Gene
slc38a8b
- ID
- ZDB-GENE-121005-6
- Name
- solute carrier family 38 member 8b
- Symbol
- slc38a8b Nomenclature History
- Previous Names
- None
- Type
- protein_coding_gene
- Location
- Chr: 7 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:A0A8M9PPQ5
|
444 |
| Type | Name | Annotation Method | Has Havana Data | Length (nt) | Analysis |
|---|---|---|---|---|---|
| mRNA |
slc38a8b-201
(1)
|
Ensembl | 1,876 nt | ||
| mRNA |
slc38a8b-202
(1)
|
Ensembl | 1,932 nt |
Interactions and Pathways
No data available
Plasmids
No data available