ID   Abcc8-A4
AC   CVCL_A4GR
DR   Wikidata; Q105506051
RX   PubMed=27934599;
CC   From: Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences; Guangzhou; China.
CC   Knockout cell: Method=CRISPR/Cas9; HGNC; 59; ABCC8.
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: 29-06-23; Version: 5
//
RX   PubMed=27934599; DOI=10.1016/j.scr.2016.11.011;
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 homozygous mutation human embryonic stem cell
RT   line using CRISPR/Cas9.";
RL   Stem Cell Res. 17:640-642(2016).
//