ABCC8

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ATP-binding cassette, sub-family C (CFTR/MRP), member 8
Identifiers
Symbol(s) ABCC8; PHHI; MRP8; ABC36; HHF1; HI; HRINS; SUR; SUR1; TNDM2
External IDs OMIM: 600509 MGI1352629 Homologene68048
RNA expression pattern

PBB GE ABCC8 210246 s at tn.png

More reference expression data

Orthologs
Human Mouse
Entrez 6833 20927
Ensembl ENSG00000006071 ENSMUSG00000040136
Uniprot Q09428 na
Refseq NM_000352 (mRNA)
NP_000343 (protein)
NM_011510 (mRNA)
NP_035640 (protein)
Location Chr 11: 17.37 - 17.46 Mb Chr 7: 45.97 - 46.05 Mb
Pubmed search [1] [2]

ATP-binding cassette, sub-family C (CFTR/MRP), member 8, also known as ABCC8, is a human gene.


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, an autosomal dominant disease of defective insulin secretion. Alternative splicing of this gene has been observed; however, the transcript variants have not been fully described.[1]


See also

Sulfonylurea receptor

References

Further reading

  • Aguilar-Bryan L, Bryan J (1999). "Molecular biology of adenosine triphosphate-sensitive potassium channels.". Endocr. Rev. 20 (2): 101–35. PMID 10204114. 
  • Meissner T, Beinbrech B, Mayatepek E (1999). "Congenital hyperinsulinism: molecular basis of a heterogeneous disease.". Hum. Mutat. 13 (5): 351–61. PMID 10338089. doi:10.1002/(SICI)1098-1004(1999)13:5<351::AID-HUMU3>3.0.CO;2-R. 
  • Gloyn AL, Siddiqui J, Ellard S (2006). "Mutations in the genes encoding the pancreatic beta-cell KATP channel subunits Kir6.2 (KCNJ11) and SUR1 (ABCC8) in diabetes mellitus and hyperinsulinism.". Hum. Mutat. 27 (3): 220–31. PMID 16416420. doi:10.1002/humu.20292. 
  • Bryan J, Muñoz A, Zhang X; et al. (2007). "ABCC8 and ABCC9: ABC transporters that regulate K+ channels.". Pflugers Arch. 453 (5): 703–18. PMID 16897043. doi:10.1007/s00424-006-0116-z. 
  • Inagaki N, Gonoi T, Clement JP; et al. (1996). "Reconstitution of IKATP: an inward rectifier subunit plus the sulfonylurea receptor.". Science. 270 (5239): 1166–70. PMID 7502040. 
  • Aguilar-Bryan L, Nichols CG, Wechsler SW; et al. (1995). "Cloning of the beta cell high-affinity sulfonylurea receptor: a regulator of insulin secretion.". Science. 268 (5209): 423–6. PMID 7716547. 
  • Thomas PM, Cote GJ, Wohllk N; et al. (1995). "Mutations in the sulfonylurea receptor gene in familial persistent hyperinsulinemic hypoglycemia of infancy.". Science. 268 (5209): 426–9. PMID 7716548. 
  • Thomas PM, Cote GJ, Hallman DM, Mathew PM (1995). "Homozygosity mapping, to chromosome 11p, of the gene for familial persistent hyperinsulinemic hypoglycemia of infancy.". Am. J. Hum. Genet. 56 (2): 416–21. PMID 7847376. 
  • Glaser B, Chiu KC, Anker R; et al. (1994). "Familial hyperinsulinism maps to chromosome 11p14-15.1, 30 cM centromeric to the insulin gene.". Nat. Genet. 7 (2): 185–8. PMID 7920639. doi:10.1038/ng0694-185. 
  • Inagaki N, Gonoi T, Clement JP; et al. (1996). "A family of sulfonylurea receptors determines the pharmacological properties of ATP-sensitive K+ channels.". Neuron. 16 (5): 1011–7. PMID 8630239. 
  • Inoue H, Ferrer J, Welling CM; et al. (1996). "Sequence variants in the sulfonylurea receptor (SUR) gene are associated with NIDDM in Caucasians.". Diabetes. 45 (6): 825–31. PMID 8635661. 
  • Nichols CG, Shyng SL, Nestorowicz A; et al. (1996). "Adenosine diphosphate as an intracellular regulator of insulin secretion.". Science. 272 (5269): 1785–7. PMID 8650576. 
  • Thomas PM, Wohllk N, Huang E; et al. (1996). "Inactivation of the first nucleotide-binding fold of the sulfonylurea receptor, and familial persistent hyperinsulinemic hypoglycemia of infancy.". Am. J. Hum. Genet. 59 (3): 510–8. PMID 8751851. 
  • Nestorowicz A, Wilson BA, Schoor KP; et al. (1997). "Mutations in the sulonylurea receptor gene are associated with familial hyperinsulinism in Ashkenazi Jews.". Hum. Mol. Genet. 5 (11): 1813–22. PMID 8923011. 
  • Dunne MJ, Kane C, Shepherd RM; et al. (1997). "Familial persistent hyperinsulinemic hypoglycemia of infancy and mutations in the sulfonylurea receptor.". N. Engl. J. Med. 336 (10): 703–6. PMID 9041101. 
  • Gribble FM, Tucker SJ, Ashcroft FM (1997). "The essential role of the Walker A motifs of SUR1 in K-ATP channel activation by Mg-ADP and diazoxide.". EMBO J. 16 (6): 1145–52. PMID 9135131. doi:10.1093/emboj/16.6.1145. 
  • Ohta Y, Tanizawa Y, Inoue H; et al. (1998). "Identification and functional analysis of sulfonylurea receptor 1 variants in Japanese patients with NIDDM.". Diabetes. 47 (3): 476–81. PMID 9519757. 
  • Hansen T, Echwald SM, Hansen L; et al. (1998). "Decreased tolbutamide-stimulated insulin secretion in healthy subjects with sequence variants in the high-affinity sulfonylurea receptor gene.". Diabetes. 47 (4): 598–605. PMID 9568693. 
  • Nestorowicz A, Glaser B, Wilson BA; et al. (1999). "Genetic heterogeneity in familial hyperinsulinism.". Hum. Mol. Genet. 7 (7): 1119–28. PMID 9618169. 
  • Shyng SL, Ferrigni T, Shepard JB; et al. (1998). "Functional analyses of novel mutations in the sulfonylurea receptor 1 associated with persistent hyperinsulinemic hypoglycemia of infancy.". Diabetes. 47 (7): 1145–51. PMID 9648840. 
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Template:Membrane-protein-stub This article incorporates text from the United States National Library of Medicine, which is in the public domain.


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