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Cellosaurus WAe009-A-69 (CVCL_B0FR)

[Text version]
Cell line name WAe009-A-69
Synonyms MYH7-KO; ANZHENe010-A-69
Accession CVCL_B0FR
Resource Identification Initiative To cite this cell line use: WAe009-A-69 (RRID:CVCL_B0FR)
Comments From: Anzhen Hospital, Capital Medical University; Beijing; China.
Knockout cell: Method=CRISPR/Cas9; HGNC; 7577; MYH7.
Derived from site: In situ; Blastocyst; UBERON=UBERON_0000358.
Cell type: Embryonic stem cell; CL=CL_0002322.
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)
Hierarchy Parent: CVCL_9773 (WA09)
Sex of cell Female
Age at sampling Blastocyst stage
Category Embryonic stem cell

PubMed=34678661; DOI=10.1016/j.scr.2021.102566
Guo T.-W., Jiang Y.-X., Song Y.-X., Ma S.-H., Chang Y., Zhang S.-Y., Wang H.-Y., Dong T., Jiang H.-F., Lu W.-J.
Generation of a homozygous MYH7 gene knockout human embryonic stem cell line (WAe009-A-69) using an episomal vector-based CRISPR/Cas9 system.
Stem Cell Res. 57:102566-102566(2021)

Cell line databases/resources hPSCreg; WAe009-A-69
Biological sample resources BioSamples; SAMEA9787090
Encyclopedic resources Wikidata; Q108821509
Entry history
Entry creation23-Sep-2021
Last entry update29-Jun-2023
Version number5