Gene
drd5a
- ID
- ZDB-GENE-130522-2
- Name
- dopamine receptor D5a
- Symbol
- drd5a Nomenclature History
- Previous Names
-
- D1Ba (1)
- Type
- protein_coding_gene
- Location
- Chr: 14 Mapping Details/Browsers
- Description
- Human ortholog(s) of this gene implicated in attention deficit hyperactivity disorder and blepharospasm. Orthologous to human DRD5 (dopamine receptor D5).
- Genome Resources
-
- Alliance (1)
- Gene:100536970 (1)
- Note
- None
- Comparative Information
- All Expression Data
- 1 figure from Leggieri et al., 2022
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
- No data available
Wild Type Expression Summary
- All Phenotype Data
- No data available
- Cross-Species Comparison
- Alliance
Phenotype Summary
Mutations
Human Disease
Disease Ontology Term | Multi-Species Data | OMIM Term | OMIM Phenotype ID |
---|---|---|---|
attention deficit hyperactivity disorder | Alliance | {Attention deficit-hyperactivity disorder, susceptibility to} | 143465 |
{Blepharospasm, primary benign} | 606798 |
Domain, Family, and Site Summary
Domain Details Per Protein
Protein | Length | Dopamine D5 receptor | Dopamine receptor family | GPCR, rhodopsin-like, 7TM | G protein-coupled receptor, rhodopsin-like |
---|---|---|---|---|---|
UniProtKB:A0A8M1RJ11
|
281 |
- Genome Browsers
Interactions and Pathways
No data available
Plasmids
No data available
- Comparative Orthology
- Alliance