ID   Abcc8-A2
AC   CVCL_A4GW
DR   Wikidata; Q105506049
RX   PubMed=27934605;
CC   From: Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences; Guangzhou; China.
CC   Knockout cell: Method=CRISPR/Cas9; HGNC; 59; ABCC8 (Note=1 of 2 alleles).
CC   Derived from site: In situ; Blastocyst; UBERON=UBERON_0000358.
CC   Cell type: Embryonic stem cell; CL=CL_0002322.
DI   NCIt; C122923; Persistent hyperinsulinemic hypoglycemia of infancy
DI   ORDO; Orphanet_276575; Autosomal dominant hyperinsulinism due to SUR1 deficiency
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
HI   CVCL_9771 ! WA01
SX   Male
AG   Blastocyst stage
CA   Embryonic stem cell
DT   Created: 12-01-21; Last updated: 30-01-24; Version: 6
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RX   PubMed=27934605; DOI=10.1016/j.scr.2016.11.014;
RA   Guo D.-S., Liu H.-K., Gao G., Ruzi A., Wang K.-P., Wu H., Lai K.-Y.,
RA   Liu Y.-L., Yang F., Lai L.-X., Li Y.-X.;
RT   "Generation of an Abcc8 heterozygous mutation human embryonic stem
RT   cell line using CRISPR/Cas9.";
RL   Stem Cell Res. 17:670-672(2016).
//