Gene
slc5a7b
- ID
- ZDB-GENE-140429-1
- Name
- solute carrier family 5 member 7b
- Symbol
- slc5a7b Nomenclature History
- Previous Names
- Type
- protein_coding_gene
- Location
- Unmapped
- Description
- Predicted to enable choline:sodium symporter activity. Predicted to be involved in acetylcholine biosynthetic process; chemical synaptic transmission; and choline transport. Predicted to act upstream of or within sodium ion transport and transmembrane transport. Predicted to be located in presynaptic membrane. Predicted to be active in several cellular components, including axon; dendrite; and perikaryon.
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- No data available
- 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 |
|---|---|---|---|
| autosomal dominant distal hereditary motor neuronopathy 7 | Alliance | Neuronopathy, distal hereditary motor, autosomal dominant 7 | 158580 |
| congenital myasthenic syndrome 20 | Alliance | Myasthenic syndrome, congenital, 20, presynaptic | 617143 |
Domain, Family, and Site Summary
Domain Details Per Protein
| Protein | Additional Resources | Length | High-affinity choline transporter | Sodium/glucose symporter superfamily | Sodium/solute symporter |
|---|---|---|---|---|---|
| UniProtKB:A0A8M1PUR8 | InterPro | 622 |
- Genome Browsers
- No data available
Interactions and Pathways
No data available
Plasmids
No data available
- Comparative Orthology
- Alliance