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 protein, plays a role in the inhibition of adenylyl cyclase activity. A missense mutation in this gene causes myoclonus dystonia and allelic variant mutants are associated with schizophrenia. (NCI Thesaurus)

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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…

DRD2 1 Allele

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

DRD1 wt Allele

Human DRD1 wild-type allele is located in the vicinity of 5q35.1 and is approximately 3 kb in length. This allele, which encodes…

DRD1 Gene

This gene is involved in the regulation of dopamine receptor transport and neuronal signal transduction pertaining to neuronal growth and development. …

Draw

Represent by making a drawing of, as with pencil, chalk, etc. on a surface; make a mark or lines on a…