Gene
slc38a8a
- ID
- ZDB-GENE-121005-5
- Name
- solute carrier family 38 member 8a
- Symbol
- slc38a8a Nomenclature History
- Previous Names
-
- slc38a8
- zmp:0000000533
- zmp:0000001044
- Type
- protein_coding_gene
- Location
- Chr: 18 Mapping Details/Browsers
- Description
- Predicted to localize to integral component of membrane. Orthologous to human SLC38A8 (solute carrier family 38 member 8).
- 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 |
|---|---|---|---|
| foveal hypoplasia 2 | Alliance | Foveal hypoplasia 2, with or without optic nerve misrouting and/or anterior segment dysgenesis | 609218 |
Domain, Family, and Site Summary
| Type | InterPro ID | Name |
|---|---|---|
| Domain | IPR013057 | Amino acid transporter, transmembrane domain |
Domain Details Per Protein
| Protein | Length | Amino acid transporter, transmembrane domain |
|---|---|---|
|
UniProtKB:A0A0G2KE96
|
||
|
UniProtKB:F1QK49
|
441 | |
|
UniProtKB:A5WVQ9
|
441 |
- Genome Browsers
Interactions and Pathways
No data available
Plasmids
No data available
- Comparative Orthology
- Alliance