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Gene : DRD2 Homo sapiens

Name  ? dopamine receptor D2 Cytological Location  11q23.2
Brief Description  dopamine receptor D2
Description  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]
  • synonyms:
  • D2R,
  • DRD2,
  • uc001poa.5,
  • HGNC:3023,
  • D2DR,
  • OTTHUMG00000167717,
  • M29066,
  • NM_000795
  • identifiers:
  • 1813,
  • ENSG00000149295,
  • DRD2

Genome feature

Region: gene ? Length: 65804  
Location: 11:113409595-113475398 reverse strand Cyto location: 11q23.2

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0 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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3753 SN Ps

5 Cross References

18 Data Sets

8 Homologues

0 Located Features

97 Rna Seq Results