Gene
slc7a14b
- ID
- ZDB-GENE-091113-47
- Name
- solute carrier family 7 member 14b
- Symbol
- slc7a14b Nomenclature History
- Previous Names
-
- si:ch211-230g15.6
- Type
- protein_coding_gene
- Location
- Chr: 24 Mapping Details/Browsers
- Description
- Predicted to have transmembrane transporter activity. Predicted to be involved in transmembrane transport. Predicted to localize to integral component of membrane. Human ortholog(s) of this gene implicated in retinitis pigmentosa 68. Orthologous to human SLC7A14 (solute carrier family 7 member 14).
- 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 |
---|---|---|---|
retinitis pigmentosa 68 | Alliance | Retinitis pigmentosa 68 | 615725 |
Domain, Family, and Site Summary
Domain Details Per Protein
Protein | Length | Amino acid/polyamine transporter I | Cationic amino acid transporter, C-terminal |
---|---|---|---|
UniProtKB:E7F8S7
|
756 |
Type | Name | Annotation Method | Has Havana Data | Length (nt) | Analysis |
---|---|---|---|---|---|
mRNA |
slc7a14b-201
(1)
|
Ensembl | 2,271 nt |
Interactions and Pathways
No data available
Plasmids
No data available