ABCC8
Identifiers
AliasesABCC8, ABC36, HHF1, HI, HRINS, MRP8, PHHI, SUR, SUR1, SUR1delta2, TNDM2, ATP binding cassette subfamily C member 8, PNDM3
External IDsOMIM: 600509 MGI: 1352629 HomoloGene: 68048 GeneCards: ABCC8
Orthologs
SpeciesHumanMouse
Entrez

6833

20927

Ensembl

ENSG00000006071

ENSMUSG00000040136

UniProt

Q09428

n/a

RefSeq (mRNA)

NM_000352
NM_001287174
NM_001351295
NM_001351296
NM_001351297

NM_011510
NM_001357538

RefSeq (protein)

NP_000343
NP_001274103
NP_001338224
NP_001338225
NP_001338226

n/a

Location (UCSC)Chr 11: 17.39 – 17.48 MbChr 7: 45.75 – 45.83 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

ATP-binding cassette transporter sub-family C member 8 is a protein that in humans is encoded by the ABCC8 gene.[5][6] ABCC8 orthologs[7] have been identified in all mammals for which complete genome data are available.

The protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the MRP subfamily which is involved in multi-drug resistance. This protein functions as a modulator of ATP-sensitive potassium channels and insulin release. Mutations and deficiencies in this protein have been observed in patients with hyperinsulinemic hypoglycemia of infancy, an autosomal recessive disorder of unregulated and high insulin secretion. Mutations have also been associated with non-insulin-dependent diabetes mellitus type II (neonatal diabetes), an autosomal dominant disease of defective insulin secretion, and congenital hyperinsulinism.[8] Alternative splicing of this gene has been observed; however, the transcript variants have not been fully described.[9]

See also

References

  1. 1 2 3 GRCh38: Ensembl release 89: ENSG00000006071 - Ensembl, May 2017
  2. 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000040136 - Ensembl, May 2017
  3. ↑ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ↑ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ↑ Glaser B, Chiu KC, Anker R, Nestorowicz A, Landau H, Ben-Bassat H, et al. (June 1994). "Familial hyperinsulinism maps to chromosome 11p14-15.1, 30 cM centromeric to the insulin gene". Nature Genetics. 7 (2): 185–188. doi:10.1038/ng0694-185. PMID 7920639. S2CID 8681602.
  6. ↑ Thomas PM, Cote GJ, Wohllk N, Haddad B, Mathew PM, Rabl W, et al. (April 1995). "Mutations in the sulfonylurea receptor gene in familial persistent hyperinsulinemic hypoglycemia of infancy". Science. 268 (5209): 426–429. Bibcode:1995Sci...268..426T. doi:10.1126/science.7716548. PMID 7716548.
  7. ↑ "OrthoMaM phylogenetic marker: ABCC8 coding sequence". Archived from the original on 2015-09-24. Retrieved 2009-12-09.
  8. ↑ Kapoor RR, Flanagan SE, Arya VB, Shield JP, Ellard S, Hussain K (April 2013). "Clinical and molecular characterisation of 300 patients with congenital hyperinsulinism". European Journal of Endocrinology. 168 (4): 557–564. doi:10.1530/EJE-12-0673. PMC 3599069. PMID 23345197.
  9. ↑ "Entrez Gene: ABCC8 ATP-binding cassette, sub-family C (CFTR/MRP), member 8".

Further reading

This article incorporates text from the United States National Library of Medicine, which is in the public domain.

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