Gene
slc7a14a
- ID
- ZDB-GENE-070912-112
- Name
- solute carrier family 7 member 14a
- Symbol
- slc7a14a Nomenclature History
- Previous Names
-
- si:ch211-152d1.2
- Type
- protein_coding_gene
- Location
- Chr: 2 Mapping Details/Browsers
- Description
- Predicted to have transmembrane transporter activity. Involved in eye development. Predicted to localize to integral component of membrane and lysosomal 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
- 1 figure from Zhuang et al., 2019
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
- No data available
Wild Type Expression Summary
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:B0UYF2
|
785 |
| Type | Name | Annotation Method | Has Havana Data | Length (nt) | Analysis |
|---|---|---|---|---|---|
| mRNA |
slc7a14a-201
(1)
|
Ensembl | 5,140 nt | ||
| mRNA |
slc7a14a-202
(1)
|
Ensembl | 458 nt | ||
| mRNA |
slc7a14a-203
(1)
|
Ensembl | 2,827 nt | ||
| mRNA |
slc7a14a-204
(1)
|
Ensembl | 3,085 nt |
Interactions and Pathways
No data available
Plasmids
No data available