ID   H9SNTA1KO
AC   CVCL_C5TU
DR   Wikidata; Q116049279
RX   PubMed=35773684;
CC   From: Qiqihar Institute of Medical and Pharmaceutical Sciences, Qiqihar Medical University; Qiqihar; China.
CC   Knockout cell: Method=CRISPR/Cas9; HGNC; 11167; SNTA1.
CC   Caution: There seems to be two H9SNTA1KO cell line established in China, this one and CVCL_A5EP.
CC   Derived from site: In situ; Blastocyst; UBERON=UBERON_0000358.
CC   Cell type: Embryonic stem cell; CL=CL_0002322.
DI   NCIt; C192202; Long QT syndrome 12
DI   ORDO; Orphanet_768; Familial long QT syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
HI   CVCL_9773 ! WA09
SX   Female
AG   Blastocyst stage
CA   Embryonic stem cell
DT   Created: 15-12-22; Last updated: 29-06-23; Version: 3
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RX   PubMed=35773684; DOI=10.1186/s13287-022-02955-4;
RA   Dong T., Zhao Y., Jin H.-F., Shen L., Lin Y., Si L.-L., Chen L.,
RA   Liu J.-C.;
RT   "SNTA1-deficient human cardiomyocytes demonstrate hypertrophic
RT   phenotype and calcium handling disorder.";
RL   Stem Cell Res. Ther. 13:288.1-288.19(2022).
//