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
- None
- 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