Ministry of Education, Jinan University. (KLRMME)
    Disease:

    Retinitis pigmentosa

  265. KLRMMEi003-A

    China Key Laboratory for Regenerative Medicine of Ministry of Education, Jinan University. (KLRMME)
    Disease:

    Usher syndrome

  266. KRIBBi009-A (KRIBB-BC15)

    South Korea Korea Research Institute of Bioscience and Biotechnology (KRIBB)
    Disease:

    Normal (average)

  267. WAe009-A-95 (hTRF1-KO #3)

    South Korea Korea Research Institute of Bioscience and Biotechnology (KRIBB)
    Disease:

    Normal (average)

  268. WAe009-A-96 (hTRF1-KO #6)

    South Korea Korea Research Institute of Bioscience and Biotechnology (KRIBB)
    Disease:

    None

  269. KSCBi005-A (CMC-hiPSC-003)

    South Korea National Stem Cell Bank (KSCB)
    Disease:

    Normal (average)

  270. KSCBi006-A (KNIH-OI001i-A)

    South Korea National Stem Cell Bank (KSCB)
    Disease:

    Osteogenesis imperfecta type 1

  271. BIONi010-C-56 (BIONi010-C-A713T-C25)

    Denmark University of Copenhagen (KU)
    Disease:

    Epilepsy

  272. BIONi010-C-57 (BIONi010-C-A713T-C42)

    Denmark University of Copenhagen (KU)
    Disease:

    Epilepsy

  273. BIONi010-C-58 (BIONi010-C-A713T-C1)

    Denmark University of Copenhagen (KU)
    Disease:

    Epilepsy

  274. BIONi010-C-59 (BIONi010-C-A713T-C33)

    Denmark University of Copenhagen (KU)
    Disease:

    Epilepsy

  275. BIONi010-C-60 (BIONi010-C-R589C-C7)

    Denmark University of Copenhagen (KU)
    Disease:

    Epilepsy

  276. BIONi010-C-61 (BIONi010-C-R589C-C16)

    Denmark University of Copenhagen (KU)
    Disease:

    Epilepsy

  277. BIONi010-C-62 (BIONi010-C-R589C-C5)

    Denmark University of Copenhagen (KU)
    Disease:

    Epilepsy

  278. BIONi010-C-63 (BIONi010-C-R589C-C9)

    Denmark University of Copenhagen (KU)
    Disease:

    Epilepsy

  279. KUi012-A-1 (JM09 GC)

    Denmark University of Copenhagen (KU)
    Disease:

    Epilepsy

  280. KUi013-A-1 (SK GC)

    Denmark University of Copenhagen (KU)
    Disease:

    Epilepsy

  281. KUMi001-A (KUMi001-A_CML(Ph+))

    South Korea Korea University Medical School Hospital (KUM)
    Disease:

    Myeloid leukemia, philadelphia-positive

  282. KUMi002-A (CD34+ CML (Ph-) hiPSCs)

    South Korea Korea University Medical School Hospital (KUM)
    Disease:

    Chronic myeloid leukemia

  283. KUMi004-A

    South Korea Korea University Medical School Hospital (KUM)
    Disease:

    Chronic lymphocytic leukemia

  284. KUMi005-A

    South Korea Korea University Medical School Hospital (KUM)
    Disease:

    Multiple myeloma

  285. KUMi006-A

    South Korea Korea University Medical School Hospital (KUM)
    Disease:

    Multiple myeloma

  286. KUMCi001-A (ALLCD34+)

    South Korea KOREA UNIVERSTY COLLEGE OF MEDICINE (KUMC)
    Disease:

    Acute lymphoblastic leukemia

  287. KUMCi002-A (MM_CD34+iPSCs)

    South Korea KOREA UNIVERSTY COLLEGE OF MEDICINE (KUMC)
    Disease:

    Multiple myeloma

  288. LCPHi001-A

    China The Institute for Tissue Engineering and Regenerative Medicine, Liaocheng People's Hospital (LCPH)
    Disease:

    Obsolete_parkinson's disease

  289. LCPHi003-A

    China The Institute for Tissue Engineering and Regenerative Medicine, Liaocheng People's Hospital (LCPH)
    Disease:

    Parkinson disease

  290. LUMCi029-A (LUMC0072iCTRL01)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Normal (average)

  291. LUMCi029-B (LUMC0004iCTRL10)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Normal (average)

  292. LUMCi039-A (LQT1-1781G/A hiPSC and LUMC0021iKCNQ-30)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Long qt syndrome 1

  293. LUMCi054-A (CRB1 patient c.3122T>C p.(Met1041Thr) homozygote and LUMC0116iCRB09)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Retinitis pigmentosa

  294. LUMCi054-A-1 (LUMC0116iCRB09 ISO-02, LUMC0116iCRB09 homozygote CRISPR corrected isogenic clone 02 and iso02LUMC0116iCRB09)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Retinitis pigmentosa

  295. LUMCi054-A-2 (LUMC0116iCRB09 ISO-03, LUMC0116iCRB09 heterozygote CRISPR corrected isogenic clone 03 and iso03LUMC0116iCRB09)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Retinitis pigmentosa

  296. LUMCi055-A (CRB1 patient 117 compound heterozygous 2983G>T p.(Glu995*) c.1892A>G, p.(Tyr631Cys) and LUMC0117iCRB01)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Retinitis pigmentosa

  297. LUMCi056-A (CRB1 patient 128 compound heterozygous c.2843G>A p.(Cys948Tyr) and c.3122T>C p.(Met1041Thr) and LUMC0128iCRB01)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Retinitis pigmentosa

  298. LUMCi056-A-1 (LUMC0128iCRB01 heterozygote CRISPR corrected isogenic clone 02 and iso02LUMC0128iCRB01)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Retinitis pigmentosa

  299. MCRIi001-A-1 (PB001-OI26)

    Australia Murdoch Children's Research Institute (MCRI)
    Disease:

    Osteogenesis imperfecta

  300. MDCi008-A (8993-B12)

    Germany Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Leigh disease

  301. MDCi009-A (8993-C11)

    Germany Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Leigh disease

  302. MILi001-A (K10 and hFF-iPSCs)

    Germany Miltenyi Biotec B.V. & Co. KG (MIL)
    Disease:

    Normal (average)

  303. MILi001-B (F5)

    Germany Miltenyi Biotec B.V. & Co. KG (MIL)
    Disease:

    Normal (average)

  304. MILi001-C (F10)

    Germany Miltenyi Biotec B.V. & Co. KG (MIL)
    Disease:

    Normal (average)

  305. MLUi001-M

    Germany Medical Faculty of the Martin Luther University Halle-Wittenberg (MLU)
    Disease:

    Schizophrenia

  306. MLUi002-G

    Germany Medical Faculty of the Martin Luther University Halle-Wittenberg (MLU)
    Disease:

    Schizophrenia

  307. MMCi001-A (MMC-iPSC-052B-02)

    Taiwan Mackay Medical College (MMC)
    Disease:

    Deafness, autosomal recessive 1a

  308. MNZTASi034-A (MS_0034.1)

    Australia Menzies Institute for Medical Research (MNZTAS)
    Disease:

    Normal (average)

  309. MPIi002-A (T4 and L1-1Mut)

    Germany Max Planck Institute for Molecular Biomedicine (MPI)
    Disease:

    Obsolete_parkinson's disease

  310. MRIi018-A (HLHS_375)

    Germany Klinikum rechts der Isar (MRI)
    Disease:

    Hypoplastic left heart syndrome

  311. MRIi024-A (Shox2.2)

    Germany Klinikum rechts der Isar (MRI)
    Disease:

    Atrial fibrillation

  312. MSKi002-A (C27 and iPS-27)

    United States Memorial Sloan Kettering Cancer Center (MSK)
    Disease:

    Normal (average)

  313. WAe009-A-1J (H9::mcherry cyto-reporter line)

    United States Memorial Sloan Kettering Cancer Center (MSK)
    Disease:

    Normal (average)

  314. WAe009-A-1W (H9 EF1A-mCherry-noPuro 803_AAVS-iSHH #3)

    United States Memorial Sloan Kettering Cancer Center (MSK)
    Disease:

    Normal (average)

  315. MUi010-A (MYH9)

    Thailand Mahidol University (MU)
    Disease:

    Myh9-related disease

  316. MUi015-A (RB1)

    Thailand Mahidol University (MU)
    Disease:

    Retinoblastoma

  317. MUBi002-A (CF 001)

    Poland Medical University of Bialystok (MUB)
    Disease:

    Cystic fibrosis

  318. MURAi003-A (HoHLA, Homozygous-HLA and HoHLA C3)

    Thailand Faculty of Medicine Ramathibodi Hospital (MURA)
    Disease:

    Normal (average)

  319. MUSIi001-A-2 (HLA-I/II-null SFiPSCs)

    Thailand Faculty of Medicine Siriraj Hospital (MUSI)
    Disease:

    Normal (average)

  320. MUSIi016-A (TyO)

    Thailand Faculty of Medicine Siriraj Hospital (MUSI)
    Disease:

    Normal (average)

  321. NCHi003-A (NCH005)

    United States Nationwide Children's Hospital (NCH)
    Disease:

    Pulmonary valve atresia with intact ventricular septum

  322. NCHi006-A (NCH023)

    United States Nationwide Children's Hospital (NCH)
  323. NCHi013-A (NCH17)

    United States Nationwide Children's Hospital (NCH)
    Disease:

    Pulmonary valve atresia with intact ventricular septum

  324. NCHi014-A (NCH3-N1HET)

    United States Nationwide Children's Hospital (NCH)
    Disease:

    Normal (average)

  325. NCHi015-A (NCH178)

    United States Nationwide Children's Hospital (NCH)
    Disease:

    Type i truncus arteriosus

  326. NCHi023-A (NCH217)

    United States Nationwide Children's Hospital (NCH)
    Disease:

    Nemaline myopathy

  327. WAe001-A-65

    China Nanfang Hospital, Southern Medical University (NFYY)
    Disease:

    Epileptic encephalopathy

  328. NIHTVBi028-A

    United States National Institutes of Health-National Heart, Lung, and Blood Institute (NIHTVB)
    Disease:

    Lyn gene mutation

  329. NIHTVBi029-A (HT1127A (NIHTVBi029-A))

    United States National Institutes of Health-National Heart, Lung, and Blood Institute (NIHTVB)
    Disease:

    Cdc42

  330. NIHTVBi030-A (HT1128A (NIHTVBi030-A))

    United States National Institutes of Health-National Heart, Lung, and Blood Institute (NIHTVB)
    Disease:

    Cdc42 gene

  331. NIHTVBi031-A (HT1129D)

    United States National Institutes of Health-National Heart, Lung, and Blood Institute (NIHTVB)
    Disease:

    Autoimmune interstitial lung, joint, and kidney disease

  332. TMOi001-A-5 (DISC1 Ex2 D5)

    Germany NMI Natural and Medical Sciences Institute at the University of Tübingen (NMI)
    Disease:

    Normal (average)

  333. NMIi010-A

    Germany NMI Natural and Medical Sciences Institute at the University of Tübingen (NMI)
    Disease:

    Normal (average)

  334. NMIi011-A (B1.4)

    Germany NMI Natural and Medical Sciences Institute at the University of Tübingen (NMI)
    Disease:

    Breast carcinoma

  335. NMIi011-B (B1.6)

    Germany NMI Natural and Medical Sciences Institute at the University of Tübingen (NMI)
    Disease:

    Breast carcinoma

  336. NMIi011-C (B1.7)

    Germany NMI Natural and Medical Sciences Institute at the University of Tübingen (NMI)
    Disease:

    Breast carcinoma

  337. NMIi011-D (B1.10)

    Germany NMI Natural and Medical Sciences Institute at the University of Tübingen (NMI)
    Disease:

    Breast carcinoma

  338. NSi003-A (NSi-DS)

    India Stem Cell and Neurobiology Lab (NS)
    Disease:

    Down syndrome

  339. NSi003-B (NSi-isoEu)

    India Stem Cell and Neurobiology Lab (NS)
    Disease:

    Down syndrome

  340. NTUHi002-A

    Taiwan National Taiwan University Hospital (NTUH)
    Disease:

    Aceruloplasminemia

  341. NTUHi004-A

    Taiwan National Taiwan University Hospital (NTUH)
    Disease:

    Leigh syndrome

  342. NTUHi005-A (IBMS-iPSC-071-01)

    Taiwan National Taiwan University Hospital (NTUH)
  343. NUIGi001-A (iPSC ARO1-11)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Autosomal recessive osteopetrosis

  344. OTATi001-A (HC4)

    United States Office of Tissues and Advanced Therapies, CBER, FDA (OTAT)
    Disease:

    Normal (average)

  345. PCIi029-A (PC076)

    France PHENOCELL (PCI)
    Disease:

    Waardenburg syndrome type 1

  346. PCIi030-A (PC078)

    France PHENOCELL (PCI)
    Disease:

    Waardenburg syndrome type 1

  347. PCIi031-A (PC079)

    France PHENOCELL (PCI)
    Disease:

    Waardenburg syndrome type 1

  348. PEIi021-A (PEIi004-A)

    Germany Paul-Ehrlich-Institut (PEI)
    Disease:

    Leukocyte adhesion deficiency type 1

  349. PEIi022-A (PEIi005-A)

    Germany Paul-Ehrlich-Institut (PEI)
    Disease:

    Leukocyte adhesion deficiency type 1

  350. PFIZi001-A (EM1-3F)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Primary erythromelalgia

  351. RCi001-A (Thp3C-6 and RCi88)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Primary erythromelalgia

  352. RCi001-B (RCi89 and Thp3C-9)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Primary erythromelalgia

  353. RCi002-A (FP5C-14 and RCi92)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Primary erythromelalgia

  354. RCi002-B (FP5C-16 and RCi93)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Primary erythromelalgia

  355. RCi003-A (RCi115 and CIP11A-5)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Pain agnosia

  356. RCi003-B (CIP11A-9 and RCi117)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Pain agnosia

  357. PNUSCRi001-A (GBA PD iPSC7)

    South Korea Pusan National University: Convergence Stem Cell Research Center (PNUSCR)
    Disease:

    Parkinson disease

  358. PNUSCRi002-A (GBA PD iPSC9)

    South Korea Pusan National University: Convergence Stem Cell Research Center (PNUSCR)
    Disease:

    Parkinson disease

  359. PNUSCRi003-A (GBA Gaucher iPSC1)

    South Korea Pusan National University: Convergence Stem Cell Research Center (PNUSCR)
    Disease:

    Gaucher disease

  360. PNUSCRi004-A (GBA PD iPSC8)

    South Korea Pusan National University: Convergence Stem Cell Research Center (PNUSCR)
    Disease:

    Parkinson disease

  361. PNUSCRi005-A

    South Korea Pusan National University: Convergence Stem Cell Research Center (PNUSCR)
    Disease:

    Hunter syndrome

  362. WAe009-A-47

    China Peking University Third Hospital Department of Cardiology (PUHT)
    Disease:

    Cytochrome-c oxidase deficiency disease

  363. PUMCHi020-A

    China Peking Union Medical College Hospital (PUMCH)
    Disease:

    Aicardi-goutieres syndrome

  364. RCi004-A (PDSC-10 and RCi150)

    United Kingdom Roslin Cells (RC)
    Disease:

    Huntington disease

  365. RCe020-A (RC-16 and RC16)

    United Kingdom Roslin Cells (RC)
    Disease:

    Normal (average)

  366. RCMGi001-A (P1L5)

    Russia Research Centre for Medical Genetics (RCMG)
    Disease:

    Cystic fibrosis

  367. RCMGi002-A (P7L2)

    Russia Research Centre for Medical Genetics (RCMG)
    Disease:

    Cystic fibrosis

  368. RCMGi004-A (P6L2)

    Russia Research Centre for Medical Genetics (RCMG)
    Disease:

    Cystic fibrosis

  369. RCMGi004-B (P6L8)

    Russia Research Centre for Medical Genetics (RCMG)
    Disease:

    Cystic fibrosis

  370. RCMGi005-A (P5L1)

    Russia Research Centre for Medical Genetics (RCMG)
    Disease:

    Cystic fibrosis

  371. RCMGi005-B (P5L5)

    Russia Research Centre for Medical Genetics (RCMG)
    Disease:

    Cystic fibrosis

  372. RCMGi011-A (P10L1)

    Russia Research Centre for Medical Genetics (RCMG)
    Disease:

    Mucopolysaccharidosis type ivb

    Disease:

    Autosomal recessive nonsyndromic deafness 12

  373. RCMGi015-A (P16L4)

    Russia Research Centre for Medical Genetics (RCMG)
    Disease:

    Glycogen storage disease i

  374. RCMGi016-A (P17L16)

    Russia Research Centre for Medical Genetics (RCMG)
    Disease:

    Glycogen storage disease i

  375. RCPCMi003-A (ATXN1KCl2)

    Russia Federal State Budgetary Institution Federal Research and Clinical Center of Physical-Chemical Medicine of Federal Medical Biological Agency (RCPCM)
    Disease:

    Spinocerebellar ataxia type 1

  376. RCPCMi004-A (Park14-4)

    Russia Federal State Budgetary Institution Federal Research and Clinical Center of Physical-Chemical Medicine of Federal Medical Biological Agency (RCPCM)
    Disease:

    Obsolete_parkinson's disease

  377. RCPCMi005-A (IPSP12-1)

    Russia Federal State Budgetary Institution Federal Research and Clinical Center of Physical-Chemical Medicine of Federal Medical Biological Agency (RCPCM)
    Disease:

    Obsolete_parkinson's disease

  378. RCPCMi007-A (IPSFF1S)

    Russia Federal State Budgetary Institution Federal Research and Clinical Center of Physical-Chemical Medicine of Federal Medical Biological Agency (RCPCM)
    Disease:

    Normal (average)

  379. RCPCMi008-A (IPS SCA17 sev cln4)

    Russia Federal State Budgetary Institution Federal Research and Clinical Center of Physical-Chemical Medicine of Federal Medical Biological Agency (RCPCM)
    Disease:

    Spinocerebellar ataxia type 17

  380. RCPCMi009-A (IPSRG4S and UEF-3B)

    Finland Federal State Budgetary Institution Federal Research and Clinical Center of Physical-Chemical Medicine of Federal Medical Biological Agency (RCPCM)
    Disease:

    Normal (average)

  381. RCPCMi010-A (iPS 67-7)

    Russia Federal State Budgetary Institution Federal Research and Clinical Center of Physical-Chemical Medicine of Federal Medical Biological Agency (RCPCM)
    Disease:

    X-linked intellectual disability, nascimento type

  382. RCSIi001-A (iPDK)

    Ireland Royal College of Surgeons in Ireland (RCSI)
    Disease:

    Normal (average)

  383. REGUi001-A (IPS4FLV)

    France Institute for Regenerative Medecine & Biotherapy U1183 (REGU)
    Disease:

    Normal (average)

  384. REGUi009-A (myasthenic syndrome due to mutation in ColQ and hiPS 5-9016)

    France Institute for Regenerative Medecine & Biotherapy U1183 (REGU)
    Disease:

    Congenital myasthenic syndrome

  385. RGIe049-A (SI-137)

    United States Reproductive Genetics Institute (RGI)
    Disease:

    Neurofibromatosis

  386. RGIe050-A (SI-138)

    United States Reproductive Genetics Institute (RGI)
    Disease:

    Neurofibromatosis

  387. RGIe051-A (SI-139)

    United States Reproductive Genetics Institute (RGI)
    Disease:

    Neurofibromatosis

  388. RGIe052-A (SI-140)

    United States Reproductive Genetics Institute (RGI)
    Disease:

    Neurofibromatosis

  389. RGIe053-A (SI-141)

    United States Reproductive Genetics Institute (RGI)
    Disease:

    Neurofibromatosis type 1

  390. RGIe134-A (SI-235)

    United States Reproductive Genetics Institute (RGI)
    Disease:

    Neurofibromatosis

  391. RIi005-A (TYR.1.H.iPSC.1)

    Iran Royan Institute (RI)
    Disease:

    Tyrosinemia type 1

  392. KUIFMSi004-A-1 (hPSC MPP8 Neon Green)

    Russia Pirogov Russian National Research Medical University (RNRMU)
    Disease:

    Normal (average)

  393. RUESe001-A (RUES1)

    United States The Rockefeller University (RUES)
    Disease:

    Normal (average)

  394. RUESe002-A-6 (RUES2-GLR)

    United States The Rockefeller University (RUES)
    Disease:

    Normal (average)

  395. SAPi002-A (ALS I, ALS I–FUS-R514S/wt and FUS-R514S/wt)

    Italy Sapienza University of Rome (SAP)
    Disease:

    Amyotrophic lateral sclerosis

  396. SAPi003-A (ALS II, FUS-R521C/wt and ALS II–FUS-R521C/wt)

    Italy Sapienza University of Rome (SAP)
    Disease:

    Amyotrophic lateral sclerosis

  397. SAPi004-A (ALS III, TDP43-A382T/A382T and ALS III-TDP43-A382T/A382T)

    Italy Sapienza University of Rome (SAP)
    Disease:

    Amyotrophic lateral sclerosis

  398. SBWCHi001-A

    China Shenzhen Baoan Women's and Children's Hospital, Jinan University (SBWCH)
    Disease:

    Ctnnb1 gene mutation

  399. SCAUi001-A

    China South China Agricultural University (SCAU)
    Disease:

    Normal (average)

  400. SCHi001-A-1 (AMN5-Corrected iPSC)

    South Korea Severance Children’s Hospital (SCH)
    Disease:

    Adrenoleukodystrophy

  401. SCVIi051-A (477)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Normal (average)

  402. SCVIi053-A (2021)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Normal (average)

  403. SCVIi073-A (SCVIi574C2)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Dilated cardiomyopathy

  404. SCVIi128-A (SCVI766)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Marfan syndrome

  405. SCVIi129-A (SCVI2454)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Marfan syndrome

  406. SDQLCHi061-A

    China Children’s Hospital affiliated to Shandong University (SDQLCH)
    Disease:

    Carbamoyl phosphate synthetase i deficiency disease

  407. SDQLCHi067-A

    China Children’s Hospital affiliated to Shandong University (SDQLCH)
    Disease:

    Subcortical band heterotopia

  408. SDQLCHi068-A

    China Children’s Hospital affiliated to Shandong University (SDQLCH)
    Disease:

    Immunodeficiency 14a, autosomal dominant

  409. SDUe001-A (Odense3)

    Denmark University of Southern Denmark (SDU)
  410. SHEHi002-A (iPS36)

    China Shanghai East Hospital (SHEH)
    Disease:

    Long qt syndrome 8

  411. SMBCi011-A

    China Shandong Medicinal Biotechnology Center (SMBC)
    Disease:

    Prader-willi syndrome

  412. SMUSHi002-A

    China Southern Medical University Shenzhen hospital (SMUSH)
    Disease:

    Normal (average)

  413. SNUe007-A (SNUhES31)

    South Korea Seoul National University (SNU)
    Disease:

    Normal (average)

  414. UOSe012-A-1

    United Kingdom University of Southampton (SOTON)
    Disease:

    Normal (average)

  415. SPHi001-A (SLEi002HZY)

    China Shenzhen People's Hospital (SPH)
    Disease:

    Systemic lupus erythematosus

  416. WAe009-A-48

    China Shenzhen People's Hospital (SPH)
    Disease:

    Long qt syndrome 3

  417. WAe009-A-74

    China Shenzhen People's Hospital (SPH)
    Disease:

    Long qt syndrome 2

  418. WAe009-A-88

    China Shenzhen People's Hospital (SPH)
    Disease:

    Long qt syndrome 2

  419. SPPHIi003-A

    China Sichuan Academy of Medical Science & Sichuan Provincial People’s Hospital (SPPHI)
  420. SUSMi005-A

    United States Stanford University School of Medicine (SUSM)
    Disease:

    Obsolete_parkinson's disease

  421. WAe001-A-81

    China The Seventh Affiliated Hospital (SYSUSH)
    Disease:

    Normal (average)

  422. SZBKi003-A

    China Shenzhen Beike Biotechnology Co., Ltd. (SZBK)
    Disease:

    Normal (average)

  423. SZGJMSi001-A (ZLP-2)

    China Research Center of Biological Psychiatry, Suzhou Guangji hospital (SZGJMS)
    Disease:

    Schizophrenia

  424. SZGJMSi002-A (TSQ-1)

    China Research Center of Biological Psychiatry, Suzhou Guangji hospital (SZGJMS)
    Disease:

    Obsessive-compulsive disorder

  425. SZGJMSi003-A (TSH-2)

    China Research Center of Biological Psychiatry, Suzhou Guangji hospital (SZGJMS)
    Disease:

    Normal (average)

  426. SZGJMSi004-A (WJM-1)

    China Research Center of Biological Psychiatry, Suzhou Guangji hospital (SZGJMS)
    Disease:

    Depression

  427. TCIERi001-A (IER-EK1)

    Taiwan Institute of Eye Research, Hualien Tzu Chi Hospital (TCIER)
    Disease:

    Normal (average)

  428. TMPi014-A (MR030 c1 and MR-030 c1)

    Switzerland Translational Molecular Psychiatry (TMP)
    Disease:

    Attention deficit hyperactivity disorder

  429. TNRMCi001-A (iTAF32)

    Russia Tomsk National Research Medical Center of the Russian Academy of Sciences (TNRMC)
    Disease:

    Cystic fibrosis

  430. TRNDi042-A (HT528A)

    United States NIH/NCATS-TRND Branch (TRND)
    Disease:

    Mucopolysaccharidosis type iiib

  431. TUSMi001-A

    China Tongji University School of Medicine (TUSM)
    Disease:

    Normal (average)

  432. TUSMi002-A

    China Tongji University School of Medicine (TUSM)
    Disease:

    Normal (average)

  433. TUSMi003-A

    China Tongji University School of Medicine (TUSM)
    Disease:

    Alzheimer's disease

  434. TUSMi004-A

    China Tongji University School of Medicine (TUSM)
    Disease:

    Obsessive-compulsive disorder

  435. TUSMi005-A

    China Tongji University School of Medicine (TUSM)
    Disease:

    Obsolete_bipolar disorder

  436. UCLi005-A (LGMD2D Pt. 4 and LGMD2D #4)

    United Kingdom University College London (UCL)
    Disease:

    Limb-girdle muscular dystrophy

  437. UCLi024-A (SMID277 and GOS111B)

    United Kingdom University College London (UCL)
    Disease:

    Argininosuccinic aciduria

  438. WAe001-A-10 (H1_RB1ex3_G3)

    Germany Universität Duisburg-Essen (UDE)
    Disease:

    Retinoblastoma

  439. UGOTSAi002-B (N1-001iC2)

    Sweden The Sahlgrenska Academy at University of Gothenburg (UGOTSA)
    Disease:

    Alzheimer's disease

  440. UGOTSAi003-A (N1-002iC3A)

    Sweden The Sahlgrenska Academy at University of Gothenburg (UGOTSA)
    Disease:

    Alzheimer's disease

  441. UGOTSAi003-B (N1-002iC4)

    Sweden The Sahlgrenska Academy at University of Gothenburg (UGOTSA)
    Disease:

    Alzheimer's disease

  442. UGOTSAi004-A (N1-003iC3)

    Sweden The Sahlgrenska Academy at University of Gothenburg (UGOTSA)
    Disease:

    Alzheimer's disease

  443. UGOTSAi004-B (N1-003iC4)

    Sweden The Sahlgrenska Academy at University of Gothenburg (UGOTSA)
    Disease:

    Alzheimer's disease

  444. UGOTSAi005-A (N1-004iC2)

    Sweden The Sahlgrenska Academy at University of Gothenburg (UGOTSA)
    Disease:

    Normal (average)

  445. UGOTSAi005-B (N1-004iC6)

    Sweden The Sahlgrenska Academy at University of Gothenburg (UGOTSA)
    Disease:

    Normal (average)

  446. UGOTSAi006-A (N1-005iC1)

    Sweden The Sahlgrenska Academy at University of Gothenburg (UGOTSA)
    Disease:

    Alzheimer's disease

  447. UHi006-A-3 (HEL24.3_IFIH1KO)

    Finland University of Helsinki (UH)
    Disease:

    Type i diabetes mellitus

  448. UIOi001-A (AG27)

    Norway University of Oslo (UIO)
    Disease:

    Normal (average)

  449. UIOi006-A (iPSC APOE4/4: Sporadic AD (Coriell #AG10788, female, Age 87))

    Norway University of Oslo (UIO)
  450. UJSi001-A

    China Jiangsu University (UJS)
    Disease:

    Schizophrenia

  451. UKAi010-A (BM 104-12)

    Germany Universitätsklinikum Aachen (UKA)
    Disease:

    Normal (average)

  452. UKEi001-A (ERC001sv1162)

    Germany University Medical Center Hamburg-Eppendorf (UKE)
    Disease:

    Normal (average)

  453. UKEi001-A-1 (CRYABhom)

    Germany University Medical Center Hamburg-Eppendorf (UKE)
    Disease:

    Desminopathy

  454. UKEi001-B (ERC001sv1352)

    Germany University Medical Center Hamburg-Eppendorf (UKE)
    Disease:

    Normal (average)

  455. UKEi001-C (ERC001sv1355)

    Germany University Medical Center Hamburg-Eppendorf (UKE)
    Disease:

    Normal (average)

  456. UKEi002-A (ERC017sv2575)

    Germany University Medical Center Hamburg-Eppendorf (UKE)
    Disease:

    Normal (average)

  457. UKEi002-C (ERC017sv2596)

    Germany University Medical Center Hamburg-Eppendorf (UKE)
    Disease:

    Normal (average)

  458. UKEi003-A (ERC018sv1583)

    Germany University Medical Center Hamburg-Eppendorf (UKE)
    Disease:

    Normal (average)

  459. UKEi003-B (ERC018sv1590)

    Germany University Medical Center Hamburg-Eppendorf (UKE)
    Disease:

    Normal (average)

  460. UKEi003-C (ERC018sv1634)

    Germany University Medical Center Hamburg-Eppendorf (UKE)
    Disease:

    Normal (average)

  461. HVRDe006-A-1

    United States Universitätsklinikum Erlangen (UKER)
    Disease:

    Coffin-siris syndrome

  462. UKJi001-A (PKP2-hiPSC)

    Germany Universitätsklinikum Jena (UKJ), Klinik für Innere Medizin I (KIM I), Dr. M. Bekhite ELsaied (UKJ)
    Disease:

    Normal (average)

  463. UKJi003-A (hiPSC-FD)

    Germany Universitätsklinikum Jena (UKJ), Klinik für Innere Medizin I (KIM I), Dr. M. Bekhite ELsaied (UKJ)
    Disease:

    Fabry disease

  464. UKJi004-A (hiPSC-WT)

    Germany Universitätsklinikum Jena (UKJ), Klinik für Innere Medizin I (KIM I), Dr. M. Bekhite ELsaied (UKJ)
    Disease:

    Normal (average)

  465. UKJi006-A (PKP2-hiPSC-ARVC)

    Germany Universitätsklinikum Jena (UKJ), Klinik für Innere Medizin I (KIM I), Dr. M. Bekhite ELsaied (UKJ)
    Disease:

    Arrhythmogenic right ventricular cardiomyopathy

  466. UKKi035-B (NP0139-B and NP0139-6C)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Rare hypertrophic cardiomyopathy

  467. UMILi024-A (CTL04)

    Italy University of Milan (UMIL)
    Disease:

    Normal (average)

  468. WAe009-A-37 (H9-GSX2-tTA:GFP)

    Italy University of Milan (UMIL)
    Disease:

    Normal (average)

  469. UNAMi002-A (IFC-UNAM iPD02-S)

    Mexico Instituto de Fisiología Celular, Universidad Nacional Autónoma de México (UNAM)
    Disease:

    Parkinson disease

  470. UNAMi003-A (IFC-UNAM iPD03-PINK1)

    Mexico Instituto de Fisiología Celular, Universidad Nacional Autónoma de México (UNAM)
    Disease:

    Parkinson disease

  471. UNIPDi004-A

    Italy University of Padova (UNIPD)
    Disease:

    Normal (average)

  472. UNIPDi004-B (HDP04)

    Italy University of Padova (UNIPD)
    Disease:

    Normal (average)

  473. UOSe001-A (MasterShef1, MShef1 and MstrShef1)

    United Kingdom University of Sheffield (UOS)
    Disease:

    Normal (average)

  474. UOSe007-A (MstrShef2, MShef2 and MasterShef2)

    United Kingdom University of Sheffield (UOS)
    Disease:

    Normal (average)

  475. UOSe008-A (MstrShef3, MShef3 and MasterShef3)

    United Kingdom University of Sheffield (UOS)
    Disease:

    Normal (average)

  476. UOSe009-A (MstrShef4, MShef4 and MasterShef4)

    United Kingdom University of Sheffield (UOS)
    Disease:

    Normal (average)

  477. UOSe010-A (MstrShef5, MShef5 and MasterShef5)

    United Kingdom University of Sheffield (UOS)
    Disease:

    Normal (average)

  478. UOSe011-A (MstrShef6, MShef6 and MasterShef6)

    United Kingdom University of Sheffield (UOS)
    Disease:

    Normal (average)

  479. UOSe012-A (MstrShef7, MShef7 and MasterShef7)

    United Kingdom University of Sheffield (UOS)
    Disease:

    Normal (average)

  480. UOSe013-A (MstrShef8, MasterShef8 and MShef8)

    United Kingdom University of Sheffield (UOS)
    Disease:

    Normal (average)

  481. UOSe014-A (MasterShef10, MShef10 and MstrShef10)

    United Kingdom University of Sheffield (UOS)
    Disease:

    Normal (average)

  482. UOSe015-A (MasterShef11, MstrShef11 and MShef11)

    United Kingdom University of Sheffield (UOS)
    Disease:

    Normal (average)

  483. UOSe016-A (MasterShef12, MShef12 and MstrShef12)

    United Kingdom University of Sheffield (UOS)
    Disease:

    Normal (average)

  484. UOSe017-A (MasterShef13, MstrShef13 and MShef13)

    United Kingdom University of Sheffield (UOS)
    Disease:

    Normal (average)

  485. UOSe018-A (MasterShef14, MShef14 and MstrShef14)

    United Kingdom University of Sheffield (UOS)
    Disease:

    Normal (average)

  486. UTHSCHi001-A (NDC-AD01)

    United States The University of Texas Health Science Center at Houston (UTHSCH)
    Disease:

    Alzheimer's disease

  487. VIACe001-A-1 (BG01V/hOG)

    United States Novocell, Inc. (VIAC)
  488. WAe001-A (WA01 and H1)

    United States WiCell Research Institute (WA)
    Disease:

    Normal (average)

  489. WAe007-A (H7 and WA07)

    United States WiCell Research Institute (WA)
    Disease:

    Normal (average)

  490. WAe009-A (WA09 and H9)

    United States WiCell Research Institute (WA)
    Disease:

    Normal (average)

  491. WAe013-A (WA13 and H13)

    United States WiCell Research Institute (WA)
  492. WAe014-A (WA14 and H14)

    United States WiCell Research Institute (WA)
  493. WIBRe001-A-2 (WIBR3 Oct4-2A-GFP)

    United States Whitehead Institute for Biomedical Research (WIBR)
    Disease:

    Normal (average)

  494. WIBRe004-A (WIN1 and Whitehead Institute Naive Human 1)

    United States Whitehead Institute for Biomedical Research (WIBR)
    Disease:

    Normal (average)

  495. WTSIi001-A (HPSI1213i-pahc_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  496. WTSIi037-A (HPSI0114i-zoxy_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  497. WTSIi038-A (HPSI1113i-ieki_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  498. WTSIi046-B (HPSI0214i-wibj_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  499. WTSIi047-B (HPSI0814i-bokz_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  500. WTSIi049-A (HPSI0514i-wiii_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  501. WTSIi049-B (HPSI0514i-wiii_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  502. WTSIi052-A (HPSI1114i-ziyn_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  503. WTSIi053-A (HPSI0413i-corn_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  504. WTSIi054-B (HPSI0413i-nudd_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  505. WTSIi056-A (HPSI0513i-dipe_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  506. WTSIi057-B (HPSI0513i-giuf_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  507. WTSIi059-A (HPSI0513i-uilw_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  508. WTSIi063-A (HPSI0613i-aevs_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  509. WTSIi068-B (HPSI0613i-giuo_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  510. WTSIi069-A (HPSI0613i-hegp_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  511. WTSIi073-A (HPSI0314i-sojd_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  512. WTSIi082-A (HPSI1013i-cups_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  513. WTSIi083-A (HPSI1213i-xuja_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  514. WTSIi085-A (HPSI1113i-eofe_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  515. WTSIi086-A (HPSI0913i-coyi_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  516. WTSIi098-A (HPSI1213i-nekd_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  517. WTSIi102-A (HPSI0413i-iakz_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  518. WTSIi102-B (HPSI0413i-iakz_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  519. WTSIi103-A (HPSI1213i-nusw_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  520. WTSIi104-A (HPSI0513i-coio_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  521. WTSIi104-B (HPSI0513i-coio_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  522. WTSIi105-A (HPSI0313i-airc_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  523. WTSIi105-B (HPSI0313i-airc_66)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  524. WTSIi106-B (HPSI0613i-hikj_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  525. WTSIi109-A (HPSI0413i-coxy_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  526. WTSIi109-B (HPSI0413i-coxy_33)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  527. WTSIi110-A (HPSI0713i-darw_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  528. WTSIi111-A (HPSI0513i-euir_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  529. WTSIi112-A (HPSI0613i-funp_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  530. WTSIi114-A (HPSI0513i-golb_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  531. WTSIi115-A (HPSI0513i-iasn_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  532. WTSIi116-A (HPSI0813i-iicq_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  533. WTSIi117-A (HPSI0613i-liun_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  534. WTSIi118-A (HPSI0813i-meqo_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  535. WTSIi119-A (HPSI0613i-oefg_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  536. WTSIi120-A (HPSI0513i-oeoo_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  537. WTSIi121-A (HPSI0413i-ougl_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  538. WTSIi121-B (HPSI0413i-ougl_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  539. WTSIi122-A (HPSI0413i-peop_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  540. WTSIi123-A (HPSI0713i-qimz_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  541. WTSIi124-A (HPSI0713i-ruyv_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  542. WTSIi124-B (HPSI0713i-ruyv_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  543. WTSIi125-A (HPSI0413i-uahf_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  544. WTSIi126-A (HPSI0913i-vopm_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  545. WTSIi127-A (HPSI0413i-xekf_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  546. WTSIi128-A (HPSI0413i-yuze_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  547. WTSIi129-A (HPSI0613i-zisa_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  548. WTSIi130-A (HPSI0713i-aehn_22)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  549. WTSIi131-A (HPSI0513i-aipt_33)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  550. WTSIi133-A (HPSI0713i-dard_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  551. WTSIi133-B (HPSI0713i-dard_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  552. WTSIi134-B (HPSI0513i-dulv_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  553. WTSIi137-A (HPSI0613i-lizq_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  554. WTSIi137-B (HPSI0613i-lizq_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  555. WTSIi138-A (HPSI0414i-mita_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  556. WTSIi139-A (HPSI1113i-oaaz_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  557. WTSIi140-A (HPSI0613i-oomz_22)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  558. WTSIi141-A (HPSI0613i-qanu_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  559. WTSIi142-A (HPSI0613i-qony_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  560. WTSIi144-A (HPSI0114i-wegi_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  561. WTSIi145-A (HPSI0813i-wots_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  562. WTSIi146-A (HPSI0613i-xosg_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  563. WTSIi168-A (HPSI0214i-poih_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  564. WTSIi168-B (HPSI0214i-poih_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  565. WTSIi169-A (HPSI0614i-miaj_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  566. WTSIi170-B (HPSI1213i-tolg_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  567. WTSIi171-A (HPSI0914i-zerv_7)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  568. WTSIi171-B (HPSI0914i-zerv_8)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  569. WTSIi172-A (HPSI0914i-laey_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  570. WTSIi172-B (HPSI0914i-laey_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  571. WTSIi173-A (HPSI0414i-naju_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  572. WTSIi174-A (HPSI0614i-paab_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  573. WTSIi175-A (HPSI1014i-tixi_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  574. WTSIi176-B (HPSI0714i-iudw_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  575. WTSIi177-A (HPSI0414i-xojn_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  576. WTSIi178-B (HPSI0215i-fawm_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  577. WTSIi179-A (HPSI0314i-wigw_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  578. WTSIi180-A (HPSI0514i-puie_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  579. WTSIi180-B (HPSI0514i-puie_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  580. WTSIi181-A (HPSI0514i-rutc_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  581. WTSIi182-A (HPSI0614i-kegd_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  582. WTSIi183-A (HPSI0414i-oaqd_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  583. WTSIi183-B (HPSI0414i-oaqd_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  584. WTSIi184-A (HPSI1014i-qayj_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  585. WTSIi184-B (HPSI1014i-qayj_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  586. WTSIi186-A (HPSI1014i-babz_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  587. WTSIi187-A (HPSI1013i-sita_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  588. WTSIi188-A (HPSI1014i-kefb_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  589. WTSIi189-A (HPSI1014i-quls_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  590. WTSIi190-A (HPSI0914i-kajh_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  591. WTSIi191-A (HPSI0215i-oilg_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  592. XACHi004-A

    China Xi'an children's hospital (XACH)
    Disease:

    Atrial fibrillation

  593. XXMUFAi001-A

    China The First Affiliated Hospital of Xinxiang Medical University (XXMUFA)
    Disease:

    Long qt syndrome 2

  594. YBLi004-A (YBL/SH/2018/0062)

    India Yashraj Biotechnology ltd Navi Mumbai India (YBL)
    Disease:

    Normal (average)

  595. YBLi005-A (YBL/OS/2021/00196)

    India Yashraj Biotechnology ltd Navi Mumbai India (YBL)
    Disease:

    Normal (average)

  596. YBLi006-A (YBL/PH/2022/0025)

    India Yashraj Biotechnology ltd Navi Mumbai India (YBL)
  597. YUCMi020-A

    South Korea Yonsei University College of Medicine (YUCM)
    Disease:

    Normal (average)

  598. ZJSHi001-A (ZJSHi-KCNB1)

    China Department of Pediatrics, The Second Affiliated Hospital of Zhejiang University School of Medicine (ZJSH)
    Disease:

    Developmental and epileptic encephalopathy, 26

  599. WAe009-A-B

    China Zhengzhou Central Hospital Affiliated (ZZCH)
    Disease:

    Heart failure

  600. ZZUNEUi010-A (CMF001-A)

    China ZhengZhou University- The first affiliated hospital(ZZU) (ZZUNEU)
    Disease:

    Juvenile amyotrophic lateral sclerosis

  601. ZZUNEUi026-A

    China ZhengZhou University- The first affiliated hospital(ZZU) (ZZUNEU)
    Disease:

    Hypertrophic cardiomyopathy

  602. WAe009-A-C

    China The Second Affiliated Hospital (ZZUSA)
    Disease:

    Heart failure