Cellosaurus Abcc8-A2 (CVCL_A4GW)
| Cell line name | Abcc8-A2 |
|---|---|
| Accession | CVCL_A4GW |
| Resource Identification Initiative | To cite this cell line use: Abcc8-A2 (RRID:CVCL_A4GW) |
| Comments | From: Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences; Guangzhou; China. Knockout cell: Method=CRISPR/Cas9; HGNC; HGNC:59; ABCC8 (Note=1 of 2 alleles). Derived from site: In situ; Blastocyst; UBERON=UBERON_0000358. Cell type: Embryonic stem cell; CL=CL_0002322. |
| Disease | Persistent hyperinsulinemic hypoglycemia of infancy (NCIt: C122923) Autosomal dominant hyperinsulinism due to SUR1 deficiency (ORDO: Orphanet_276575) |
| Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) |
| Hierarchy | Parent: CVCL_9771 (WA01) |
| Sex of cell | Male |
| Age at sampling | Blastocyst stage |
| Category | Embryonic stem cell |
| Publications | PubMed=27934605; DOI=10.1016/j.scr.2016.11.014 |
| Cross-references | |
| Encyclopedic resources | Wikidata; Q105506049 |
| Entry history | |
| Entry creation | 12-Jan-2021 |
| Last entry update | 19-Dec-2024 |
| Version number | 7 |