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Cellosaurus ZZUNEUi007-A (CVCL_YB90)

[Text version]
Cell line name ZZUNEUi007-A
Accession CVCL_YB90
Resource Identification Initiative To cite this cell line use: ZZUNEUi007-A (RRID:CVCL_YB90)
Comments From: Zhengzhou University First Affiliated Hospital; Zhengzhou; China.
Population: Chinese; Han.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations
  • Mutation; HGNC; 7577; MYH7; Simple; p.Arg663His (c.1988G>A); ClinVar=VCV000042875; Zygosity=Heterozygous (PubMed=31931472).
Disease Familial hypertrophic cardiomyopathy type 1 (NCIt: C172092)
Rare familial disorder with hypertrophic cardiomyopathy (ORDO: Orphanet_99739)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Female
Age at sampling 26Y
Category Induced pluripotent stem cell

PubMed=31931472; DOI=10.1016/j.scr.2020.101699
Li X.-W., Liu Y.-Y., Liu F.-F., Wang X.-J., Liu M.-D., Du W.-T., Zhao J., Wang M.-Y., Hu L., Wang C.-C., Fu W.-R., Dong J.-Z., Zhao X.-Y.
Generation of a hiPSC line ZZUNEUi007-A from a patient with hypertrophic cardiomyopathy caused by mutation in MYH7.
Stem Cell Res. 43:101699-101699(2020)

Cell line databases/resources hPSCreg; ZZUNEUi007-A
SKIP; SKIP005644
Encyclopedic resources Wikidata; Q98136724
Entry history
Entry creation19-Dec-2019
Last entry update29-Jun-2023
Version number9