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Cellosaurus ZW-hiPSC 12 (CVCL_A4HB)

[Text version]
Cell line name ZW-hiPSC 12
Synonyms ZW12
Accession CVCL_A4HB
Resource Identification Initiative To cite this cell line use: ZW-hiPSC 12 (RRID:CVCL_A4HB)
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
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)
Hierarchy Children:
CVCL_A4HI (ZW-C-hiPSC)
Originate from same individual CVCL_A4GZ ! ZW-hiPSC 6
CVCL_A4HA ! ZW-hiPSC 9
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)

Cross-references
Cell line databases/resources SKIP; SKIP003133
Encyclopedic resources Wikidata; Q105511871
Entry history
Entry creation12-Jan-2021
Last entry update19-Dec-2024
Version number6