GABRA1 Chromosome 5
Gamma-aminobutyric acid type A receptor subunit alpha1
Upload your DNA to see your personal genotypes for variants in GABRA1.
What This Gene Does
This gene encodes a gamma-aminobutyric acid (GABA) receptor. 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. GABA-A receptors are pentameric, consisting of proteins from several subunit classes: alpha, beta, gamma, delta and rho. Mutations in this gene cause juvenile myoclonic epilepsy and childhood absence epilepsy type 4. Multiple transcript variants encoding the same protein have been identified for this gene. [provided by RefSeq, Jul 2008]
Gene Info
Gene Group
Gamma-aminobutyric acid type A receptor subunits
Locus Type
gene with protein product
Location
5q34
Ensembl
ENSG00000022355
Associated Conditions (14)
Epilepsy
idiopathic generalized
susceptibility to
13
childhood absence 4
Idiopathic generalized epilepsy
Developmental and epileptic encephalopathy
19
GABRA1-related disorder
Inborn genetic diseases
Intellectual disability
Epileptic encephalopathy
Juvenile myoclonic epilepsy
Intractable seizure
Key Variants
RS1064795283
Conflicting classifications of pathogenicity
Epilepsy, idiopathic generalized, susceptibility to
Health Risk
RS1064796448
Conflicting classifications of pathogenicity
Epilepsy, idiopathic generalized, susceptibility to
Health Risk
RS113886269
Conflicting classifications of pathogenicity
Epilepsy, idiopathic generalized, susceptibility to
Health Risk
RS1312078830
Conflicting classifications of pathogenicity
GABRA1-related disorder, Inborn genetic diseases, GABRA1-related disorder
Health Risk
RS1313965409
Conflicting classifications of pathogenicity
Idiopathic generalized epilepsy, Epilepsy, idiopathic generalized
Health Risk
RS138259457
Conflicting classifications of pathogenicity
Epilepsy, idiopathic generalized, susceptibility to
Health Risk
RS138671319
Conflicting classifications of pathogenicity
Epilepsy, idiopathic generalized, susceptibility to
Health Risk
RS139163545
Conflicting classifications of pathogenicity
Idiopathic generalized epilepsy, Epilepsy, idiopathic generalized
Health Risk
RS139793542
Conflicting classifications of pathogenicity
Epilepsy, idiopathic generalized, susceptibility to
Health Risk
RS142385746
Conflicting classifications of pathogenicity
Epilepsy, idiopathic generalized, susceptibility to
Health Risk
RS143815396
Conflicting classifications of pathogenicity
Epilepsy, idiopathic generalized, susceptibility to
Health Risk
RS144727170
Conflicting classifications of pathogenicity
Epilepsy, idiopathic generalized, susceptibility to
Health Risk
All Variants (127)
| RSID | Category | Clinical Significance | Conditions |
|---|---|---|---|
| RS1064795283 | Health Risk | Conflicting classifications of pathogenicity | Epilepsy, idiopathic generalized, susceptibility to |
| RS1064796448 | Health Risk | Conflicting classifications of pathogenicity | Epilepsy, idiopathic generalized, susceptibility to |
| RS113886269 | Health Risk | Conflicting classifications of pathogenicity | Epilepsy, idiopathic generalized, susceptibility to |
| RS1312078830 | Health Risk | Conflicting classifications of pathogenicity | GABRA1-related disorder, Inborn genetic diseases, GABRA1-related disorder |
| RS1313965409 | Health Risk | Conflicting classifications of pathogenicity | Idiopathic generalized epilepsy, Epilepsy, idiopathic generalized |
| RS138259457 | Health Risk | Conflicting classifications of pathogenicity | Epilepsy, idiopathic generalized, susceptibility to |
| RS138671319 | Health Risk | Conflicting classifications of pathogenicity | Epilepsy, idiopathic generalized, susceptibility to |
| RS139163545 | Health Risk | Conflicting classifications of pathogenicity | Idiopathic generalized epilepsy, Epilepsy, idiopathic generalized |
| RS139793542 | Health Risk | Conflicting classifications of pathogenicity | Epilepsy, idiopathic generalized, susceptibility to |
| RS142385746 | Health Risk | Conflicting classifications of pathogenicity | Epilepsy, idiopathic generalized, susceptibility to |
| RS143815396 | Health Risk | Conflicting classifications of pathogenicity | Epilepsy, idiopathic generalized, susceptibility to |
| RS144727170 | Health Risk | Conflicting classifications of pathogenicity | Epilepsy, idiopathic generalized, susceptibility to |
| RS1457242041 | Health Risk | Conflicting classifications of pathogenicity | Inborn genetic diseases, Inborn genetic diseases |
| RS1554087620 | Health Risk | Conflicting classifications of pathogenicity | Idiopathic generalized epilepsy, Epilepsy, idiopathic generalized |
| RS1561587910 | Health Risk | Conflicting classifications of pathogenicity | Epilepsy, idiopathic generalized, susceptibility to |
| RS1581175017 | Health Risk | Conflicting classifications of pathogenicity | Idiopathic generalized epilepsy, Epilepsy, idiopathic generalized |
| RS1581220210 | Health Risk | Conflicting classifications of pathogenicity | Epilepsy, idiopathic generalized, susceptibility to |
| RS1754197638 | Health Risk | Conflicting classifications of pathogenicity | Idiopathic generalized epilepsy, Epilepsy, idiopathic generalized |
| RS1754199170 | Health Risk | Conflicting classifications of pathogenicity | Idiopathic generalized epilepsy, Epilepsy, idiopathic generalized |
| RS1755063375 | Health Risk | Conflicting classifications of pathogenicity | Inborn genetic diseases, Developmental and epileptic encephalopathy, 19 |
| RS1755333582 | Health Risk | Conflicting classifications of pathogenicity | Idiopathic generalized epilepsy, Epilepsy, idiopathic generalized |
| RS1755340949 | Health Risk | Conflicting classifications of pathogenicity | Idiopathic generalized epilepsy, Epilepsy, idiopathic generalized |
| RS1755409878 | Health Risk | Conflicting classifications of pathogenicity | Idiopathic generalized epilepsy, Epilepsy, idiopathic generalized |
| RS182930988 | Health Risk | Conflicting classifications of pathogenicity | Epilepsy, idiopathic generalized, susceptibility to |
| RS183280626 | Health Risk | Conflicting classifications of pathogenicity | Developmental and epileptic encephalopathy, 19, Developmental and epileptic encephalopathy |
| RS184629690 | Health Risk | Conflicting classifications of pathogenicity | Epilepsy, idiopathic generalized, susceptibility to |
| RS187522588 | Health Risk | Conflicting classifications of pathogenicity | Epilepsy, idiopathic generalized, susceptibility to |
| RS188133840 | Health Risk | Conflicting classifications of pathogenicity | Idiopathic generalized epilepsy, Epilepsy, idiopathic generalized |
| RS190024862 | Health Risk | Conflicting classifications of pathogenicity | Epilepsy, idiopathic generalized, susceptibility to |
| RS190043578 | Health Risk | Conflicting classifications of pathogenicity | Epilepsy, idiopathic generalized, susceptibility to |
| RS200218956 | Health Risk | Conflicting classifications of pathogenicity | Idiopathic generalized epilepsy, Epilepsy, childhood absence 4 |
| RS200750234 | Health Risk | Conflicting classifications of pathogenicity | Epilepsy, idiopathic generalized, susceptibility to |
| RS2113354062 | Health Risk | Conflicting classifications of pathogenicity | Idiopathic generalized epilepsy, Epilepsy, idiopathic generalized |
| RS2113381632 | Health Risk | Conflicting classifications of pathogenicity | — |
| RS2113381723 | Health Risk | Conflicting classifications of pathogenicity | Epilepsy, idiopathic generalized, susceptibility to |
| RS2532205020 | Health Risk | Conflicting classifications of pathogenicity | Inborn genetic diseases, Inborn genetic diseases |
| RS2532205137 | Health Risk | Conflicting classifications of pathogenicity | Developmental and epileptic encephalopathy, 19, Epilepsy |
| RS2532239153 | Health Risk | Conflicting classifications of pathogenicity | — |
| RS2532261795 | Health Risk | Conflicting classifications of pathogenicity | Idiopathic generalized epilepsy, Epilepsy, idiopathic generalized |
| RS2532280401 | Health Risk | Conflicting classifications of pathogenicity | Epilepsy, idiopathic generalized, susceptibility to |
| RS372742479 | Health Risk | Conflicting classifications of pathogenicity | Epilepsy, idiopathic generalized, susceptibility to |
| RS374616425 | Health Risk | Conflicting classifications of pathogenicity | Epilepsy, idiopathic generalized, susceptibility to |
| RS376693195 | Health Risk | Conflicting classifications of pathogenicity | Idiopathic generalized epilepsy, Epilepsy, childhood absence 4 |
| RS41303356 | Health Risk | Conflicting classifications of pathogenicity | Epilepsy, idiopathic generalized, susceptibility to |
| RS41308303 | Health Risk | Conflicting classifications of pathogenicity | Epilepsy, idiopathic generalized, susceptibility to |
| RS527890421 | Health Risk | Conflicting classifications of pathogenicity | — |
| RS541335259 | Health Risk | Conflicting classifications of pathogenicity | Epilepsy, idiopathic generalized, susceptibility to |
| RS543710675 | Health Risk | Conflicting classifications of pathogenicity | Epilepsy, idiopathic generalized, susceptibility to |
| RS551045474 | Health Risk | Conflicting classifications of pathogenicity | Epilepsy, idiopathic generalized, susceptibility to |
| RS564871157 | Health Risk | Conflicting classifications of pathogenicity | Epilepsy, idiopathic generalized, susceptibility to |