Cellosaurus cell line ZW-hiPSC 9 (CVCL

Cross-references
Cell line name	ZW-hiPSC 9
Synonyms	ZW9
Accession	CVCL_A4HA
Resource Identification Initiative	To cite this cell line use: ZW-hiPSC 9 (RRID:CVCL_A4HA)
Comments	From: Department of Physiology and Pathophysiology, School of Basic Medical Sciences, Fudan University; Shanghai; China. Population: Chinese. Derived from site: In situ; Skin, dermis; UBERON=UBERON_0002067. Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations	Mutation; HGNC; HGNC:9386; PRKAG2; Simple; p.Arg302Gln (c.905G>A); ClinVar=VCV000006846; Zygosity=Heterozygous (PubMed=29452156).
Disease	Familial hypertrophic cardiomyopathy type 6 (NCIt: C177249) Rare familial disorder with hypertrophic cardiomyopathy (ORDO: Orphanet_99739)
Species of origin	Homo sapiens (Human) (NCBI Taxonomy: 9606)
Originate from same individual	CVCL_A4GZ ! ZW-hiPSC 6 CVCL_A4HB ! ZW-hiPSC 12
Sex of cell	Male
Age at sampling	28Y
Category	Induced pluripotent stem cell
Publications	PubMed=29452156; DOI=10.1016/j.yjmcc.2018.02.007 Zhan Y.-K., Sun X.-L., Li B., Cai H.-H., Xu C., Liang Q.-Q., Lu C., Qian R.-Z., Chen S.-F., Yin L.-H., Sheng W., Huang G.-Y., Sun A.-J., Ge J.-B., Sun N. Establishment of a PRKAG2 cardiac syndrome disease model and mechanism study using human induced pluripotent stem cells. J. Mol. Cell. Cardiol. 117:49-61(2018)
Cell line databases/resources	SKIP; SKIP003132
Encyclopedic resources	Wikidata; Q105511875
Entry history
Entry creation	12-Jan-2021
Last entry update	19-Dec-2024
Version number	6