GABRB3
From Wikipedia, the free encyclopedia
Gamma-aminobutyric acid (GABA) A receptor, beta 3
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Identifiers | ||||||||||||||
Symbol(s) | GABRB3; MGC9051 | |||||||||||||
External IDs | OMIM: 137192 MGI: 95621 HomoloGene: 633 | |||||||||||||
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RNA expression pattern | ||||||||||||||
Orthologs | ||||||||||||||
Human | Mouse | |||||||||||||
Entrez | 2562 | 14402 | ||||||||||||
Ensembl | ENSG00000166206 | ENSMUSG00000033676 | ||||||||||||
Uniprot | P28472 | P63080 | ||||||||||||
Refseq | NM_000814 (mRNA) NP_000805 (protein) |
NM_001038701 (mRNA) NP_001033790 (protein) |
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Location | Chr 15: 24.34 - 24.77 Mb | Chr 7: 57.46 - 57.7 Mb | ||||||||||||
Pubmed search | [1] | [2] |
Gamma-aminobutyric acid (GABA) A receptor, beta 3, also known as GABRB3, is a human gene.
This gene encodes a member of the ligand-gated ionic channel family. The encoded protein is one of at least 13 distinct subunits of a multisubunit chloride channel that serves as the receptor for gamma-aminobutyric acid, the major inhibitory transmitter of the nervous system. This gene is located on the long arm of chromosome 15 in a cluster with two genes encoding related subunits of the family. Mutations in this gene may be associated with the pathogenesis of Angelman syndrome, Prader-Willi syndrome, and autism. Alternatively spliced transcript variants encoding isoforms with distinct signal peptides have been described.[1]
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[edit] See also
[edit] References
[edit] Further reading
- Saitoh S, Kubota T, Ohta T, et al. (1992). "Familial Angelman syndrome caused by imprinted submicroscopic deletion encompassing GABAA receptor beta 3-subunit gene.". Lancet 339 (8789): 366–7. PMID 1346439.
- Wagstaff J, Chaillet JR, Lalande M (1992). "The GABAA receptor beta 3 subunit gene: characterization of a human cDNA from chromosome 15q11q13 and mapping to a region of conserved synteny on mouse chromosome 7.". Genomics 11 (4): 1071–8. PMID 1664410.
- Wagstaff J, Knoll JH, Fleming J, et al. (1991). "Localization of the gene encoding the GABAA receptor beta 3 subunit to the Angelman/Prader-Willi region of human chromosome 15.". Am. J. Hum. Genet. 49 (2): 330–7. PMID 1714232.
- Russek SJ, Farb DH (1995). "Mapping of the beta 2 subunit gene (GABRB2) to microdissected human chromosome 5q34-q35 defines a gene cluster for the most abundant GABAA receptor isoform.". Genomics 23 (3): 528–33. doi: . PMID 7851879.
- Knoll JH, Cheng SD, Lalande M (1994). "Allele specificity of DNA replication timing in the Angelman/Prader-Willi syndrome imprinted chromosomal region.". Nat. Genet. 6 (1): 41–6. doi: . PMID 8136833.
- Tögel M, Mossier B, Fuchs K, Sieghart W (1994). "gamma-Aminobutyric acidA receptors displaying association of gamma 3-subunits with beta 2/3 and different alpha-subunits exhibit unique pharmacological properties.". J. Biol. Chem. 269 (17): 12993–8. PMID 8175718.
- Kirkness EF, Fraser CM (1993). "A strong promoter element is located between alternative exons of a gene encoding the human gamma-aminobutyric acid-type A receptor beta 3 subunit (GABRB3).". J. Biol. Chem. 268 (6): 4420–8. PMID 8382702.
- Sinnett D, Wagstaff J, Glatt K, et al. (1993). "High-resolution mapping of the gamma-aminobutyric acid receptor subunit beta 3 and alpha 5 gene cluster on chromosome 15q11-q13, and localization of breakpoints in two Angelman syndrome patients.". Am. J. Hum. Genet. 52 (6): 1216–29. PMID 8389098.
- Glatt K, Glatt H, Lalande M (1997). "Structure and organization of GABRB3 and GABRA5.". Genomics 41 (1): 63–9. doi: . PMID 9126483.
- Meguro M, Mitsuya K, Sui H, et al. (1997). "Evidence for uniparental, paternal expression of the human GABAA receptor subunit genes, using microcell-mediated chromosome transfer.". Hum. Mol. Genet. 6 (12): 2127–33. PMID 9328477.
- Russek SJ (1999). "Evolution of GABA(A) receptor diversity in the human genome.". Gene 227 (2): 213–22. PMID 10023064.
- Buckley ST, Eckert AL, Dodd PR (2006). "Expression and distribution of GABAA receptor subtypes in human alcoholic cerebral cortex.". Ann. N. Y. Acad. Sci. 914: 58–64. PMID 11085308.
- Scapoli L, Martinelli M, Pezzetti F, et al. (2002). "Linkage disequilibrium between GABRB3 gene and nonsyndromic familial cleft lip with or without cleft palate.". Hum. Genet. 110 (1): 15–20. doi: . PMID 11810291.
- Buxbaum JD, Silverman JM, Smith CJ, et al. (2002). "Association between a GABRB3 polymorphism and autism.". Mol. Psychiatry 7 (3): 311–6. doi: . PMID 11920158.
- Buhr A, Bianchi MT, Baur R, et al. (2002). "Functional characterization of the new human GABA(A) receptor mutation beta3(R192H).". Hum. Genet. 111 (2): 154–60. doi: . PMID 12189488.
- Trudell J (2002). "Unique assignment of inter-subunit association in GABA(A) alpha 1 beta 3 gamma 2 receptors determined by molecular modeling.". Biochim. Biophys. Acta 1565 (1): 91–6. PMID 12225856.
- Sarto I, Wabnegger L, Dögl E, Sieghart W (2002). "Homologous sites of GABA(A) receptor alpha(1), beta(3) and gamma(2) subunits are important for assembly.". Neuropharmacology 43 (4): 482–91. PMID 12367595.
- Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences.". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. doi: . PMID 12477932.
- Słopień A, Rajewski A, Budny B, Czerski P (2003). "[Evaluation of q11-q13 locus of chromosome 15 aberrations and polymorphisms in the B3 subunit of the GABA-A receptor gene (GABRB3) in autistic patients]". Psychiatr. Pol. 36 (5): 779–91. PMID 12491987.
- Brandon NJ, Jovanovic JN, Colledge M, et al. (2003). "A-kinase anchoring protein 79/150 facilitates the phosphorylation of GABA(A) receptors by cAMP-dependent protein kinase via selective interaction with receptor beta subunits.". Mol. Cell. Neurosci. 22 (1): 87–97. PMID 12595241.
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This article incorporates text from the United States National Library of Medicine, which is in the public domain.
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