Cellosaurus cell line SCVIi019-A (CVCL

Cross-references
Cell line name	SCVIi019-A
Synonyms	SCVI-744; SCVI 744; SCVI744
Accession	CVCL_B0PL
Resource Identification Initiative	To cite this cell line use: SCVIi019-A (RRID:CVCL_B0PL)
Comments	From: Stanford Cardiovascular Institute; Palo Alto; USA. Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Sequence variations	Mutation; HGNC; 11947; TNNI3; Simple; p.Arg79Cys (c.235C>T); ClinVar=VCV000043367; Zygosity=Heterozygous (PubMed=34798544).
Disease	Familial hypertrophic cardiomyopathy type 7 (NCIt: C184989) Rare familial disorder with hypertrophic cardiomyopathy (ORDO: Orphanet_99739)
Species of origin	Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell	Male
Age at sampling	23Y
Category	Induced pluripotent stem cell
Publications	PubMed=34798544; DOI=10.1016/j.scr.2021.102597; PMCID=PMC9095754 Zhao S.R., Shen M.-C., Lee C., Zha Y.-J., Guevara J.V., Wheeler M.T., Wu J.C. Generation of three induced pluripotent stem cell lines from hypertrophic cardiomyopathy patients carrying TNNI3 mutations. Stem Cell Res. 57:102597-102597(2021)
Cell line databases/resources	hPSCreg; SCVIi019-A
Encyclopedic resources	Wikidata; Q108821284
Entry history
Entry creation	23-Sep-2021
Last entry update	29-Jun-2023
Version number	4