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Cellosaurus WAe009-A-46 (CVCL_A4UC)

[Text version]

Cell line name WAe009-A-46
Synonyms LCSPHe001-A-46
Accession CVCL_A4UC
Resource Identification Initiative To cite this cell line use: WAe009-A-46 (RRID:CVCL_A4UC)
Comments From: The Second People's Hospital of Liaocheng; Liaocheng; China.
Knockout cell: Method=CRISPR/Cas9; HGNC; 7576; MYH6.
Disease Familial hypertrophic cardiomyopathy type 14 (NCIt: C176899)
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=33360099; DOI=10.1016/j.scr.2020.102128
Hao E.-G., Zhang G.-H., Mu L.-H., Ma N.-N., Wang T.
Establishment of a human MYH6 compound heterozygous knockout hESC line to model cardiomyopathy and congenital heart defects by CRISPR/Cas9 system.
Stem Cell Res. 50:102128-102128(2021)

Cell line databases/resources hPSCreg; WAe009-A-46
Encyclopedic resources Wikidata; Q107117419
Entry history
Entry creation20-May-2021
Last entry update23-Sep-2021
Version number2