ID   WAe009-A-46
AC   CVCL_A4UC
SY   LCSPHe001-A-46
DR   hPSCreg; WAe009-A-46
DR   Wikidata; Q107117419
RX   PubMed=33360099;
CC   From: The Second People's Hospital of Liaocheng; Liaocheng; China.
CC   Knockout cell: Method=CRISPR/Cas9; HGNC; 7576; MYH6.
CC   Derived from site: In situ; Blastocyst; UBERON=UBERON_0000358.
CC   Cell type: Embryonic stem cell; CL=CL_0002322.
DI   NCIt; C176899; Familial hypertrophic cardiomyopathy type 14
DI   ORDO; Orphanet_99739; Rare familial disorder with hypertrophic cardiomyopathy
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
HI   CVCL_9773 ! WA09
SX   Female
AG   Blastocyst stage
CA   Embryonic stem cell
DT   Created: 20-05-21; Last updated: 29-06-23; Version: 4
//
RX   PubMed=33360099; DOI=10.1016/j.scr.2020.102128;
RA   Hao E.-G., Zhang G.-H., Mu L.-H., Ma N.-N., Wang T.;
RT   "Establishment of a human MYH6 compound heterozygous knockout hESC
RT   line to model cardiomyopathy and congenital heart defects by
RT   CRISPR/Cas9 system.";
RL   Stem Cell Res. 50:102128-102128(2021).
//