Variant ID | 19076 |
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Entrez Gene ID | 2558 |
Gene | GABRA5 (GeneCards) |
Location | hg19 15:27137820-27137820
hg38 15:26892673-26892673 |
Disease | Asymptomatic |
Method | HiSeq X Ten |
Mutation(HGVS format) | NC_000015.9:g.27137820 C>T (Genome Assembly: GRCh37) |
Exon or Intron | NA |
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Position in protein | NA |
Amino acid changes in protein | NA > NA |
Position in cDNA | NA |
Changes in cDNA | NA > NA |
mRNA accession | NA |
mRNA length | NA |
Reference length | 102531392 |
MAF in gnomAD genome (version 2.0.1) | 0 |
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EIGEN score | -0.1185 |
CADD Raw score (version 1.3) | 0.851329 (Deleterious) |
FATHMM raw prediction score | 0.08871 (Tolerated) |
Deleterious probability by DeFine | 0.4025 (Neutral) |
Entrez Gene ID | 2558 (NCBI Gene) |
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Official Gene Symbol | GABRA5 (GeneCards) |
Number of variants in GABRA5 in this database | 4 (view all the variants) |
Full name | gamma-aminobutyric acid type A receptor alpha5 subunit |
Band | 15q12 |
Other IDs | Vega: OTTHUMG00000171824 OMIM: 137142 HGNC: HGNC:4079 Ensembl: ENSG00000186297 |
Other names | None |
Summary | GABA is the major inhibitory neurotransmitter in the mammalian brain where it acts at GABA-A receptors, which are ligand-gated chloride channels. Chloride conductance of these channels can be modulated by agents such as benzodiazepines that bind to the GABA-A receptor. At least 16 distinct subunits of GABA-A receptors have been identified. Transcript variants utilizing three different alternative non-coding first exons have been described. [provided by RefSeq, Jul 2008] |
Individual ID | 29217584.13 (view all the variants in this individual) |
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Pubmed ID | 29217584 |
Whose mosaic mutation | Normal |
Phenotype | 1 |
Disease | Asymptomatic |
OMIM ID |
Pubmed ID | 29217584 |
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Title | Aging and neurodegeneration are associated with increased mutations in single human neurons. |
Journal | Science |
Publication date | 2018.02 |
Disease | Cockayne syndrome Xeroderma Pigmentosum |
Number of cases | Male cases: 3; Female cases: 6; cases of unknown sex: 15; |