GAD2

Glutamate decarboxylase 2 (pancreatic islets and brain, 65kDa)

PDB rendering based on 2okk.
Identifiers
Symbols GAD2; GAD65; MGC161605; MGC161607
External IDs OMIM138275 MGI95634 HomoloGene20223 GeneCards: GAD2 Gene
EC number 4.1.1.15
RNA expression pattern
More reference expression data
Orthologs
Species Human Mouse
Entrez 2572 14417
Ensembl ENSG00000136750 ENSMUSG00000026787
UniProt Q05329 Q3URJ3
RefSeq (mRNA) NM_000818.2 NM_008078.2
RefSeq (protein) NP_000809.1 NP_032104.2
Location (UCSC) Chr 10:
26.51 – 26.59 Mb
Chr 2:
22.48 – 22.55 Mb
PubMed search [1] [2]

Glutamate decarboxylase 2 is an enzyme that in humans is encoded by the GAD2 gene.[1]

This gene encodes one of several forms of glutamic acid decarboxylase, identified as a major autoantigen in insulin-dependent diabetes. The enzyme encoded is responsible for catalyzing the production of gamma-aminobutyric acid from L-glutamic acid. A pathogenic role for this enzyme has been identified in the human pancreas since it has been identified as an autoantibody and an autoreactive T cell target in insulin-dependent diabetes. This gene may also play a role in the stiff man syndrome.[2]

See also

Interactions

GAD2 has been shown to interact with GAD1.[3]

References

  1. ^ Cram DS, Barnett LD, Joseph JL, Harrison LC (Jul 1991). "Cloning and partial nucleotide sequence of human glutamic acid decarboxylase cDNA from brain and pancreatic islets". Biochem Biophys Res Commun 176 (3): 1239–44. doi:10.1016/0006-291X(91)90418-7. PMID 2039509. 
  2. ^ "Entrez Gene: GAD2 glutamate decarboxylase 2 (pancreatic islets and brain, 65kDa)". http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=2572. 
  3. ^ Dirkx, R; Thomas A, Li L, Lernmark A, Sherwin R S, De Camilli P, Solimena M (Feb. 1995). "Targeting of the 67-kDa isoform of glutamic acid decarboxylase to intracellular organelles is mediated by its interaction with the NH2-terminal region of the 65-kDa isoform of glutamic acid decarboxylase". J. Biol. Chem. (UNITED STATES) 270 (5): 2241–6. doi:10.1074/jbc.270.5.2241. ISSN 0021-9258. PMID 7836456. 

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