TAUi001-A-1

JPH2

General

Cell Line

hPSCreg name TAUi001-A-1
Cite as:
TAUi001-A-1 (RRID:CVCL_ZA78)
Alternative name(s)
JPH2
Cell line type Human induced pluripotent stem cell (hiPSC)
Similar lines
TAUi001-A
(UTA.09703.HCMJp)
Donor's gene variants:
JPH2
Donor diseases:
hypertrophic cardiomyopathy
ICANi001-A-1
(CDGEN1.16.40.5)
Donor diseases:
hypertrophic cardiomyopathy
UKEi070-A-1
(Rep 28, Iso Co)
Donor diseases:
hypertrophic cardiomyopathy
UKEi070-A-2
(Bi-allelic mutant, Mut 103)
Donor diseases:
hypertrophic cardiomyopathy
CIRMi893-A
(CW30205)
Donor diseases:
Hypertrophic Cardiomyopathy
SCVIi036-A
(SCVI248)
Donor diseases:
hypertrophic cardiomyopathy
SCVIi037-A
(SCVI672)
Donor diseases:
hypertrophic cardiomyopathy
CIRMi909-A
(CW30224)
Donor diseases:
Hypertrophic Cardiomyopathy
CIRMi919-A
(CW30234)
Donor diseases:
Hypertrophic Cardiomyopathy
ZJUi011-A
(ZJULLi003-A, LSYMYH7iPS)
Donor diseases:
Hypertrophic cardiomyopathy
CIRMi920-A
(CW30235)
Donor diseases:
Hypertrophic Cardiomyopathy
ZJUi012-A
(ZJULLi004-A, ZYLMYBPC3iPS)
Donor diseases:
Hypertrophic cardiomyopathy
WTSIi609-A
(HPSI0516i-suqd_3)
Donor diseases:
Rare hypertrophic cardiomyopathy
CIRMi937-A
(CW30256)
Donor diseases:
Hypertrophic Cardiomyopathy
UKKi035-A
(NP0139-A, NP0139-3E)
Donor's gene variants:
MYBPC3, MYBPC3
Donor diseases:
Rare hypertrophic cardiomyopathy
CIRMi947-A
(CW30266)
Donor diseases:
Hypertrophic Cardiomyopathy
UKKi035-B
(NP0139-B, NP0139-6C)
Donor's gene variants:
MYBPC3, MYBPC3
Donor diseases:
Rare hypertrophic cardiomyopathy
UKKi035-C
(NP0139-C, NP0139-24D)
Donor's gene variants:
MYBPC3, MYBPC3
Donor diseases:
Rare hypertrophic cardiomyopathy
WTSIi679-B
(HPSI0316i-ponl_4)
Donor diseases:
Rare hypertrophic cardiomyopathy
WTSIi685-B
(HPSI0416i-ioys_6)
Donor diseases:
Rare hypertrophic cardiomyopathy
WTSIi493-B
(HPSI0416i-ruah_5)
Donor diseases:
Rare hypertrophic cardiomyopathy
WTSIi508-B
(HPSI0416i-jewl_6)
Donor diseases:
Rare hypertrophic cardiomyopathy
WTSIi466-B
(HPSI0416i-aicq_4)
Donor diseases:
Rare hypertrophic cardiomyopathy
WTSIi483-B
(HPSI0416i-ourj_2)
Donor diseases:
Rare hypertrophic cardiomyopathy
CIRMi969-A
(CW30292)
Donor diseases:
Hypertrophic Cardiomyopathy
CIRMi970-A
(CW30293)
Donor diseases:
Hypertrophic Cardiomyopathy
CIRMi971-A
(CW30295)
Donor diseases:
Hypertrophic Cardiomyopathy
WTSIi460-B
(HPSI0516i-jepf_3)
Donor diseases:
Rare hypertrophic cardiomyopathy
WTSIi609-B
(HPSI0516i-suqd_6)
Donor diseases:
Rare hypertrophic cardiomyopathy
IBBISTi005-A
(F81 (940) clone 5)
Donor diseases:
Hypertrophic Cardiomyopathy
IBBISTi005-B
(F81 (940) clone 8)
Donor diseases:
Hypertrophic Cardiomyopathy
CIRMi982-A
(CW30310)
Donor diseases:
Hypertrophic Cardiomyopathy
CIRMi983-A
(CW30311)
Donor diseases:
Hypertrophic Cardiomyopathy
CIRMi984-A
(CW30312)
Donor diseases:
Hypertrophic Cardiomyopathy
CIRMi985-A
(CW30314)
Donor diseases:
Hypertrophic Cardiomyopathy
SCVIi096-A
(SCVI-675fs1)
Donor diseases:
Hypertrophic Cardiomyopathy
SCVIi097-A
(SCVI-675fs2)
Donor diseases:
Hypertrophic Cardiomyopathy
SCVIi098-A
(SCVI-675fs3)
Donor diseases:
Hypertrophic Cardiomyopathy
SCVIi099-A
(SCVI-675fs4)
Donor diseases:
Hypertrophic Cardiomyopathy
CIRMi999-A
(CW30329)
Donor diseases:
Hypertrophic Cardiomyopathy
CIRMi00A-A
(CW30331)
Donor diseases:
Hypertrophic Cardiomyopathy
WTSIi679-A
(HPSI0316i-ponl_2)
Donor diseases:
Rare hypertrophic cardiomyopathy
CIRMi746-A
(CW30024)
Donor diseases:
Hypertrophic Cardiomyopathy
WTSIi484-B
(HPSI0716i-bakv_4)
Donor diseases:
Rare hypertrophic cardiomyopathy
WTSIi685-A
(HPSI0416i-ioys_5)
Donor diseases:
Rare hypertrophic cardiomyopathy
CIRMi00J-A
(CW30340)
Donor diseases:
Hypertrophic Cardiomyopathy
WTSIi689-A
(HPSI0616i-newl_6)
Donor diseases:
Rare hypertrophic cardiomyopathy
Last update 21st June 2021
User feedback
No feedback available yet.

Login to share your feedback, experiences or results with the research community.

Provider

Generator Tampere University (TAU)
Derivation country Finland

External Databases

BioSamples SAMEA6880675
Cellosaurus CVCL_ZA78
Wikidata Q98133171

General Information

* Is the cell line readily obtainable for third parties?
Yes
Cell line can only be used in: Fit4purpose-OOC project
Research use: allowed
Clinical use: not allowed
Commercial use: allowed
Subclone of

Donor Information

General Donor Information

Sex male
Ethnicity Caucasian

Phenotype and Disease related information (Donor)

Diseases A disease was diagnosed.
The donor is a carrier of a disease-associated mutation and affected.
Synonyms
  • Asymmetric Septal Hypertrophies
  • Hypertrophic Obstructive Cardiomyopathies
  • Cardiomyopathy, hypertrophic
  • Subvalvular Stenosis, Idiopathic Hypertrophic
  • Hypertrophic Obstructive Cardiomyopathy
  • HYPERTR OBSTR CARDIOMYOP
  • hyper. obst. cardiomyopathy
  • SUBVALV STENOSIS
  • HCM - Hypertrophic cardiomyopathy
  • IDIOPATHIC HYPERTROPHIC SUBVALV STENOSIS
  • Obstructive Cardiomyopathy, Hypertrophic
  • Hypertrophies, Asymmetric Septal
  • Hypertrophic Cardiomyopathies
  • Cardiomyopathies, Hypertrophic Obstructive
  • Hypertrophic cardiomyopathy (disorder)
  • HOCM - Hypertrophic obstructive cardiomyopathy
  • Primary hypertrophic cardiomyopathy
  • Idiopathic Hypertrophic Subvalvular Stenosis
  • IHSS
  • primary hypertrophic cardiomyopathy (disorder) [Ambiguous]
  • Idiopathic Hypertrophic Subaortic Stenosis
  • Obstructive cardiomyopathy
  • SUBVALV STENOSIS IDIOPATHIC HYPERTROPHIC
  • Hypertrophy, Asymmetric Septal
  • Hypertrophic obstructive cardiomyopathy (disorder)
  • Septal Hypertrophy, Asymmetric
  • Cardiomyopathies, Hypertrophic
  • IHSSs
  • hypertrophic myocardiopathy
  • Cardiomyopathy, Hypertrophic Obstructive
  • HCM
  • Obstructive Cardiomyopathies, Hypertrophic
  • Asymmetric Septal Hypertrophy
  • Septal Hypertrophies, Asymmetric
  • hypertrophic subaortic stenosis
  • obstructive hypertrophic cardiomyopathy
  • hypertrophic obstructive cardiomyopathy
  • hypertrophic cardiomyopathy
  • familial hypertrophic cardiomyopathy
  • HCM - hypertrophic cardiomyopathy
show more synonyms
Genetic variants
JPH2 (target)
q13.12.
NM_020433.5:c.482C>A
NP_065166.2:p.(Thr161Lys)
Heterozygous
JPH2 mutation c.482C>A (p.T161K)

Karyotyping (Donor)

Has the donor karyotype been analysed?
No

Other Genotyping (Donor)

Is there genome-wide genotyping or functional data available?
No

External Databases (Donor)

BioSamples SAMEA6880674

Ethics

Also have a look at the ethics information for the parental line TAUi001-A .
For generation of the cell line, who was the supplier of any recombined DNA vectors or commercial kits used?

hIPSC Derivation

General

The source cell information can be found in the parental cell line TAUi001-A.

Reprogramming method

Vector type Non-integrating
Vector Episomal
Genes
Is reprogramming vector detectable?
No

Vector free reprogramming

Type of used vector free reprogramming factor(s)
None

Other

Derived under xeno-free conditions
No
Derived under GMP?
No
Available as clinical grade?
No

Culture Conditions

Surface coating Matrigel/Geltrex
Feeder cells
No
Passage method Enzymatically
Versene
CO2 Concentration 5 %
Medium mTeSR™ 1
Supplements
Pen/Strep %
Has Rock inhibitor (Y27632) been used at passage previously with this cell line?
No
Has Rock inhibitor (Y27632) been used at cryo previously with this cell line?
Yes
Has Rock inhibitor (Y27632) been used at thaw previously with this cell line?
No

Characterisation

Analysis of Undifferentiated Cells
Marker Expressed Immunostaining RT-PCR Flow Cytometry Enzymatic Assay Expression Profiles
POU5F1 (OCT-4)
Yes
SOX2
Yes
NANOG
Yes
ZFP42 (REX-1)
Yes
C-MYC
Yes
Differentiation Potency
Endoderm
Ont Id: UBERON_0000925
In vitro spontaneous differentiation
Marker Expressed
SOX17
Yes
AFP
Yes
Protocol or reference
Mesoderm
Ont Id: UBERON_0000926
In vitro spontaneous differentiation
Marker Expressed
KDR
Yes
ACTC1 / alpha cardiac actinin
Yes
Protocol or reference
Ectoderm
Ont Id: UBERON_0000924
In vitro spontaneous differentiation
Marker Expressed
SOX1
Yes
PAX6
Yes
Protocol or reference

Genotyping

Karyotyping (Cell Line)

Has the cell line karyotype been analysed?
No

Other Genotyping (Cell Line)

Genetic Modification

Genetic modifications not related to a disease
JPH2 (target)
Isogenic modification
q13.12.
NM_020433.5:c.482A>C
NP_065166.2:p.(Lys161Thr)
Heterozygous
Repaired