DRD2

GENERAL INFORMATION

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Gene name

DRD2

Gene description

Dopamine receptor D2

Protein class

Disease related genes
FDA approved drug targets
G-protein coupled receptors
Predicted intracellular proteins
Predicted membrane proteins

Predicted localization

Intracellular,Membrane

Number of transcripts

7
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Tissue enhanced (adrenal gland)
GTEx:Tissue enriched (salivary gland)

Protein evidence

Evidence at protein level

Protein localization

Distinct staining was observed in neuropil and processes in CNS. Lymphoid tissues displayed strong cytoplasmic staining. Gastrointestinal tract, endometrial glands and placental trophoblasts showed moderate membranous and cytoplasmic staining. Endothelial cells were distinctly stained. Remaining normal tissues were in general weakly stained or negative.

ANTIBODY RELIABILITY

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Data reliability
description

Pending RNA-based expert annotation.

Data reliability

Uncertain based on 1 antibody.
HPA015691
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RNA AND PROTEIN EXPRESSION SUMMARY

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RNA expression (FPKM) Protein expression (score)
Brain
Endocrine tissues
Bone marrow & immune system
Muscle tissues
Lung
Liver & gallbladder
Pancreas
Gastrointestinal tract
Kidney & urinary bladder
Male tissues
Female tissues
Adipose & soft tissue
Skin
Cerebral cortex

Hippocampus

Lymph node

Liver

Colon

Kidney

Testis



PROTEIN EXPRESSION OVERVIEW

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Organ

Expression



RNA EXPRESSION OVERVIEW

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HPA dataset
RNA tissue category:  Tissue enhanced (adrenal gland)

Organ

Expression

GTEx dataset
RNA tissue category:  Tissue enriched (salivary gland)

Organ

Expression



GENE INFORMATION

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Gene name

DRD2

Synonyms

Description

Dopamine receptor D2 (HGNC Symbol)

Entrez gene summary

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]

Chromosome

11

Cytoband

q23.2

Chromosome location (bp)

113409615 - 113475691

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000149295 (version 78.38)

Entrez gene

1813

UniProt

P14416 (UniProt - Evidence at protein level)

neXtProt

NX_P14416

Antibodypedia

DRD2 antibodies


PROTEIN BROWSER

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ENST00000346454
 
ENST00000362072
 
ENST00000538967
 
ENST00000542616
 
ENST00000542968
 
ENST00000543292
 
ENST00000544518
 
 
 
 


PROTEIN INFORMATION

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Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

DRD2-001 ENSP00000354859
ENST00000362072
P14416
Show all »
Show » Show » 443 50.6 No 7
DRD2-003 ENSP00000278597
ENST00000346454
P14416
Show all »
Show » Show » 414 47.3 No 7
DRD2-004 ENSP00000442172
ENST00000542968
P14416
Show all »
Show » Show » 443 50.6 No 7
DRD2-005 ENSP00000441068
ENST00000544518
F8VUV1
Show all »
Show » Show » 442 50.5 No 7
DRD2-006 ENSP00000441474
ENST00000542616
Show » 7 0.8 No 0
DRD2-007 ENSP00000438419
ENST00000543292
Q6LDH7
Show all »
Show » Show » 177 20.1 No 4
DRD2-010 ENSP00000438215
ENST00000538967
P14416
Show all »
Show » Show » 445 50.8 No 7