Gene
slc1a3a
- ID
- ZDB-GENE-030131-2159
- Name
- solute carrier family 1 member 3a
- Symbol
- slc1a3a Nomenclature History
- Previous Names
- Type
- protein_coding_gene
- Location
- Chr: 5 Mapping Details/Browsers
- Description
- Predicted to have symporter activity. Predicted to localize to integral component of membrane. Human ortholog(s) of this gene implicated in episodic ataxia type 6. Is expressed in several structures, including glioblast; liver; nervous system; neural tube; and radial glial cell. Orthologous to human SLC1A3 (solute carrier family 1 member 3).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 24 figures from 16 publications
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
-
- IMAGE:7138008 (10 images)
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 |
|---|---|---|---|
| episodic ataxia type 6 | Alliance | Episodic ataxia, type 6 | 612656 |
Domain, Family, and Site Summary
Domain Details Per Protein
| Protein | Length | Dicarboxylate/Amino Acid:Cation Symporter | Sodium:dicarboxylate symporter | Sodium:dicarboxylate symporter, conserved site | Sodium:dicarboxylate symporter superfamily |
|---|---|---|---|---|---|
|
UniProtKB:Q6P4V2
|
537 |
- Genome Browsers
Interactions and Pathways
No data available
Plasmids
No data available