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Cellosaurus H9SNTA1KO (CVCL_C5TU)

[Text version]
Cell line name H9SNTA1KO
Accession CVCL_C5TU
Resource Identification Initiative To cite this cell line use: H9SNTA1KO (RRID:CVCL_C5TU)
Comments From: Qiqihar Institute of Medical and Pharmaceutical Sciences, Qiqihar Medical University; Qiqihar; China.
Knockout cell: Method=CRISPR/Cas9; HGNC; 11167; SNTA1.
Caution: There seems to be two H9SNTA1KO cell line established in China, this one and CVCL_A5EP.
Derived from site: In situ; Blastocyst; UBERON=UBERON_0000358.
Cell type: Embryonic stem cell; CL=CL_0002322.
Disease Long QT syndrome 12 (NCIt: C192202)
Familial long QT syndrome (ORDO: Orphanet_768)
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
Publications

PubMed=35773684; DOI=10.1186/s13287-022-02955-4
Dong T., Zhao Y., Jin H.-F., Shen L., Lin Y., Si L.-L., Chen L., Liu J.-C.
SNTA1-deficient human cardiomyocytes demonstrate hypertrophic phenotype and calcium handling disorder.
Stem Cell Res. Ther. 13:288.1-288.19(2022)

Cross-references
Encyclopedic resources Wikidata; Q116049279
Entry history
Entry creation15-Dec-2022
Last entry update29-Jun-2023
Version number3