Gene
slc25a15a
- ID
- ZDB-GENE-070112-1072
- Name
- solute carrier family 25 member 15a
- Symbol
- slc25a15a Nomenclature History
- Previous Names
-
- zgc:158707
- Type
- protein_coding_gene
- Location
- Chr: 15 Mapping Details/Browsers
- Description
- Predicted to have L-ornithine transmembrane transporter activity. Predicted to be involved in mitochondrial L-ornithine transmembrane transport. Predicted to localize to integral component of membrane. Human ortholog(s) of this gene implicated in amino acid metabolic disorder; citrullinemia; and ornithine translocase deficiency. Orthologous to human SLC25A15 (solute carrier family 25 member 15).
- 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 |
|---|---|---|---|
| ornithine translocase deficiency | Alliance | Hyperornithinemia-hyperammonemia-homocitrullinemia syndrome | 238970 |
Domain, Family, and Site Summary
Domain Details Per Protein
| Protein | Length | Mitochondrial Carrier | Mitochondrial carrier domain superfamily | Mitochondrial substrate/solute carrier |
|---|---|---|---|---|
|
UniProtKB:A1L288
|
303 |
- Genome Browsers
Interactions and Pathways
No data available
Plasmids
No data available