DRD5 wt Allele

Human DRD5 wild-type allele is located in the vicinity of 4p16.1 and is approximately 2 kb in length. This allele, which encodes D(1B) dopamine receptor protein, plays a role in the stimulation of adenylate cyclase activity and intracellular accumulation of cAMP. Defects in DRD5 are a cause of blepharospasm, a primary focal dystonia affecting the orbicularis oculi muscles. (NCI Thesaurus)

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DRD5 Gene

This gene plays a regulatory role in adenylate cyclase activity and intracellular cAMP store accumulation. The gene is thought to act as…

DRD4 wt Allele

Human DRD4 wild-type allele is located in the vicinity of 11p15.5 and is approximately 3 kb in length. This allele, which encodes…

DRD4 Gene

This gene plays a role in G protein-coupled receptor signal transduction and inhibits adenylyl cyclase activity.

DRD2 wt Allele

Human DRD2 wild-type allele is located within 11q23 and is approximately 66 kb in length. This allele, which encodes D(2) dopamine receptor…

DRD2 Gene

This gene plays an inhibitory role in the regulation of adenylyl cyclase activity.

DRD2 2 Allele

Human DRD2 Gene at 11q23 encodes Dopamine Receptor D2, a G-protein coupled receptor that inhibits adenylyl cyclase activity. Missense mutation in DRD2…