Variant ID | 22366 |
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Entrez Gene ID | 2556 |
Gene | GABRA3 (GeneCards) |
Location | hg19 X:151491587-151491587
hg38 X:152323115-152323115 |
Disease | Xeroderma Pigmentosum (view all the variants in this disease) |
Method | HiSeq X Ten |
Mutation(HGVS format) | NC_000023.10:g.151491587 T>C (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 | 155270560 |
MAF in gnomAD genome (version 2.0.1) | 0 |
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CADD Raw score (version 1.3) | -0.098609 (Deleterious) |
FATHMM raw prediction score | 0.06559 (Tolerated) |
Deleterious probability by DeFine | 0.0941 (Neutral) |
Entrez Gene ID | 2556 (NCBI Gene) |
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Official Gene Symbol | GABRA3 (GeneCards) |
Number of variants in GABRA3 in this database | 3 (view all the variants) |
Full name | gamma-aminobutyric acid type A receptor alpha3 subunit |
Band | Xq28 |
Other IDs | Vega: OTTHUMG00000024183 OMIM: 305660 HGNC: HGNC:4077 Ensembl: ENSG00000011677 |
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. [provided by RefSeq, Jul 2008] |
Individual ID | 29217584.23 (view all the variants in this individual) |
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Pubmed ID | 29217584 |
Whose mosaic mutation | Female Patient |
Phenotype | 3 |
Disease | Xeroderma Pigmentosum (view all the variants in this disease) |
OMIM ID | 278700 |
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; |