DRD2 Chromosome 11
Dopamine receptor D2
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What This Gene Does
This gene encodes the D2 subtype of the dopamine receptor. This G-protein coupled receptor inhibits adenylyl cyclase activity. A missense mutation in this gene causes myoclonus dystonia; other mutations have been associated with schizophrenia. Alternative splicing of this gene results in two transcript variants encoding different isoforms. A third variant has been described, but it has not been determined whether this form is normal or due to aberrant splicing. [provided by RefSeq, Jul 2008]
Gene Info
Gene Group
"Dopamine receptors|MicroRNA protein coding host genes"
Locus Type
gene with protein product
Location
11q23.2
Ensembl
ENSG00000149295
Associated Conditions (2)
Dystonic disorder
DRD2-associated Dystonia
Key Variants
RS138873192
Conflicting classifications of pathogenicity
Dystonic disorder, Dystonic disorder
Health Risk
RS1800496
Conflicting classifications of pathogenicity
Dystonic disorder, DRD2-associated Dystonia, Dystonic disorder
Health Risk
RS201137518
Conflicting classifications of pathogenicity
Dystonic disorder, Dystonic disorder
Health Risk
RS747312255
Conflicting classifications of pathogenicity
Dystonic disorder, Dystonic disorder
Health Risk
All Variants (4)
| RSID | Category | Clinical Significance | Conditions |
|---|---|---|---|
| RS138873192 | Health Risk | Conflicting classifications of pathogenicity | Dystonic disorder, Dystonic disorder |
| RS1800496 | Health Risk | Conflicting classifications of pathogenicity | Dystonic disorder, DRD2-associated Dystonia, Dystonic disorder |
| RS201137518 | Health Risk | Conflicting classifications of pathogenicity | Dystonic disorder, Dystonic disorder |
| RS747312255 | Health Risk | Conflicting classifications of pathogenicity | Dystonic disorder, Dystonic disorder |