General

Cell Line

hPSCreg name SCVIi078-A
Cite as:
SCVIi078-A (RRID:CVCL_C7YG)
Cell line type Human induced pluripotent stem cell (hiPSC)
Similar lines
UKKi007-A
(NP0014-6, UKK007Ai)
Donor's gene variants:
RYR2, RYR2
Donor diseases:
Catecholaminergic polymorphic ventricular tachycardia
UKKi007-B
(NP0014-5)
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RYR2
Donor diseases:
Catecholaminergic polymorphic ventricular tachycardia
TAUi005-A
(UTA.14511.CPVT)
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RYR2
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Catecholaminergic polymorphic ventricular tachycardia
TAUi004-A
(UTA.05208.CPVT)
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RYR2
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SCVIi091-A
(SCVI2617)
Donor diseases:
transthyretin amyloidosis
FAMRCi005-A
(LMNA B4)
Donor's gene variants:
LMNA
Donor diseases:
myopathy
atrioventricular block
Paroxysmal ventricular tachycardia
FAMRCi005-B
(LMNA B5)
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LMNA
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myopathy
atrioventricular block
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KMUGMCi001-A
(KMUGMCi001ACVRL1)
Donor diseases:
Telangiectasia, Hereditary Hemorrhagic
UKKi030-A
(NP0134-6D)
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SCN5A
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Brugada syndrome
UKKi030-B
(NP0134-18A)
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SCN5A
Donor diseases:
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UKKi030-C
(NP0134-26B)
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SCN5A
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UKKi024-A
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Brugada syndrome
UKKi024-B
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Brugada syndrome
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(NP0133-4)
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Brugada syndrome
KMUGMCi005-A
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Epidermodysplasia Verruciformis
ISMMSi046-A
(PLN-R14del-3BC7)
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KMUGMCi004-A
(KMUGMCi004APC, KN615)
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familial adenomatous polyposis
SCVIi073-A
(SCVIi574C2)
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titin, BAG cochaperone 3, BAG cochaperone 3
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Dilated Cardiomyopathy
SCVIi061-A
(SCVI2149C1)
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(SCVIi599C1)
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BAG cochaperone 3
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Hypertrophic Cardiomyopathy
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(SCVI2150c1)
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AIBNi016-A
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hereditary spastic paraplegia 56
PUMCHi002-A
(20180908R-AE3, PUMCH-IRC)
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Restrictive Cardiomyopathy
ITXi004-A
(MS381)
Donor diseases:
Long QT Syndrome
FAMRCi006-A
(LMNA T3)
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LMNA
Donor diseases:
Emery-Dreifuss Muscular Dystrophy
Dilated Cardiomyopathy
FAMRCi006-B
(LMNA T4)
Donor's gene variants:
LMNA
Donor diseases:
Emery-Dreifuss Muscular Dystrophy
Dilated Cardiomyopathy
UKKi031-A
(NP0138-8B)
Donor's gene variants:
TNNT2
Donor diseases:
Rare hypertrophic cardiomyopathy
UKKi031-B
(NP0138-19E)
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TNNT2
Donor diseases:
Rare hypertrophic cardiomyopathy
ZJSHi001-A
(ZJSHi-KCNB1)
Donor's gene variants:
KCNB1
Donor diseases:
developmental and epileptic encephalopathy, 26
UKKi031-C
(NP0138-31B)
Donor's gene variants:
TNNT2
Donor diseases:
Rare hypertrophic cardiomyopathy
CABi003-A
(DH05, AMDdh05-MiPS4F16)
Donor diseases:
Age-Related Macular Degeneration
USFi003-A
(1AB1)
Donor diseases:
Dilated Cardiomyopathy
Last update 12th August 2023
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Provider

Generator Stanford Cardiovascular Institute (SCVI)
Owner Stanford Cardiovascular Institute (SCVI)
Distributors
Derivation country United States

External Databases

Cellosaurus CVCL_C7YG
BioSamples SAMEA114260510
Wikidata Q123033418

General Information

Publications
* Is the cell line readily obtainable for third parties?
Yes
Research use: allowed
Clinical use: not allowed
Commercial use: not allowed

Donor Information

General Donor Information

Sex female
Ethnicity Non-Hispanic or Latino

Phenotype and Disease related information (Donor)

Diseases A disease was diagnosed.
Synonyms
  • CPVT
  • bidirectional tachycardia induced by catecholamine
  • catecholaminergic polymorphic ventricular tachycardia
  • double tachycardia induced by catecholamines
  • malignant paroxysmal ventricular tachycardia
  • multifocal ventricular premature beats
  • ventricular tachycardia, catecholaminergic polymorphic
  • catecholamine-induced polymorphic ventricular tachycardia
  • familial polymorphic ventricular tachycardia
  • polymorphic catecholergic ventricular tachycardia
  • stress-induced polymorphic ventricular tachycardia
  • syncopal paroxysmal tachycardia
show more synonyms

External Databases (Donor)

BioSamples SAMEA114260511

Ethics

Has informed consent been obtained from the donor of the embryo/tissue from which the pluripotent stem cells have been derived? Yes
Was the consent voluntarily given? Yes
Has the donor been informed that participation will not directly influence their personal treatment? Yes
Can you provide us with a copy of the Donor Information Sheet provided to the donor? No
Please provide contact information of the holder of the original Donor Information Sheet. yanzhuge@stanford.edu
Do you (Depositor/Provider) hold the original Donor Consent Form? Yes
Please indicate whether the data associated with the donated material has been pseudonymised or anonymised. pseudonymised
Does consent explicitly allow the derivation of pluripotent stem cells? Yes
Does consent prevent CELLS DERIVED FROM THE DONATED BIOSAMPLE from being made available to researchers anywhere in the world? Yes
How may genetic information associated with the cell line be accessed? Controlled Access
Will the donor expect to receive financial benefit, beyond reasonable expenses, in return for donating the biosample? No
Has a favourable opinion been obtained from a research ethics committee, or other ethics review panel, in relation to the Research Protocol including the consent provisions? No
For generation of the cell line, who was the supplier of any recombined DNA vectors or commercial kits used?

hIPSC Derivation

General

Source cell type
A peripheral blood cell with a single nucleus. This category includes lymphocytes and monocytes.
Synonyms
  • PERIPHERAL BLOOD MONONUCLEAR CELL
  • Peripheral Blood Mononuclear Cell
  • PBMC

Reprogramming method

Vector type Non-integrating
Vector Sendai virus

Vector free reprogramming

Other

Derived under xeno-free conditions
Unknown
Derived under GMP?
Unknown
Available as clinical grade?
Unknown

Culture Conditions

Medium StemPro® hESC SFM

Characterisation

Analysis of Undifferentiated Cells
Marker Expressed Immunostaining RT-PCR Flow Cytometry Enzymatic Assay Expression Profiles
SOX2
Yes
NANOG
Yes
POU5F1 (OCT-4)
Yes
Morphology pictures
Differentiation Potency
Endoderm
Ont Id: UBERON_0000925
In vitro directed differentiation
Morphology
Mesoderm
Ont Id: UBERON_0000926
In vitro directed differentiation
Morphology
Ectoderm
Ont Id: UBERON_0000924
In vitro directed differentiation
Morphology

Genotyping

Karyotyping (Cell Line)

Has the cell line karyotype been analysed?
Yes
CN=2, Female normal karyotype
Passage number: 12

Other Genotyping (Cell Line)