Search results
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WIBRe001-A-43 (WIBR3_GBA1_IVS2_Het_10C2F)
2 us United States Albert Einstein College of Medicine (AECM)Disease:
Parkinson disease
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WIBRe001-A-44 (WIBR3_GBA1_IVS2_Het_10D11A)
2 us United States Albert Einstein College of Medicine (AECM)Disease:
Parkinson disease
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WIBRe001-A-49 (WIBR3_ATP13A2_FS_Homo_12_6)
2 us United States Albert Einstein College of Medicine (AECM)Disease:
Parkinson disease
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WIBRe001-A-50 (WIBR3_ATP13A2_FS_Homo_12_2)
2 us United States Albert Einstein College of Medicine (AECM)Disease:
Parkinson disease
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WIBRe001-A-51 (WIBR3_ATP13A2_FS_Homo_ 6_1)
2 us United States Albert Einstein College of Medicine (AECM)Disease:
Parkinson disease
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WIBRe001-A-52 (WIBR3_ATP13A2_FS_ 5_6)
2 us United States Albert Einstein College of Medicine (AECM)Disease:
Parkinson disease
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WIBRe001-A-53 (WIBR3_ATP13A2_FS_Homo_2_5)
2 us United States Albert Einstein College of Medicine (AECM)Disease:
Parkinson disease
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WIBRe001-A-54 (WIBR3_VPS13C_FS_Homo_E10-2)
2 us United States Albert Einstein College of Medicine (AECM)Disease:
Parkinson disease
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WIBRe001-A-58 (WIBR3_VPS13C_FS_Homo_H3-1)
2 us United States Albert Einstein College of Medicine (AECM)Disease:
Parkinson disease
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WAe009-A-36 (JPH2-KO)
2 cn China Anzhen Hospital (ANZHEN)Disease:
Hypertrophic cardiomyopathy
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ASGRCi002-A (F3-3#1 CHR)
1 tw Taiwan Genomics Research Center (ASGRC)Disease:
Type 1 diabetes mellitus
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ASGRCi003-A (F3-4#5 CHR)
1 tw Taiwan Genomics Research Center (ASGRC)Disease:
Type 1 diabetes mellitus
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ATLABi008-A (AT-UC I Normal-iC06)
1 sg Singapore IMCB, Adrian Teo's Lab (ATLAB)Disease:
Normal (average)
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ATLABi009-A (AT-UC I Normal-iC13)
1 sg Singapore IMCB, Adrian Teo's Lab (ATLAB)Disease:
Normal (average)
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BBANTWi012-A-1 (TTN_E48_V4623*)
1 be Belgium Biobank Antwerpen (BBANTW)Disease:
Dilated cardiomyopathy
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BBANTWi012-A-2 (iPSC_FB_F19901C3_TTN_E48_L4612*)
1 be Belgium Biobank Antwerpen (BBANTW)Disease:
Dilated cardiomyopathy
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BCHi007-A (HNDS0005-01 #B)
1 us United States Children's Hospital (BCH)Disease:
Succinic semialdehyde dehydrogenase deficiency
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BCHi009-A (HNDS0002-01 #D)
1 us United States Children's Hospital (BCH)Disease:
Succinic semialdehyde dehydrogenase deficiency
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BCHi009-A-1 (HNDS0002-01 #D CC26 +/+)
1 us United States Children's Hospital (BCH)Disease:
Succinic semialdehyde dehydrogenase deficiency
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BCHi011-A (HNDS0003-01 #F)
1 us United States Children's Hospital (BCH)Disease:
Succinic semialdehyde dehydrogenase deficiency
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BCHi011-A-1 (HNDS0003-01 #F CC39 +/+)
1 us United States Children's Hospital (BCH)Disease:
Succinic semialdehyde dehydrogenase deficiency
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BCHi030-B (HNDS0131-01#I)
1 us United States Children's Hospital (BCH)Disease:
Tuberous sclerosis complex
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BCHi047-A (HNDS0056-02#A)
1 us United States Children's Hospital (BCH)Disease:
Phelan-mcdermid syndrome
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BCMi001-B (M22c8 and HSCC-003iPS-Sc8)
1 us United States Baylor College of Medicine (BCM)Disease:
Normal (average)
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BCRTi002-A (P02-1)
1 de Germany Berlin-Brandenburg Center for Regenerative Therapies (BCRT)Disease:
Fibrodysplasia ossificans progressiva
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BCRTi007-A
1 de Germany Berlin-Brandenburg Center for Regenerative Therapies (BCRT)Disease:
Polycystic kidney disease
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BIHi001-A-1 (iBCRT Cas9v1-3G-Kl.16)
1 de Germany Berlin Institute of Health (BIH)Disease:
Normal (average)
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SIGi001-A-14 (SIGi001-A Bi-Allelic MAPT HA-tag)
1 dk Denmark Bioneer (BION)Disease:
Normal (average)
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SIGi001-A-16 (SIGi001-A-9 Bi-Allelic MAPT HA-tag)
1 dk Denmark Bioneer (BION)Disease:
Frontotemporal dementia
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STBCi006-A-1 (ApoE KO)
1 dk Denmark Bioneer (BION)Disease:
Alzheimer disease
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BIONi010-C-71 (BIONi010-C with an APOE 3/3 genotype with an additional, homozygous christchurch mutation)
1 dk Denmark Bioneer (BION)Disease:
Alzheimer's disease
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BIORTCi001-A (BAiPSC 000 and OSTiFGM2)
1 ng Nigeria Biomedical Science Research and Training Centre (BIORTC)Disease:
Normal (average)
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BUCREMi001-A (iPSC-S6D63H-1-hom)
1 us United States Boston University (BUCREM)Disease:
Lethal brain and heart developmental defects
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WIBRe001-A-4 (WIBR3_PRKN_X3DEL_B1-3)
2 us United States University of California, Berkeley (CAL)Disease:
Parkinson disease
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WIBRe001-A-5 (WIBR3_PRKN_X3DEL_F2-5)
2 us United States University of California, Berkeley (CAL)Disease:
Parkinson disease
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WIBRe001-A-6 (WIBR3_PRKN_X3DEL_H2-2)
2 us United States University of California, Berkeley (CAL)Disease:
Parkinson disease
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WIBRe001-A-10 (WIBR3_FBXO7_FS_A3-1)
2 us United States University of California, Berkeley (CAL)Disease:
Parkinson disease
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WIBRe001-A-15 (WIBR3_DNAJC6_c.801-2 A>G+FS/c.801-2 A>G_G12-2)
2 us United States University of California, Berkeley (CAL)Disease:
Parkinson disease
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WIBRe001-A-16 (WIBR3_DNAJC6_FS/FS_H10-1)
2 us United States University of California, Berkeley (CAL)Disease:
Parkinson disease
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CAMi014-A (A1ATD1)
1 gb United Kingdom University of Cambridge (CAM)Disease:
Alpha-1-antitrypsin deficiency
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CBDTi001-A
1 in India Institute for Stem Cell Science and Regenerative Medicine (CBDT)Disease:
Normal (average)
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CBIGi001-A (AIW002-02)
1 ca Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)Disease:
Normal (average)
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CCMi001-A (DMD1)
1 it Italy Centro Cardiologico Monzino IRCCS (CCM)Disease:
Duchenne muscular dystrophy
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CHCMUi002-A
1 cn China Children's hospital of Chongqing Medical University (CHCMU)Disease:
Chronic granulomatous disease
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CHOCi005-A
1 us United States CHOC Children's (CHOC)Disease:
Gm1 gangliosidosis
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WAe001-A-2I (H1 INS-PPImNG and CHOPe004-A-2I)
2 us United States The Children's Hospital of Philadelphia (CHOP)Disease:
Normal (average)
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CHUVi001-A
1 ch Switzerland Centre Hospitalier Universitaire Vaudois (CHUV)Disease:
Normal (average)
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CIGLi001-A (RPChiPS8023G1, iPSC TBX4 WT, StemRNA™ Human iPSC 802-3G and SYNTHEGO 802-30F)
1 us United States Center for Infection and Genomics of the Lung (CIGL)Disease:
Normal (average)
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CIRMi285-A (CW70022)
1 us United States California Institute for Regenerative Medicine (CIRM)Disease:
Diabetic retinopathy
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CIRMi286-A (CW70028)
1 us United States California Institute for Regenerative Medicine (CIRM)Disease:
Type 1 diabetes mellitus
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CIRMi287-A (CW70029)
1 us United States California Institute for Regenerative Medicine (CIRM)Disease:
Type 1 diabetes mellitus
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CIRMi292-A (CW70035)
1 us United States California Institute for Regenerative Medicine (CIRM)Disease:
Diabetic retinopathy
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CIRMi293-A (CW70036)
1 us United States California Institute for Regenerative Medicine (CIRM)Disease:
Diabetic retinopathy
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CIRMi294-A (CW70037)
1 us United States California Institute for Regenerative Medicine (CIRM)Disease:
Type 1 diabetes mellitus
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CIRMi307-A (CW70052)
1 us United States California Institute for Regenerative Medicine (CIRM)Disease:
Type 1 diabetes mellitus
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CIRMi314-A (CW70064)
1 us United States California Institute for Regenerative Medicine (CIRM)Disease:
Diabetic retinopathy
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CIRMi323-A (CW70085)
1 us United States California Institute for Regenerative Medicine (CIRM)Disease:
Diabetic retinopathy
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CIRMi329-A (CW70091)
1 us United States California Institute for Regenerative Medicine (CIRM)Disease:
Diabetic retinopathy
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CIRMi361-A (CW70129)
1 us United States California Institute for Regenerative Medicine (CIRM)Disease:
Diabetic retinopathy
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CIRMi373-A (CW70143)
1 us United States California Institute for Regenerative Medicine (CIRM)Disease:
Type 1 diabetes mellitus
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CIRMi419-A (CW70208)
1 us United States California Institute for Regenerative Medicine (CIRM)Disease:
Type 1 diabetes mellitus
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CIRMi451-A (CW70254)
1 us United States California Institute for Regenerative Medicine (CIRM)Disease:
Type 1 diabetes mellitus
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CIRMi484-A (CW70296)
1 us United States California Institute for Regenerative Medicine (CIRM)Disease:
Diabetic retinopathy
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CIRMi498-A (CW70313)
1 us United States California Institute for Regenerative Medicine (CIRM)Disease:
Diabetic retinopathy
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CIRMi499-A (CW70314)
1 us United States California Institute for Regenerative Medicine (CIRM)Disease:
Type 1 diabetes mellitus
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CIRMi505-A (CW70320)
1 us United States California Institute for Regenerative Medicine (CIRM)Disease:
Type 1 diabetes mellitus
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CIRMi511-A (CW70326)
1 us United States California Institute for Regenerative Medicine (CIRM)Disease:
Diabetic retinopathy
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CIRMi526-A (CW70350)
1 us United States California Institute for Regenerative Medicine (CIRM)Disease:
Type 1 diabetes mellitus
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CIRMi528-A (CW70353)
1 us United States California Institute for Regenerative Medicine (CIRM)Disease:
Type 1 diabetes mellitus
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CIRMi538-A (CW70369)
1 us United States California Institute for Regenerative Medicine (CIRM)Disease:
Type 1 diabetes mellitus
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CIRMi03Z-A (CW30461)
1 us United States California Institute for Regenerative Medicine (CIRM)Disease:
Dilated cardiomyopathy
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CMGANTi003-A (SEMD1)
1 be Belgium Center of Medical Genetics Antwerp (CMGANT)Disease:
X-linked spondyloepimetaphyseal dysplasia
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CMGANTi004-A (SEMD2)
1 be Belgium Center of Medical Genetics Antwerp (CMGANT)Disease:
X-linked spondyloepimetaphyseal dysplasia
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CMGANTi006-A (SEDC1)
1 be Belgium Center of Medical Genetics Antwerp (CMGANT)Disease:
Spondyloepiphyseal dysplasia congenita
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CMGANTi007-A (SEDC2)
1 be Belgium Center of Medical Genetics Antwerp (CMGANT)Disease:
Spondyloepiphyseal dysplasia congenita
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CMGANTi008-A (iPSC_MFS_FBN1_Fi930129_C8)
1 be Belgium Center of Medical Genetics Antwerp (CMGANT)Disease:
Marfan syndrome
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CRICKi003-A (iFCI002)
1 gb United Kingdom The Francis Crick Institute Limited (CRICK)Disease:
Intellectual disability
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CRICKi004-A (iFCI008)
1 gb United Kingdom The Francis Crick Institute Limited (CRICK)Disease:
Spinal muscular atrophy with lower extremity predominant
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CRICKi005-A (iFCI004)
1 gb United Kingdom The Francis Crick Institute Limited (CRICK)Disease:
Spinal muscular atrophy
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CRICKi006-A (iFCI005)
1 gb United Kingdom The Francis Crick Institute Limited (CRICK)Disease:
Spinal muscular atrophy
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CRICKi007-A (iFCI009)
1 gb United Kingdom The Francis Crick Institute Limited (CRICK)Disease:
Spinal muscular atrophy with lower extremity predominant
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CRICKi008-A (iFCI006 and NH13-0078)
1 gb United Kingdom The Francis Crick Institute Limited (CRICK)Disease:
X-linked centronuclear myopathy
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CRICKi009-A (iFCI012 and iFCI012 CLONE 4)
1 gb United Kingdom The Francis Crick Institute Limited (CRICK)Disease:
Vhl
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CRICKi010-A (iFCI013 and iFCI013 Clone 7)
1 gb United Kingdom The Francis Crick Institute Limited (CRICK)Disease:
Vhl
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CRICKi011-A (iFCI016)
1 gb United Kingdom The Francis Crick Institute Limited (CRICK)Disease:
Young-onset parkinson disease
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CRICKi012-A (iFCI017)
1 gb United Kingdom The Francis Crick Institute Limited (CRICK)Disease:
Young-onset parkinson disease
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CRICKi013-A (iFCI018 Clone 6)
1 gb United Kingdom The Francis Crick Institute Limited (CRICK)Disease:
Von hippel-lindau disease tumor suppressor
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CRICKi014-A (iFCI019 Clone 4)
1 gb United Kingdom The Francis Crick Institute Limited (CRICK)Disease:
Von hippel-lindau disease tumor suppressor
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CRICKi015-A (iFCI020 Clone 1)
1 gb United Kingdom The Francis Crick Institute Limited (CRICK)Disease:
Von hippel-lindau disease tumor suppressor
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CRICKi016-A (iFCI021 Clone 7)
1 gb United Kingdom The Francis Crick Institute Limited (CRICK)Disease:
Lung cancer
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CRICKi017-A (iFCI022 Clone 4)
1 gb United Kingdom The Francis Crick Institute Limited (CRICK)Disease:
Lung cancer
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CRICKi018-A (iKER 12 and iFCI023)
1 gb United Kingdom The Francis Crick Institute Limited (CRICK)Disease:
Normal (average)
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CRICKi019-A (iKER 8 and iFCI024)
1 gb United Kingdom The Francis Crick Institute Limited (CRICK)Disease:
Normal (average)
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CRICKi020-A (iFCI025 and iKER 10)
1 gb United Kingdom The Francis Crick Institute Limited (CRICK)Disease:
Normal (average)
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CRICKi021-A (iFCI007)
1 gb United Kingdom The Francis Crick Institute Limited (CRICK)Disease:
Ullrich congenital muscular dystrophy
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CRICKi022-A (iFCI031)
1 gb United Kingdom The Francis Crick Institute Limited (CRICK)Disease:
Lung cancer
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CRICKi023-A (iFCI032)
1 gb United Kingdom The Francis Crick Institute Limited (CRICK)Disease:
Lung squamous cell carcinoma
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CRTDi001-A (T12.9 and C1-1)
1 de Germany Center for Regenerative Therapies Dresden (CRTD)Disease:
Normal (average)
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CSCIi001-A (niPSC HDF16 and niPSC-16.2b)
1 gb United Kingdom Wellcome Trust - MRC Stem Cell Institute (CSCI)Disease:
Normal (average)
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CSCIi002-A (niPSC HDF75 and niPSC-75.1c2)
1 gb United Kingdom Wellcome Trust - MRC Stem Cell Institute (CSCI)Disease:
Normal (average)
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CSSi001-A (Joub03cl2 and COR419)
1 it Italy Fondazione Casa Sollievo della Sofferenza IRCCS (CSS)Disease:
Joubert syndrome
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CSSi015-A (FC17)
1 it Italy Fondazione Casa Sollievo della Sofferenza IRCCS (CSS)Disease:
Normal (average)
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CSUXHi003-A
1 cn China Xiangya Hospital (CSUXH)Disease:
Waardenburg syndrome type 2
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CSUXHi004-A
1 cn China Xiangya Hospital (CSUXH)Disease:
Waardenburg syndrome type 1
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CTEFi001-A (CTEF-hiPSC10 and FNUSA-hiPSC10)
1 cz Czech Republic Cell and Tissue Engineering Facility (CTEF)Disease:
Normal (average)
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DMBi001-A-2
1 pl Poland Department of Medical Biotechnology (DMB)Disease:
Normal (average)
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WAe009-A-58 (COL4A5 heterozygote)
2 cn China Dongzhimen Hospital Affiliated to Beijing University of Chinese Medicine (DZMH)Disease:
Alport syndrome
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EDi010-A (RCi136)
1 gb United Kingdom University of Edinburgh (ED)Disease:
Bipolar disorder
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EDi010-B (RCi138)
1 gb United Kingdom University of Edinburgh (ED)Disease:
Bipolar disorder
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EDi011-A (RCi139)
1 gb United Kingdom University of Edinburgh (ED)Disease:
Bipolar disorder
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EDi011-B (RCi140)
1 gb United Kingdom University of Edinburgh (ED)Disease:
Bipolar disorder
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EDi011-C (RCi141)
1 gb United Kingdom University of Edinburgh (ED)Disease:
Bipolar disorder
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EDi018-B (RCi212)
1 gb United Kingdom University of Edinburgh (ED)Disease:
Bipolar disorder
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EDi018-C (RCi213)
1 gb United Kingdom University of Edinburgh (ED)Disease:
Bipolar disorder
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EDi046-A
1 gb United Kingdom University of Edinburgh (ED)Disease:
Normal (average)
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EHTJUi002-A (DF-GMP-ZB11AR-H)
1 cn China East Hospital Affiliated to Tongji University (EHTJU)Disease:
Normal (average)
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EHTJUi004-A (DF-GMP-ZB12AN-I)
1 cn China East Hospital Affiliated to Tongji University (EHTJU)Disease:
Normal (average)
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ESi065-A ([IDDM1] FiPS 1.13-Ep6F-9)
1 es Spain Spanish Stem Cell Bank (ES)Disease:
Obsolete_type i diabetes mellitus
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ESi080-A (N1-FiPS4F#7)
1 es Spain Spanish Stem Cell Bank (ES)Disease:
Normal (average)
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ESi104-A (PMM2-CDG FiPS48-Sv4F-7)
1 es Spain Spanish Stem Cell Bank (ES)Disease:
Pmm2-cdg
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ESi112-A
1 es Spain Spanish Stem Cell Bank (ES)Disease:
Normal (average)
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FDCHDPi001-A (FDCHDP01)
1 cn China Fudan University (FDCHDP)Disease:
Tourette syndrome
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FMMUNIi001-A (I-WT)
1 cz Czech Republic Faculty of Medicine, Masaryk University (FMMUNI)Disease:
Normal (average)
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FMMUNIi002-A (I-IF)
1 cz Czech Republic Faculty of Medicine, Masaryk University (FMMUNI)Disease:
Ventricular fibrillation
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FMMUNIi003-A (I-CPVT)
1 cz Czech Republic Faculty of Medicine, Masaryk University (FMMUNI)Disease:
Catecholaminergic polymorphic ventricular tachycardia
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GENEAe008-A (GENEA009 and SIVF09)
2 au Australia Genea (GENEA) UNKNOWN -
GENEAe013-A (GENEA089)
2 au Australia Genea (GENEA)Disease:
Huntington disease
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GENEAe014-A (GENEA029)
2 us United States Genea (GENEA)Disease:
Normal (average)
-
GENEAe015-A (GENEA020)
2 us United States Genea (GENEA)Disease:
Huntington disease
-
GENEAe017-A (GENEA023)
2 au Australia Genea (GENEA)Disease:
Normal (average)
-
GENEAe018-A (GENEA090)
2 au Australia Genea (GENEA)Disease:
Huntington disease
-
GENEAe019-A (GENEA091)
2 au Australia Genea (GENEA)Disease:
Huntington disease
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GENYOi001-A (PBMC1-iPS4F1)
1 es Spain Centre for Genomics and Oncological Research (GENYO)Disease:
Normal (average)
-
GENYOi003-A (PBMC2-iPS4F8)
1 es Spain Centre for Genomics and Oncological Research (GENYO)Disease:
Normal (average)
-
GENYOi004-A (ASD-PBMC-iPS4F2)
1 es Spain Centre for Genomics and Oncological Research (GENYO)Disease:
Adnp syndrome
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GENYOi005-A (FPD/AML-PBMC-iPSC4F73)
1 es Spain Centre for Genomics and Oncological Research (GENYO)Disease:
Familial platelet disorder with associated myeloid malignancy
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WAe009-A-84
2 cn China Guangxi Institute of Cardiovascular Diseases (GICD)Disease:
Congenital heart disease
-
WAe001-A-2C (SST-P2A-mCherry)
2 cn China Guangzhou Laboratory (GL)Disease:
Normal (average)
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GRCHJUi001-A (LYJ-iPS-C)
1 cn China Guangzhou Red Cross Hospital of Jinan University (GRCHJU)Disease:
Atrial fibrillation
-
HCORDi001-I (M2_IPSC4_P)
1 br Brazil Hemocord Clínica Médica Ltda (HCORD)Disease:
Normal (average)
-
HEBHMUi010-A
1 cn China Hebei Medical University (HEBHMU)Disease:
Normal (average)
-
HELPi001-A (BS-TL-1)
1 cn China Help Stem Cell Innovations Co.Ltd. (HELP)Disease:
Congenital contractural arachnodactyly
-
HHUi003-B (A4_C1)
1 de Germany Universitätsklinikum Düsseldorf (HHU)Disease:
Maternally-inherited leigh syndrome
-
HHUi003-C (A4_W1)
1 de Germany Universitätsklinikum Düsseldorf (HHU)Disease:
Maternally-inherited leigh syndrome
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HHUi006-A (11656_H)
1 de Germany Universitätsklinikum Düsseldorf (HHU)Disease:
Normal (average)
-
HHUi006-B (11656_K)
1 de Germany Universitätsklinikum Düsseldorf (HHU)Disease:
Normal (average)
-
HNMUi009-A (iPS-UC1171)
1 cn China Hainan Medical University (HNMU)Disease:
Thalassemia
-
HVRDi005-A (BJ SiPS-D)
1 us United States Harvard University (HVRD)Disease:
Normal (average)
-
IBBISTi010-A (4_H17)
1 pt Portugal Simão José Teixeira da Rocha (IBBIST)Disease:
Hypertrophic cardiomyopathy
-
IBBISTi011-A (3_H24)
1 pt Portugal Simão José Teixeira da Rocha (IBBIST)Disease:
Hypertrophic cardiomyopathy
-
IBBISTi012-A (6_H35)
1 pt Portugal Simão José Teixeira da Rocha (IBBIST)Disease:
Hypertrophic cardiomyopathy
-
IBBISTi013-A (4_H22)
1 pt Portugal Simão José Teixeira da Rocha (IBBIST)Disease:
Hypertrophic cardiomyopathy
-
IBKMOLi003-A (vEDS COL3A1 Q105* iPSC)
1 at Austria University of Innsbruck, Institute of Molecular Biology (IBKMOL)Disease:
Vascular ehlers-danlos syndrome
-
IBKMOLi004-A (sCeAD iPSC)
1 at Austria University of Innsbruck, Institute of Molecular Biology (IBKMOL) UNKNOWN -
IBKMOLi005-A (CTRL iPSC)
1 at Austria University of Innsbruck, Institute of Molecular Biology (IBKMOL)Disease:
Normal (average)
-
IBPi002-A (P71 iPSCs 1)
1 cz Czech Republic Institute of Biophysics of the Czech Academy of Sciences (IBP)Disease:
Prostate adenocarcinoma
-
ICANi001-A (CDGEN1.16)
1 fr France INSERM U1166-Institute of Cardiometabolism And Nutrition (ICAN)Disease:
Hypertrophic cardiomyopathy
-
ICANi001-A-1 (CDGEN1.16.40.5)
1 fr France INSERM U1166-Institute of Cardiometabolism And Nutrition (ICAN)Disease:
Hypertrophic cardiomyopathy
-
ICANi002-A (ICAN-403.3)
1 fr France INSERM U1166-Institute of Cardiometabolism And Nutrition (ICAN)Disease:
Normal (average)
-
ICANi002-A-1 (ICAN-FLNC42.1)
1 fr France INSERM U1166-Institute of Cardiometabolism And Nutrition (ICAN)Disease:
Normal (average)
-
ICANi002-A-3 (ICAN-BAG3-V468MC34)
1 fr France INSERM U1166-Institute of Cardiometabolism And Nutrition (ICAN)Disease:
Dilated cardiomyopathy 1hh
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ICANi002-A-4 (ICAN_BAG3_M468MC19)
1 fr France INSERM U1166-Institute of Cardiometabolism And Nutrition (ICAN)Disease:
Dilated cardiomyopathy 1hh
-
ICANi002-A-5 (ICAN-PKP2-H695-W11)
1 fr France INSERM U1166-Institute of Cardiometabolism And Nutrition (ICAN)Disease:
Arrhythmogenic right ventricular dysplasia 9
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ICGi002-A (DMD1_1)
1 ru Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)Disease:
Duchenne muscular dystrophy
-
ICGi002-B (DMD1_4)
1 ru Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)Disease:
Duchenne muscular dystrophy
-
ICGi002-C (DMD1_11)
1 ru Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)Disease:
Duchenne muscular dystrophy
-
ICGi003-A (f3SMA3)
1 ru Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)Disease:
Spinal muscular atrophy type 3
-
ICGi005-A (iSMA40)
1 ru Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)Disease:
Proximal spinal muscular atrophy type 1
-
ICGi005-B (iSMA37)
1 ru Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)Disease:
Proximal spinal muscular atrophy type 1
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ICGi006-A (m3SMA13)
1 ru Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)Disease:
Proximal spinal muscular atrophy type 2
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ICGi006-B (m3SMA20)
1 ru Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)Disease:
Proximal spinal muscular atrophy type 2
-
ICGi007-A (47Q-3Lf)
1 ru Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)Disease:
Huntington disease
-
ICGi009-A (iTAF3-17 and iTAF3del17)
1 ru Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)Disease:
Intellectual disability
-
ICGi009-B (iTAF3del37 and iTAF3-37)
1 ru Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)Disease:
Intellectual disability
-
ICGi013-A (iTAF13-26 and iTAF13del26)
1 ru Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)Disease:
Intellectual disability
-
ICGi013-B (iTAF13del27 and iTAF13-27)
1 ru Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)Disease:
Intellectual disability
-
ICGi015-B-1 (m6.7pCyto-17)
1 ru Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)Disease:
Parkinson disease
-
ICGi018-A (iHD38Q-3)
1 ru Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)Disease:
Huntington's disease
-
ICGi018-B (iHD38Q-2)
1 ru Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)Disease:
Huntington's disease
-
ICGi018-C (iHD38Q-1)
1 ru Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)Disease:
Huntington's disease
-
ICGi019-A (HCM1f6)
1 ru Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)Disease:
Hypertrophic cardiomyopathy
-
ICGi019-B (HCM1f33)
1 ru Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)Disease:
Hypertrophic cardiomyopathy
-
ICGi021-A (K6-4f)
1 ru Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)Disease:
Normal (average)
-
ICGi021-A-1 (K6-4fpCyto-13)
1 ru Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)Disease:
Healthy
-
ICGi022-A (K7-4Lf)
1 ru Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)Disease:
Healthy subject
-
ICGi025-A (iTAF11-4)
1 ru Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)Disease:
Developmental delay
-
ICGi028-A (HCM4fm5.2)
1 ru Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)Disease:
Hypertrophic cardiomyopathy
-
ICGi029-A (HCM14fm6.2)
1 ru Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)Disease:
Hypertrophic cardiomyopathy
-
ICGi030-A (HF2)
1 ru Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)Disease:
Wilson disease
-
IDVi006-A (UBAP1L-3225)
1 fr France INSTITUT DE LA VISION (IDV)Disease:
Retinal dystrophy
-
IGIBi002-A
1 in India CSIR-Institute of Genomics and Integrative Biology (IGIB)Disease:
Beta-thalassemia
-
IGIBi019-A (iPSC V2b)
1 in India CSIR-Institute of Genomics and Integrative Biology (IGIB)Disease:
Normal (average)
-
IGIBi020-A (iPSC V1b)
1 in India CSIR-Institute of Genomics and Integrative Biology (IGIB)Disease:
Normal (average)
-
IGIBi021-A (iPSC V3b)
1 in India CSIR-Institute of Genomics and Integrative Biology (IGIB)Disease:
Normal (average)
-
IGIBi022-A (iPSC V2c)
1 in India CSIR-Institute of Genomics and Integrative Biology (IGIB)Disease:
Normal (average)
-
IGIBi023-A (iPSC V1c)
1 in India CSIR-Institute of Genomics and Integrative Biology (IGIB)Disease:
Normal (average)
-
IGIBi024-A (iPSC V3c)
1 in India CSIR-Institute of Genomics and Integrative Biology (IGIB)Disease:
Normal (average)
-
IGIBi025-A (iPSC V3a)
1 in India CSIR-Institute of Genomics and Integrative Biology (IGIB)Disease:
Normal (average)
-
IMBPASi001-A (iPSC-WFS1-#1)
1 pl Poland Institute of Medical Biology of Polish Academy of Sciences (IMBPAS)Disease:
Wolfram syndrome 1
-
IMGTi001-A (iTAF5-29)
1 ru Russia Research Institute of Medical Genetics, TNMRC (IMGT)Disease:
Phelan-mcdermid syndrome
-
INEUi004-A (FHL1-V)
1 ar Argentina Instituto de Neurociencias Conicet (INEU)Disease:
Muscular dystrophy
-
INSAi003-A
1 pt Portugal Instituto Nacional de Saude Ricardo Jorge (INSA)Disease:
Mucolipidosis type ii
-
INSRMi002-A (PC117_c2)
1 fr France INSERM (INSRM)Disease:
Epilepsy
-
INSRMi003-A (PC128_c5)
1 fr France INSERM (INSRM)Disease:
Normal (average)
-
INSRMi004-A (PC118_c7)
1 fr France INSERM (INSRM)Disease:
Epilepsy
-
INSRMi005-A (PC119_c7)
1 fr France INSERM (INSRM)Disease:
Normal (average)
-
INSRMi006-A (PC131_c8)
1 fr France INSERM (INSRM)Disease:
Epilepsy
-
INSRMi007-A (pc132-c4)
1 fr France INSERM (INSRM)Disease:
Normal (average)
-
INSRMe002-A (STR-I-233-FRAXA)
2 fr France INSERM (INSRM)Disease:
Fragile x syndrome
-
INSRMe003-A (STR-I-155-HD)
2 fr France INSERM (INSRM)Disease:
Huntington disease
-
INSRMe004-A (STR-I-171-GLA)
2 fr France INSERM (INSRM)Disease:
Fabry disease
-
INSRMe005-A (STR-I-189-FRAXA)
2 fr France INSERM (INSRM)Disease:
Fragile x syndrome
-
INSRMe006-A (STR-I-209-MEN2a)
2 fr France INSERM (INSRM)Disease:
Endocrine gland cancer
-
INSRMe007-A (STR-I-211-MEN2a)
2 fr France INSERM (INSRM)Disease:
Endocrine gland cancer
-
INSRMe008-A (STR-I-203-CFTR)
2 fr France INSERM (INSRM)Disease:
Cystic fibrosis
-
INSRMe009-A (STR-I-251-CFTR)
2 fr France INSERM (INSRM)Disease:
Cystic fibrosis
-
INSRMe010-A (STR-I-221-Sca2)
2 fr France INSERM (INSRM)Disease:
Autosomal dominant cerebellar ataxia
-
INSRMe011-A (STR-I-229-MTMX)
2 fr France INSERM (INSRM)Disease:
X-linked myopathy with excessive autophagy
-
INSRMe012-A (STR-I-231-MTMX)
2 fr France INSERM (INSRM)Disease:
X-linked myopathy with excessive autophagy
-
INSRMe013-A (STR-I-301-MFS)
2 fr France INSERM (INSRM)Disease:
Marfan syndrome
-
INSRMe014-A (STR-I-305-APC)
2 fr France INSERM (INSRM)Disease:
Familial adenomatous polyposis
-
INSRMe015-A (STR-I-315-CMT1a)
2 fr France INSERM (INSRM)Disease:
Charcot-marie-tooth disease type 1
-
INSRMe016-A (STR-I-347-FRAXA)
2 fr France INSERM (INSRM)Disease:
Fragile x syndrome
-
INSRMe017-A (STR-I-355-APC)
2 fr France INSERM (INSRM)Disease:
Familial adenomatous polyposis
-
INSRMe018-A (STR-I-359-APC)
2 fr France INSERM (INSRM)Disease:
Familial adenomatous polyposis
-
ITXi013-A (PT-R406W)
1 fr France l’institut du thorax (ITX)Disease:
Desminopathy
-
JNCHi002-A (JNCHi002-A)
1 cn China Jinan children's Hospital (JNCH)Disease:
Familial hypercholesterolemia
-
JTUi005-A
1 cn China Sixth People's Hospital, Shanghai Jiao Tong University (JTU)Disease:
Neuronal intranuclear inclusion disease
-
KAIMRCi003-A (DRVT-iPSC#1)
1 sa Saudi Arabia King Abdullah International Medical Research Center (KAIMRC)Disease:
Dravet syndrome
-
KAUSTi001-B (KS7-iPSC#B)
1 sa Saudi Arabia King Abdullah University of Science and Technology (KAUST)Disease:
Klinefelter's syndrome
-
KAUSTi003-A (KS1-iPSC#D)
1 sa Saudi Arabia King Abdullah University of Science and Technology (KAUST)Disease:
Klinefelter's syndrome
-
KAUSTi004-A (HM-iPSC#A)
1 sa Saudi Arabia King Abdullah University of Science and Technology (KAUST)Disease:
Normal (average)
-
KAUSTi004-B (HM-iPSC#B)
1 sa Saudi Arabia King Abdullah University of Science and Technology (KAUST)Disease:
Normal (average)
-
KAUSTi005-A (HB-iPSC#A)
1 sa Saudi Arabia King Abdullah University of Science and Technology (KAUST)Disease:
Normal (average)
-
KAUSTi005-B (HB-iPSC#B)
1 sa Saudi Arabia King Abdullah University of Science and Technology (KAUST)Disease:
Normal (average)
-
KAUSTi005-C (HB-iPSC#C)
1 sa Saudi Arabia King Abdullah University of Science and Technology (KAUST)Disease:
Normal (average)
-
KAUSTi006-A (KS6-iPSC#A)
1 sa Saudi Arabia King Abdullah University of Science and Technology (KAUST)Disease:
Klinefelter's syndrome
-
KAUSTi006-B (KS6-iPSC#B)
1 sa Saudi Arabia King Abdullah University of Science and Technology (KAUST)Disease:
Klinefelter's syndrome
-
KAUSTi007-A (KS2-iPSC#A)
1 sa Saudi Arabia King Abdullah University of Science and Technology (KAUST)Disease:
Klinefelter's syndrome
-
KAUSTi007-B (KS2-iPSC#B)
1 sa Saudi Arabia King Abdullah University of Science and Technology (KAUST)Disease:
Klinefelter's syndrome
-
KAUSTi008-A (KS4-iPSC#A)
1 sa Saudi Arabia King Abdullah University of Science and Technology (KAUST)Disease:
Klinefelter's syndrome
-
KAUSTi008-B (KS4-iPSC#B)
1 sa Saudi Arabia King Abdullah University of Science and Technology (KAUST)Disease:
Klinefelter's syndrome
-
KAUSTi008-C (KS4-iPSC#C)
1 sa Saudi Arabia King Abdullah University of Science and Technology (KAUST)Disease:
Klinefelter's syndrome
-
KAUSTi008-D (KS4-iPSC#D)
1 sa Saudi Arabia King Abdullah University of Science and Technology (KAUST)Disease:
Klinefelter's syndrome
-
KAUSTi008-E (KS4-iPSC#E)
1 sa Saudi Arabia King Abdullah University of Science and Technology (KAUST)Disease:
Klinefelter's syndrome
-
KAUSTi008-F (KS4-iPSC#F)
1 sa Saudi Arabia King Abdullah University of Science and Technology (KAUST)Disease:
Klinefelter's syndrome
-
KAUSTi008-G (KS4-iPSC#G)
1 sa Saudi Arabia King Abdullah University of Science and Technology (KAUST)Disease:
Klinefelter's syndrome
-
KAUSTi009-A (KS3-iPSC#A)
1 sa Saudi Arabia King Abdullah University of Science and Technology (KAUST)Disease:
Klinefelter's syndrome
-
KAUSTi009-B (KS3-iPSC#B)
1 sa Saudi Arabia King Abdullah University of Science and Technology (KAUST)Disease:
Klinefelter's syndrome
-
KAUSTi010-A (KS5-iPSC#A)
1 sa Saudi Arabia King Abdullah University of Science and Technology (KAUST)Disease:
Klinefelter's syndrome
-
KAUSTi010-B (KS5-iPSC#B)
1 sa Saudi Arabia King Abdullah University of Science and Technology (KAUST)Disease:
Klinefelter's syndrome
-
KAUSTi011-A (iPSC-GLP1R-KO-C1)
1 sa Saudi Arabia King Abdullah University of Science and Technology (KAUST)Disease:
Developmental and epileptic encephalopathy
-
KAUSTi011-B (iPSC-GLP1R-KO-H4)
1 sa Saudi Arabia King Abdullah University of Science and Technology (KAUST)Disease:
Developmental and epileptic encephalopathy
-
WAe001-A-I (H1.0-29/H1.1-13)
2 sa Saudi Arabia King Abdullah University of Science and Technology (KAUST)Disease:
Normal (average)
-
WAe001-A-V (H1.1-39/H1.4-17)
2 sa Saudi Arabia King Abdullah University of Science and Technology (KAUST)Disease:
Normal (average)
-
KCLi001-A (iOP118)
1 gb United Kingdom King's College London (KCL)Disease:
Atopic eczema
-
KCLi002-A (iOP107)
1 gb United Kingdom King's College London (KCL)Disease:
Atopic eczema
-
KCLi003-A (iOP101)
1 gb United Kingdom King's College London (KCL)Disease:
Atopic eczema
-
KEIUi002-A (KOMENT-A)
1 jp Japan Keio University (KEIU)Disease:
Normal (average)
-
KGUi001-A (AR1023)
1 de Germany Department of Psychiatry, Psychotherapy and Psychosomatic Medicine, University Hospital, Goethe University of Frankfurt/Main (KGU)Disease:
Obsolete_bipolar disorder
-
KGUi002-A (AR1034)
1 de Germany Department of Psychiatry, Psychotherapy and Psychosomatic Medicine, University Hospital, Goethe University of Frankfurt/Main (KGU)Disease:
Obsolete_bipolar disorder
-
KIe001-A-1
2 se Sweden Karolinska Institutet (KI)Disease:
Normal (average)
-
KIe053-A (HS983a)
2 se Sweden Karolinska Institutet (KI)Disease:
Normal (average)
-
KLRMMEi001-A
1 cn China Key Laboratory for Regenerative Medicine of Ministry of Education, Jinan University. (KLRMME)Disease:
Retinitis pigmentosa
-
KLRMMEi003-A
1 cn China Key Laboratory for Regenerative Medicine of Ministry of Education, Jinan University. (KLRMME)Disease:
Usher syndrome
-
KRIBBi009-A (KRIBB-BC15)
1 kr South Korea Korea Research Institute of Bioscience and Biotechnology (KRIBB)Disease:
Normal (average)
-
WAe009-A-95 (hTRF1-KO #3)
2 kr South Korea Korea Research Institute of Bioscience and Biotechnology (KRIBB)Disease:
Normal (average)
-
WAe009-A-96 (hTRF1-KO #6)
2 kr South Korea Korea Research Institute of Bioscience and Biotechnology (KRIBB)Disease:
None
-
KSCBi005-A (CMC-hiPSC-003)
1 kr South Korea National Stem Cell Bank (KSCB)Disease:
Normal (average)
-
KSCBi006-A (KNIH-OI001i-A)
1 kr South Korea National Stem Cell Bank (KSCB)Disease:
Osteogenesis imperfecta type 1
-
BIONi010-C-56 (BIONi010-C-A713T-C25)
1 dk Denmark University of Copenhagen (KU)Disease:
Epilepsy
-
BIONi010-C-57 (BIONi010-C-A713T-C42)
1 dk Denmark University of Copenhagen (KU)Disease:
Epilepsy
-
BIONi010-C-58 (BIONi010-C-A713T-C1)
1 dk Denmark University of Copenhagen (KU)Disease:
Epilepsy
-
BIONi010-C-59 (BIONi010-C-A713T-C33)
1 dk Denmark University of Copenhagen (KU)Disease:
Epilepsy
-
BIONi010-C-60 (BIONi010-C-R589C-C7)
1 dk Denmark University of Copenhagen (KU)Disease:
Epilepsy
-
BIONi010-C-61 (BIONi010-C-R589C-C16)
1 dk Denmark University of Copenhagen (KU)Disease:
Epilepsy
-
BIONi010-C-62 (BIONi010-C-R589C-C5)
1 dk Denmark University of Copenhagen (KU)Disease:
Epilepsy
-
BIONi010-C-63 (BIONi010-C-R589C-C9)
1 dk Denmark University of Copenhagen (KU)Disease:
Epilepsy
-
KUi012-A-1 (JM09 GC)
1 dk Denmark University of Copenhagen (KU)Disease:
Epilepsy
-
KUi013-A-1 (SK GC)
1 dk Denmark University of Copenhagen (KU)Disease:
Epilepsy
-
KUMi001-A (KUMi001-A_CML(Ph+))
1 kr South Korea Korea University Medical School Hospital (KUM)Disease:
Myeloid leukemia, philadelphia-positive
-
KUMi002-A (CD34+ CML (Ph-) hiPSCs)
1 kr South Korea Korea University Medical School Hospital (KUM)Disease:
Chronic myeloid leukemia
-
KUMi004-A
1 kr South Korea Korea University Medical School Hospital (KUM)Disease:
Chronic lymphocytic leukemia
-
KUMi005-A
1 kr South Korea Korea University Medical School Hospital (KUM)Disease:
Multiple myeloma
-
KUMi006-A
1 kr South Korea Korea University Medical School Hospital (KUM)Disease:
Multiple myeloma
-
KUMCi001-A (ALLCD34+)
1 kr South Korea KOREA UNIVERSTY COLLEGE OF MEDICINE (KUMC)Disease:
Acute lymphoblastic leukemia
-
KUMCi002-A (MM_CD34+iPSCs)
1 kr South Korea KOREA UNIVERSTY COLLEGE OF MEDICINE (KUMC)Disease:
Multiple myeloma
-
LCPHi001-A
1 cn China The Institute for Tissue Engineering and Regenerative Medicine, Liaocheng People's Hospital (LCPH)Disease:
Obsolete_parkinson's disease
-
LCPHi003-A
1 cn China The Institute for Tissue Engineering and Regenerative Medicine, Liaocheng People's Hospital (LCPH)Disease:
Parkinson disease
-
LUMCi029-A (LUMC0072iCTRL01)
1 nl Netherlands Leiden University Medical Center (LUMC)Disease:
Normal (average)
-
LUMCi029-B (LUMC0004iCTRL10)
1 nl Netherlands Leiden University Medical Center (LUMC)Disease:
Normal (average)
-
LUMCi039-A (LQT1-1781G/A hiPSC and LUMC0021iKCNQ-30)
1 nl Netherlands Leiden University Medical Center (LUMC)Disease:
Long qt syndrome 1
-
LUMCi054-A (CRB1 patient c.3122T>C p.(Met1041Thr) homozygote and LUMC0116iCRB09)
1 nl Netherlands Leiden University Medical Center (LUMC)Disease:
Retinitis pigmentosa
-
LUMCi054-A-1 (LUMC0116iCRB09 ISO-02, LUMC0116iCRB09 homozygote CRISPR corrected isogenic clone 02 and iso02LUMC0116iCRB09)
1 nl Netherlands Leiden University Medical Center (LUMC)Disease:
Retinitis pigmentosa
-
LUMCi054-A-2 (LUMC0116iCRB09 ISO-03, LUMC0116iCRB09 heterozygote CRISPR corrected isogenic clone 03 and iso03LUMC0116iCRB09)
1 nl Netherlands Leiden University Medical Center (LUMC)Disease:
Retinitis pigmentosa
-
LUMCi055-A (CRB1 patient 117 compound heterozygous 2983G>T p.(Glu995*) c.1892A>G, p.(Tyr631Cys) and LUMC0117iCRB01)
1 nl Netherlands Leiden University Medical Center (LUMC)Disease:
Retinitis pigmentosa
-
LUMCi056-A (CRB1 patient 128 compound heterozygous c.2843G>A p.(Cys948Tyr) and c.3122T>C p.(Met1041Thr) and LUMC0128iCRB01)
1 nl Netherlands Leiden University Medical Center (LUMC)Disease:
Retinitis pigmentosa
-
LUMCi056-A-1 (LUMC0128iCRB01 heterozygote CRISPR corrected isogenic clone 02 and iso02LUMC0128iCRB01)
1 nl Netherlands Leiden University Medical Center (LUMC)Disease:
Retinitis pigmentosa
-
MCRIi001-A-1 (PB001-OI26)
1 au Australia Murdoch Children's Research Institute (MCRI)Disease:
Osteogenesis imperfecta
-
MDCi008-A (8993-B12)
1 de Germany Max Delbrück Center Berlin Buch (MDC)Disease:
Leigh disease
-
MDCi009-A (8993-C11)
1 de Germany Max Delbrück Center Berlin Buch (MDC)Disease:
Leigh disease
-
MILi001-A (K10 and hFF-iPSCs)
1 de Germany Miltenyi Biotec B.V. & Co. KG (MIL)Disease:
Normal (average)
-
MILi001-B (F5)
1 de Germany Miltenyi Biotec B.V. & Co. KG (MIL)Disease:
Normal (average)
-
MILi001-C (F10)
1 de Germany Miltenyi Biotec B.V. & Co. KG (MIL)Disease:
Normal (average)
-
MLUi001-M
1 de Germany Medical Faculty of the Martin Luther University Halle-Wittenberg (MLU)Disease:
Schizophrenia
-
MLUi002-G
1 de Germany Medical Faculty of the Martin Luther University Halle-Wittenberg (MLU)Disease:
Schizophrenia
-
MMCi001-A (MMC-iPSC-052B-02)
1 tw Taiwan Mackay Medical College (MMC)Disease:
Deafness, autosomal recessive 1a
-
MNZTASi034-A (MS_0034.1)
1 au Australia Menzies Institute for Medical Research (MNZTAS)Disease:
Normal (average)
-
MPIi002-A (T4 and L1-1Mut)
1 de Germany Max Planck Institute for Molecular Biomedicine (MPI)Disease:
Obsolete_parkinson's disease
-
MRIi018-A (HLHS_375)
1 de Germany Klinikum rechts der Isar (MRI)Disease:
Hypoplastic left heart syndrome
-
MRIi024-A (Shox2.2)
1 de Germany Klinikum rechts der Isar (MRI)Disease:
Atrial fibrillation
-
MSKi002-A (C27 and iPS-27)
1 us United States Memorial Sloan Kettering Cancer Center (MSK)Disease:
Normal (average)
-
WAe009-A-1J (H9::mcherry cyto-reporter line)
2 us United States Memorial Sloan Kettering Cancer Center (MSK)Disease:
Normal (average)
-
WAe009-A-1W (H9 EF1A-mCherry-noPuro 803_AAVS-iSHH #3)
2 us United States Memorial Sloan Kettering Cancer Center (MSK)Disease:
Normal (average)
-
MUi010-A (MYH9)
1 th Thailand Mahidol University (MU)Disease:
Myh9-related disease
-
MUi015-A (RB1)
1 th Thailand Mahidol University (MU)Disease:
Retinoblastoma
-
MUBi002-A (CF 001)
1 pl Poland Medical University of Bialystok (MUB)Disease:
Cystic fibrosis
-
MURAi003-A (HoHLA, Homozygous-HLA and HoHLA C3)
1 th Thailand Faculty of Medicine Ramathibodi Hospital (MURA)Disease:
Normal (average)
-
MUSIi001-A-2 (HLA-I/II-null SFiPSCs)
1 th Thailand Faculty of Medicine Siriraj Hospital (MUSI)Disease:
Normal (average)
-
MUSIi016-A (TyO)
1 th Thailand Faculty of Medicine Siriraj Hospital (MUSI)Disease:
Normal (average)
-
NCHi003-A (NCH005)
1 us United States Nationwide Children's Hospital (NCH)Disease:
Pulmonary valve atresia with intact ventricular septum
-
NCHi006-A (NCH023)
1 us United States Nationwide Children's Hospital (NCH) UNKNOWN -
NCHi013-A (NCH17)
1 us United States Nationwide Children's Hospital (NCH)Disease:
Pulmonary valve atresia with intact ventricular septum
-
NCHi014-A (NCH3-N1HET)
1 us United States Nationwide Children's Hospital (NCH)Disease:
Normal (average)
-
NCHi015-A (NCH178)
1 us United States Nationwide Children's Hospital (NCH)Disease:
Type i truncus arteriosus
-
NCHi023-A (NCH217)
1 us United States Nationwide Children's Hospital (NCH)Disease:
Nemaline myopathy
-
WAe001-A-65
2 cn China Nanfang Hospital, Southern Medical University (NFYY)Disease:
Epileptic encephalopathy
-
NIHTVBi028-A
1 us United States National Institutes of Health-National Heart, Lung, and Blood Institute (NIHTVB)Disease:
Lyn gene mutation
-
NIHTVBi029-A (HT1127A (NIHTVBi029-A))
1 us United States National Institutes of Health-National Heart, Lung, and Blood Institute (NIHTVB)Disease:
Cdc42
-
NIHTVBi030-A (HT1128A (NIHTVBi030-A))
1 us United States National Institutes of Health-National Heart, Lung, and Blood Institute (NIHTVB)Disease:
Cdc42 gene
-
NIHTVBi031-A (HT1129D)
1 us United States National Institutes of Health-National Heart, Lung, and Blood Institute (NIHTVB)Disease:
Autoimmune interstitial lung, joint, and kidney disease
-
TMOi001-A-5 (DISC1 Ex2 D5)
1 de Germany NMI Natural and Medical Sciences Institute at the University of Tübingen (NMI)Disease:
Normal (average)
-
NMIi010-A
1 de Germany NMI Natural and Medical Sciences Institute at the University of Tübingen (NMI)Disease:
Normal (average)
-
NMIi011-A (B1.4)
1 de Germany NMI Natural and Medical Sciences Institute at the University of Tübingen (NMI)Disease:
Breast carcinoma
-
NMIi011-B (B1.6)
1 de Germany NMI Natural and Medical Sciences Institute at the University of Tübingen (NMI)Disease:
Breast carcinoma
-
NMIi011-C (B1.7)
1 de Germany NMI Natural and Medical Sciences Institute at the University of Tübingen (NMI)Disease:
Breast carcinoma
-
NMIi011-D (B1.10)
1 de Germany NMI Natural and Medical Sciences Institute at the University of Tübingen (NMI)Disease:
Breast carcinoma
-
NSi003-A (NSi-DS)
1 in India Stem Cell and Neurobiology Lab (NS)Disease:
Down syndrome
-
NSi003-B (NSi-isoEu)
1 in India Stem Cell and Neurobiology Lab (NS)Disease:
Down syndrome
-
NTUHi002-A
1 tw Taiwan National Taiwan University Hospital (NTUH)Disease:
Aceruloplasminemia
-
NTUHi004-A
1 tw Taiwan National Taiwan University Hospital (NTUH)Disease:
Leigh syndrome
-
NTUHi005-A (IBMS-iPSC-071-01)
1 tw Taiwan National Taiwan University Hospital (NTUH) UNKNOWN -
NUIGi001-A (iPSC ARO1-11)
1 ie Ireland National University of Ireland Galway (NUIG)Disease:
Autosomal recessive osteopetrosis
-
OTATi001-A (HC4)
1 us United States Office of Tissues and Advanced Therapies, CBER, FDA (OTAT)Disease:
Normal (average)
-
PCIi029-A (PC076)
1 fr France PHENOCELL (PCI)Disease:
Waardenburg syndrome type 1
-
PCIi030-A (PC078)
1 fr France PHENOCELL (PCI)Disease:
Waardenburg syndrome type 1
-
PCIi031-A (PC079)
1 fr France PHENOCELL (PCI)Disease:
Waardenburg syndrome type 1
-
PEIi021-A (PEIi004-A)
1 de Germany Paul-Ehrlich-Institut (PEI)Disease:
Leukocyte adhesion deficiency type 1
-
PEIi022-A (PEIi005-A)
1 de Germany Paul-Ehrlich-Institut (PEI)Disease:
Leukocyte adhesion deficiency type 1
-
PFIZi001-A (EM1-3F)
1 gb United Kingdom Pfizer Limited - Pfizer (PFIZ)Disease:
Primary erythromelalgia
-
RCi001-A (Thp3C-6 and RCi88)
1 gb United Kingdom Pfizer Limited - Pfizer (PFIZ)Disease:
Primary erythromelalgia
-
RCi001-B (RCi89 and Thp3C-9)
1 gb United Kingdom Pfizer Limited - Pfizer (PFIZ)Disease:
Primary erythromelalgia
-
RCi002-A (FP5C-14 and RCi92)
1 gb United Kingdom Pfizer Limited - Pfizer (PFIZ)Disease:
Primary erythromelalgia
-
RCi002-B (FP5C-16 and RCi93)
1 gb United Kingdom Pfizer Limited - Pfizer (PFIZ)Disease:
Primary erythromelalgia
-
RCi003-A (RCi115 and CIP11A-5)
1 gb United Kingdom Pfizer Limited - Pfizer (PFIZ)Disease:
Pain agnosia
-
RCi003-B (CIP11A-9 and RCi117)
1 gb United Kingdom Pfizer Limited - Pfizer (PFIZ)Disease:
Pain agnosia
-
PNUSCRi001-A (GBA PD iPSC7)
1 kr South Korea Pusan National University: Convergence Stem Cell Research Center (PNUSCR)Disease:
Parkinson disease
-
PNUSCRi002-A (GBA PD iPSC9)
1 kr South Korea Pusan National University: Convergence Stem Cell Research Center (PNUSCR)Disease:
Parkinson disease
-
PNUSCRi003-A (GBA Gaucher iPSC1)
1 kr South Korea Pusan National University: Convergence Stem Cell Research Center (PNUSCR)Disease:
Gaucher disease
-
PNUSCRi004-A (GBA PD iPSC8)
1 kr South Korea Pusan National University: Convergence Stem Cell Research Center (PNUSCR)Disease:
Parkinson disease
-
PNUSCRi005-A
1 kr South Korea Pusan National University: Convergence Stem Cell Research Center (PNUSCR)Disease:
Hunter syndrome
-
WAe009-A-47
2 cn China Peking University Third Hospital Department of Cardiology (PUHT)Disease:
Cytochrome-c oxidase deficiency disease
-
PUMCHi020-A
1 cn China Peking Union Medical College Hospital (PUMCH)Disease:
Aicardi-goutieres syndrome
-
RCi004-A (PDSC-10 and RCi150)
1 gb United Kingdom Roslin Cells (RC)Disease:
Huntington disease
-
RCe020-A (RC-16 and RC16)
2 gb United Kingdom Roslin Cells (RC)Disease:
Normal (average)
-
RCMGi001-A (P1L5)
1 ru Russia Research Centre for Medical Genetics (RCMG)Disease:
Cystic fibrosis
-
RCMGi002-A (P7L2)
1 ru Russia Research Centre for Medical Genetics (RCMG)Disease:
Cystic fibrosis
-
RCMGi004-A (P6L2)
1 ru Russia Research Centre for Medical Genetics (RCMG)Disease:
Cystic fibrosis
-
RCMGi004-B (P6L8)
1 ru Russia Research Centre for Medical Genetics (RCMG)Disease:
Cystic fibrosis
-
RCMGi005-A (P5L1)
1 ru Russia Research Centre for Medical Genetics (RCMG)Disease:
Cystic fibrosis
-
RCMGi005-B (P5L5)
1 ru Russia Research Centre for Medical Genetics (RCMG)Disease:
Cystic fibrosis
-
RCMGi011-A (P10L1)
1 ru Russia Research Centre for Medical Genetics (RCMG)Disease:
Mucopolysaccharidosis type ivb
Disease:
Autosomal recessive nonsyndromic deafness 12
-
RCMGi015-A (P16L4)
1 ru Russia Research Centre for Medical Genetics (RCMG)Disease:
Glycogen storage disease i
-
RCMGi016-A (P17L16)
1 ru Russia Research Centre for Medical Genetics (RCMG)Disease:
Glycogen storage disease i
-
RCPCMi003-A (ATXN1KCl2)
1 ru 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
-
RCPCMi004-A (Park14-4)
1 ru 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
-
RCPCMi005-A (IPSP12-1)
1 ru 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
-
RCPCMi007-A (IPSFF1S)
1 ru Russia Federal State Budgetary Institution Federal Research and Clinical Center of Physical-Chemical Medicine of Federal Medical Biological Agency (RCPCM)Disease:
Normal (average)
-
RCPCMi008-A (IPS SCA17 sev cln4)
1 ru 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
-
RCPCMi009-A (IPSRG4S and UEF-3B)
1 fi Finland Federal State Budgetary Institution Federal Research and Clinical Center of Physical-Chemical Medicine of Federal Medical Biological Agency (RCPCM)Disease:
Normal (average)
-
RCPCMi010-A (iPS 67-7)
1 ru 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
-
RCSIi001-A (iPDK)
1 ie Ireland Royal College of Surgeons in Ireland (RCSI)Disease:
Normal (average)
-
REGUi001-A (IPS4FLV)
1 fr France Institute for Regenerative Medecine & Biotherapy U1183 (REGU)Disease:
Normal (average)
-
REGUi009-A (myasthenic syndrome due to mutation in ColQ and hiPS 5-9016)
1 fr France Institute for Regenerative Medecine & Biotherapy U1183 (REGU)Disease:
Congenital myasthenic syndrome
-
RGIe049-A (SI-137)
2 us United States Reproductive Genetics Institute (RGI)Disease:
Neurofibromatosis
-
RGIe050-A (SI-138)
2 us United States Reproductive Genetics Institute (RGI)Disease:
Neurofibromatosis
-
RGIe051-A (SI-139)
2 us United States Reproductive Genetics Institute (RGI)Disease:
Neurofibromatosis
-
RGIe052-A (SI-140)
2 us United States Reproductive Genetics Institute (RGI)Disease:
Neurofibromatosis
-
RGIe053-A (SI-141)
2 us United States Reproductive Genetics Institute (RGI)Disease:
Neurofibromatosis type 1
-
RGIe134-A (SI-235)
2 us United States Reproductive Genetics Institute (RGI)Disease:
Neurofibromatosis
-
RIi005-A (TYR.1.H.iPSC.1)
1 ir Iran Royan Institute (RI)Disease:
Tyrosinemia type 1
-
KUIFMSi004-A-1 (hPSC MPP8 Neon Green)
1 ru Russia Pirogov Russian National Research Medical University (RNRMU)Disease:
Normal (average)
-
RUESe001-A (RUES1)
2 us United States The Rockefeller University (RUES)Disease:
Normal (average)
-
RUESe002-A-6 (RUES2-GLR)
2 us United States The Rockefeller University (RUES)Disease:
Normal (average)
-
SAPi002-A (ALS I, ALS I–FUS-R514S/wt and FUS-R514S/wt)
1 it Italy Sapienza University of Rome (SAP)Disease:
Amyotrophic lateral sclerosis
-
SAPi003-A (ALS II, FUS-R521C/wt and ALS II–FUS-R521C/wt)
1 it Italy Sapienza University of Rome (SAP)Disease:
Amyotrophic lateral sclerosis
-
SAPi004-A (ALS III, TDP43-A382T/A382T and ALS III-TDP43-A382T/A382T)
1 it Italy Sapienza University of Rome (SAP)Disease:
Amyotrophic lateral sclerosis
-
SBWCHi001-A
1 cn China Shenzhen Baoan Women's and Children's Hospital, Jinan University (SBWCH)Disease:
Ctnnb1 gene mutation
-
SCAUi001-A
1 cn China South China Agricultural University (SCAU)Disease:
Normal (average)
-
SCHi001-A-1 (AMN5-Corrected iPSC)
1 kr South Korea Severance Children’s Hospital (SCH)Disease:
Adrenoleukodystrophy
-
SCVIi051-A (477)
1 us United States Stanford Cardiovascular Institute (SCVI)Disease:
Normal (average)
-
SCVIi053-A (2021)
1 us United States Stanford Cardiovascular Institute (SCVI)Disease:
Normal (average)
-
SCVIi073-A (SCVIi574C2)
1 us United States Stanford Cardiovascular Institute (SCVI)Disease:
Dilated cardiomyopathy
-
SCVIi128-A (SCVI766)
1 us United States Stanford Cardiovascular Institute (SCVI)Disease:
Marfan syndrome
-
SCVIi129-A (SCVI2454)
1 us United States Stanford Cardiovascular Institute (SCVI)Disease:
Marfan syndrome
-
SDQLCHi061-A
1 cn China Children’s Hospital affiliated to Shandong University (SDQLCH)Disease:
Carbamoyl phosphate synthetase i deficiency disease
-
SDQLCHi067-A
1 cn China Children’s Hospital affiliated to Shandong University (SDQLCH)Disease:
Subcortical band heterotopia
-
SDQLCHi068-A
1 cn China Children’s Hospital affiliated to Shandong University (SDQLCH)Disease:
Immunodeficiency 14a, autosomal dominant
-
SDUe001-A (Odense3)
2 dk Denmark University of Southern Denmark (SDU) UNKNOWN -
SHEHi002-A (iPS36)
1 cn China Shanghai East Hospital (SHEH)Disease:
Long qt syndrome 8
-
SMBCi011-A
1 cn China Shandong Medicinal Biotechnology Center (SMBC)Disease:
Prader-willi syndrome
-
SMUSHi002-A
1 cn China Southern Medical University Shenzhen hospital (SMUSH)Disease:
Normal (average)
-
SNUe007-A (SNUhES31)
2 kr South Korea Seoul National University (SNU)Disease:
Normal (average)
-
UOSe012-A-1
2 gb United Kingdom University of Southampton (SOTON)Disease:
Normal (average)
-
SPHi001-A (SLEi002HZY)
1 cn China Shenzhen People's Hospital (SPH)Disease:
Systemic lupus erythematosus
-
WAe009-A-48
2 cn China Shenzhen People's Hospital (SPH)Disease:
Long qt syndrome 3
-
WAe009-A-74
2 cn China Shenzhen People's Hospital (SPH)Disease:
Long qt syndrome 2
-
WAe009-A-88
2 cn China Shenzhen People's Hospital (SPH)Disease:
Long qt syndrome 2
-
SPPHIi003-A
1 cn China Sichuan Academy of Medical Science & Sichuan Provincial People’s Hospital (SPPHI) UNKNOWN -
SUSMi005-A
1 us United States Stanford University School of Medicine (SUSM)Disease:
Obsolete_parkinson's disease
-
WAe001-A-81
2 cn China The Seventh Affiliated Hospital (SYSUSH)Disease:
Normal (average)
-
SZBKi003-A
1 cn China Shenzhen Beike Biotechnology Co., Ltd. (SZBK)Disease:
Normal (average)
-
SZGJMSi001-A (ZLP-2)
1 cn China Research Center of Biological Psychiatry, Suzhou Guangji hospital (SZGJMS)Disease:
Schizophrenia
-
SZGJMSi002-A (TSQ-1)
1 cn China Research Center of Biological Psychiatry, Suzhou Guangji hospital (SZGJMS)Disease:
Obsessive-compulsive disorder
-
SZGJMSi003-A (TSH-2)
1 cn China Research Center of Biological Psychiatry, Suzhou Guangji hospital (SZGJMS)Disease:
Normal (average)
-
SZGJMSi004-A (WJM-1)
1 cn China Research Center of Biological Psychiatry, Suzhou Guangji hospital (SZGJMS)Disease:
Depression
-
TCIERi001-A (IER-EK1)
1 tw Taiwan Institute of Eye Research, Hualien Tzu Chi Hospital (TCIER)Disease:
Normal (average)
-
TMPi014-A (MR030 c1 and MR-030 c1)
1 ch Switzerland Translational Molecular Psychiatry (TMP)Disease:
Attention deficit hyperactivity disorder
-
TNRMCi001-A (iTAF32)
1 ru Russia Tomsk National Research Medical Center of the Russian Academy of Sciences (TNRMC)Disease:
Cystic fibrosis
-
TRNDi042-A (HT528A)
1 us United States NIH/NCATS-TRND Branch (TRND)Disease:
Mucopolysaccharidosis type iiib
-
TUSMi001-A
1 cn China Tongji University School of Medicine (TUSM)Disease:
Normal (average)
-
TUSMi002-A
1 cn China Tongji University School of Medicine (TUSM)Disease:
Normal (average)
-
TUSMi003-A
1 cn China Tongji University School of Medicine (TUSM)Disease:
Alzheimer's disease
-
TUSMi004-A
1 cn China Tongji University School of Medicine (TUSM)Disease:
Obsessive-compulsive disorder
-
TUSMi005-A
1 cn China Tongji University School of Medicine (TUSM)Disease:
Obsolete_bipolar disorder
-
UCLi005-A (LGMD2D Pt. 4 and LGMD2D #4)
1 gb United Kingdom University College London (UCL)Disease:
Limb-girdle muscular dystrophy
-
UCLi024-A (SMID277 and GOS111B)
1 gb United Kingdom University College London (UCL)Disease:
Argininosuccinic aciduria
-
WAe001-A-10 (H1_RB1ex3_G3)
2 de Germany Universität Duisburg-Essen (UDE)Disease:
Retinoblastoma
-
UGOTSAi002-B (N1-001iC2)
1 se Sweden The Sahlgrenska Academy at University of Gothenburg (UGOTSA)Disease:
Alzheimer's disease
-
UGOTSAi003-A (N1-002iC3A)
1 se Sweden The Sahlgrenska Academy at University of Gothenburg (UGOTSA)Disease:
Alzheimer's disease
-
UGOTSAi003-B (N1-002iC4)
1 se Sweden The Sahlgrenska Academy at University of Gothenburg (UGOTSA)Disease:
Alzheimer's disease
-
UGOTSAi004-A (N1-003iC3)
1 se Sweden The Sahlgrenska Academy at University of Gothenburg (UGOTSA)Disease:
Alzheimer's disease
-
UGOTSAi004-B (N1-003iC4)
1 se Sweden The Sahlgrenska Academy at University of Gothenburg (UGOTSA)Disease:
Alzheimer's disease
-
UGOTSAi005-A (N1-004iC2)
1 se Sweden The Sahlgrenska Academy at University of Gothenburg (UGOTSA)Disease:
Normal (average)
-
UGOTSAi005-B (N1-004iC6)
1 se Sweden The Sahlgrenska Academy at University of Gothenburg (UGOTSA)Disease:
Normal (average)
-
UGOTSAi006-A (N1-005iC1)
1 se Sweden The Sahlgrenska Academy at University of Gothenburg (UGOTSA)Disease:
Alzheimer's disease
-
UHi006-A-3 (HEL24.3_IFIH1KO)
1 fi Finland University of Helsinki (UH)Disease:
Type i diabetes mellitus
-
UIOi001-A (AG27)
1 no Norway University of Oslo (UIO)Disease:
Normal (average)
-
UIOi006-A (iPSC APOE4/4: Sporadic AD (Coriell #AG10788, female, Age 87))
1 no Norway University of Oslo (UIO) UNKNOWN -
UJSi001-A
1 cn China Jiangsu University (UJS)Disease:
Schizophrenia
-
UKAi010-A (BM 104-12)
1 de Germany Universitätsklinikum Aachen (UKA)Disease:
Normal (average)
-
UKEi001-A (ERC001sv1162)
1 de Germany University Medical Center Hamburg-Eppendorf (UKE)Disease:
Normal (average)
-
UKEi001-A-1 (CRYABhom)
1 de Germany University Medical Center Hamburg-Eppendorf (UKE)Disease:
Desminopathy
-
UKEi001-B (ERC001sv1352)
1 de Germany University Medical Center Hamburg-Eppendorf (UKE)Disease:
Normal (average)
-
UKEi001-C (ERC001sv1355)
1 de Germany University Medical Center Hamburg-Eppendorf (UKE)Disease:
Normal (average)
-
UKEi002-A (ERC017sv2575)
1 de Germany University Medical Center Hamburg-Eppendorf (UKE)Disease:
Normal (average)
-
UKEi002-C (ERC017sv2596)
1 de Germany University Medical Center Hamburg-Eppendorf (UKE)Disease:
Normal (average)
-
UKEi003-A (ERC018sv1583)
1 de Germany University Medical Center Hamburg-Eppendorf (UKE)Disease:
Normal (average)
-
UKEi003-B (ERC018sv1590)
1 de Germany University Medical Center Hamburg-Eppendorf (UKE)Disease:
Normal (average)
-
UKEi003-C (ERC018sv1634)
1 de Germany University Medical Center Hamburg-Eppendorf (UKE)Disease:
Normal (average)
-
HVRDe006-A-1
2 us United States Universitätsklinikum Erlangen (UKER)Disease:
Coffin-siris syndrome
-
UKJi001-A (PKP2-hiPSC)
1 de Germany Universitätsklinikum Jena (UKJ), Klinik für Innere Medizin I (KIM I), Dr. M. Bekhite ELsaied (UKJ)Disease:
Normal (average)
-
UKJi003-A (hiPSC-FD)
1 de Germany Universitätsklinikum Jena (UKJ), Klinik für Innere Medizin I (KIM I), Dr. M. Bekhite ELsaied (UKJ)Disease:
Fabry disease
-
UKJi004-A (hiPSC-WT)
1 de Germany Universitätsklinikum Jena (UKJ), Klinik für Innere Medizin I (KIM I), Dr. M. Bekhite ELsaied (UKJ)Disease:
Normal (average)
-
UKJi006-A (PKP2-hiPSC-ARVC)
1 de Germany Universitätsklinikum Jena (UKJ), Klinik für Innere Medizin I (KIM I), Dr. M. Bekhite ELsaied (UKJ)Disease:
Arrhythmogenic right ventricular cardiomyopathy
-
UKKi035-B (NP0139-B and NP0139-6C)
1 de Germany Klinikum der Universität zu Köln (UKK)Disease:
Rare hypertrophic cardiomyopathy
-
UMILi024-A (CTL04)
1 it Italy University of Milan (UMIL)Disease:
Normal (average)
-
WAe009-A-37 (H9-GSX2-tTA:GFP)
2 it Italy University of Milan (UMIL)Disease:
Normal (average)
-
UNAMi002-A (IFC-UNAM iPD02-S)
1 mx Mexico Instituto de Fisiología Celular, Universidad Nacional Autónoma de México (UNAM)Disease:
Parkinson disease
-
UNAMi003-A (IFC-UNAM iPD03-PINK1)
1 mx Mexico Instituto de Fisiología Celular, Universidad Nacional Autónoma de México (UNAM)Disease:
Parkinson disease
-
UNIPDi004-A
1 it Italy University of Padova (UNIPD)Disease:
Normal (average)
-
UNIPDi004-B (HDP04)
1 it Italy University of Padova (UNIPD)Disease:
Normal (average)
-
UOSe001-A (MasterShef1, MShef1 and MstrShef1)
2 gb United Kingdom University of Sheffield (UOS)Disease:
Normal (average)
-
UOSe007-A (MstrShef2, MShef2 and MasterShef2)
2 gb United Kingdom University of Sheffield (UOS)Disease:
Normal (average)
-
UOSe008-A (MstrShef3, MShef3 and MasterShef3)
2 gb United Kingdom University of Sheffield (UOS)Disease:
Normal (average)
-
UOSe009-A (MstrShef4, MShef4 and MasterShef4)
2 gb United Kingdom University of Sheffield (UOS)Disease:
Normal (average)
-
UOSe010-A (MstrShef5, MShef5 and MasterShef5)
2 gb United Kingdom University of Sheffield (UOS)Disease:
Normal (average)
-
UOSe011-A (MstrShef6, MShef6 and MasterShef6)
2 gb United Kingdom University of Sheffield (UOS)Disease:
Normal (average)
-
UOSe012-A (MstrShef7, MShef7 and MasterShef7)
2 gb United Kingdom University of Sheffield (UOS)Disease:
Normal (average)
-
UOSe013-A (MstrShef8, MasterShef8 and MShef8)
2 gb United Kingdom University of Sheffield (UOS)Disease:
Normal (average)
-
UOSe014-A (MasterShef10, MShef10 and MstrShef10)
2 gb United Kingdom University of Sheffield (UOS)Disease:
Normal (average)
-
UOSe015-A (MasterShef11, MstrShef11 and MShef11)
2 gb United Kingdom University of Sheffield (UOS)Disease:
Normal (average)
-
UOSe016-A (MasterShef12, MShef12 and MstrShef12)
2 gb United Kingdom University of Sheffield (UOS)Disease:
Normal (average)
-
UOSe017-A (MasterShef13, MstrShef13 and MShef13)
2 gb United Kingdom University of Sheffield (UOS)Disease:
Normal (average)
-
UOSe018-A (MasterShef14, MShef14 and MstrShef14)
2 gb United Kingdom University of Sheffield (UOS)Disease:
Normal (average)
-
UTHSCHi001-A (NDC-AD01)
1 us United States The University of Texas Health Science Center at Houston (UTHSCH)Disease:
Alzheimer's disease
-
VIACe001-A-1 (BG01V/hOG)
2 us United States Novocell, Inc. (VIAC) UNKNOWN -
WAe001-A (WA01 and H1)
2 us United States WiCell Research Institute (WA)Disease:
Normal (average)
-
WAe007-A (H7 and WA07)
2 us United States WiCell Research Institute (WA)Disease:
Normal (average)
-
WAe009-A (WA09 and H9)
2 us United States WiCell Research Institute (WA)Disease:
Normal (average)
-
WAe013-A (WA13 and H13)
2 us United States WiCell Research Institute (WA) UNKNOWN -
WAe014-A (WA14 and H14)
2 us United States WiCell Research Institute (WA) UNKNOWN -
WIBRe001-A-2 (WIBR3 Oct4-2A-GFP)
2 us United States Whitehead Institute for Biomedical Research (WIBR)Disease:
Normal (average)
-
WIBRe004-A (WIN1 and Whitehead Institute Naive Human 1)
2 us United States Whitehead Institute for Biomedical Research (WIBR)Disease:
Normal (average)
-
WTSIi001-A (HPSI1213i-pahc_4)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi037-A (HPSI0114i-zoxy_3)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi038-A (HPSI1113i-ieki_3)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi046-B (HPSI0214i-wibj_1)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi047-B (HPSI0814i-bokz_6)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi049-A (HPSI0514i-wiii_2)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi049-B (HPSI0514i-wiii_3)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi052-A (HPSI1114i-ziyn_6)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi053-A (HPSI0413i-corn_1)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi054-B (HPSI0413i-nudd_6)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi056-A (HPSI0513i-dipe_1)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi057-B (HPSI0513i-giuf_1)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi059-A (HPSI0513i-uilw_1)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi063-A (HPSI0613i-aevs_1)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi068-B (HPSI0613i-giuo_4)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi069-A (HPSI0613i-hegp_3)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi073-A (HPSI0314i-sojd_3)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi082-A (HPSI1013i-cups_3)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi083-A (HPSI1213i-xuja_2)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi085-A (HPSI1113i-eofe_1)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi086-A (HPSI0913i-coyi_3)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi098-A (HPSI1213i-nekd_1)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi102-A (HPSI0413i-iakz_2)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi102-B (HPSI0413i-iakz_1)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi103-A (HPSI1213i-nusw_2)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi104-A (HPSI0513i-coio_2)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi104-B (HPSI0513i-coio_1)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi105-A (HPSI0313i-airc_2)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi105-B (HPSI0313i-airc_66)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi106-B (HPSI0613i-hikj_1)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi109-A (HPSI0413i-coxy_3)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi109-B (HPSI0413i-coxy_33)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi110-A (HPSI0713i-darw_1)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi111-A (HPSI0513i-euir_1)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi112-A (HPSI0613i-funp_3)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi114-A (HPSI0513i-golb_1)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi115-A (HPSI0513i-iasn_3)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi116-A (HPSI0813i-iicq_1)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi117-A (HPSI0613i-liun_2)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi118-A (HPSI0813i-meqo_2)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi119-A (HPSI0613i-oefg_2)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi120-A (HPSI0513i-oeoo_2)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi121-A (HPSI0413i-ougl_1)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi121-B (HPSI0413i-ougl_3)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi122-A (HPSI0413i-peop_2)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi123-A (HPSI0713i-qimz_1)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi124-A (HPSI0713i-ruyv_1)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi124-B (HPSI0713i-ruyv_3)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi125-A (HPSI0413i-uahf_3)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi126-A (HPSI0913i-vopm_2)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi127-A (HPSI0413i-xekf_1)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi128-A (HPSI0413i-yuze_1)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi129-A (HPSI0613i-zisa_3)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi130-A (HPSI0713i-aehn_22)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi131-A (HPSI0513i-aipt_33)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi133-A (HPSI0713i-dard_1)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi133-B (HPSI0713i-dard_2)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi134-B (HPSI0513i-dulv_2)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi137-A (HPSI0613i-lizq_1)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi137-B (HPSI0613i-lizq_3)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi138-A (HPSI0414i-mita_2)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi139-A (HPSI1113i-oaaz_2)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi140-A (HPSI0613i-oomz_22)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi141-A (HPSI0613i-qanu_1)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi142-A (HPSI0613i-qony_1)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi144-A (HPSI0114i-wegi_1)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi145-A (HPSI0813i-wots_3)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi146-A (HPSI0613i-xosg_2)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi168-A (HPSI0214i-poih_4)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi168-B (HPSI0214i-poih_2)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi169-A (HPSI0614i-miaj_6)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi170-B (HPSI1213i-tolg_6)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi171-A (HPSI0914i-zerv_7)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi171-B (HPSI0914i-zerv_8)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi172-A (HPSI0914i-laey_6)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi172-B (HPSI0914i-laey_4)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi173-A (HPSI0414i-naju_1)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi174-A (HPSI0614i-paab_4)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi175-A (HPSI1014i-tixi_4)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi176-B (HPSI0714i-iudw_4)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi177-A (HPSI0414i-xojn_3)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi178-B (HPSI0215i-fawm_4)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi179-A (HPSI0314i-wigw_2)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi180-A (HPSI0514i-puie_4)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi180-B (HPSI0514i-puie_5)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi181-A (HPSI0514i-rutc_2)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi182-A (HPSI0614i-kegd_2)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi183-A (HPSI0414i-oaqd_2)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi183-B (HPSI0414i-oaqd_3)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi184-A (HPSI1014i-qayj_3)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi184-B (HPSI1014i-qayj_4)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi186-A (HPSI1014i-babz_3)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi187-A (HPSI1013i-sita_1)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi188-A (HPSI1014i-kefb_1)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi189-A (HPSI1014i-quls_2)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi190-A (HPSI0914i-kajh_3)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
WTSIi191-A (HPSI0215i-oilg_3)
1 gb United Kingdom Wellcome Sanger Institute (WTSI)Disease:
Normal (average)
-
XACHi004-A
1 cn China Xi'an children's hospital (XACH)Disease:
Atrial fibrillation
-
XXMUFAi001-A
1 cn China The First Affiliated Hospital of Xinxiang Medical University (XXMUFA)Disease:
Long qt syndrome 2
-
YBLi004-A (YBL/SH/2018/0062)
1 in India Yashraj Biotechnology ltd Navi Mumbai India (YBL)Disease:
Normal (average)
-
YBLi005-A (YBL/OS/2021/00196)
1 in India Yashraj Biotechnology ltd Navi Mumbai India (YBL)Disease:
Normal (average)
-
YBLi006-A (YBL/PH/2022/0025)
1 in India Yashraj Biotechnology ltd Navi Mumbai India (YBL) UNKNOWN -
YUCMi020-A
1 kr South Korea Yonsei University College of Medicine (YUCM)Disease:
Normal (average)
-
ZJSHi001-A (ZJSHi-KCNB1)
1 cn China Department of Pediatrics, The Second Affiliated Hospital of Zhejiang University School of Medicine (ZJSH)Disease:
Developmental and epileptic encephalopathy, 26
-
WAe009-A-B
2 cn China Zhengzhou Central Hospital Affiliated (ZZCH)Disease:
Heart failure
-
ZZUNEUi010-A (CMF001-A)
1 cn China ZhengZhou University- The first affiliated hospital(ZZU) (ZZUNEU)Disease:
Juvenile amyotrophic lateral sclerosis
-
ZZUNEUi026-A
1 cn China ZhengZhou University- The first affiliated hospital(ZZU) (ZZUNEU)Disease:
Hypertrophic cardiomyopathy
-
WAe009-A-C
2 cn China The Second Affiliated Hospital (ZZUSA)Disease:
Heart failure