Gene
slc25a26
- ID
- ZDB-GENE-050913-126
- Name
- solute carrier family 25 member 26
- Symbol
- slc25a26 Nomenclature History
- Previous Names
-
- SAMC (1)
- zgc:110080
- Type
- protein_coding_gene
- Location
- Chr: 11 Mapping Details/Browsers
- Description
- Predicted to have S-adenosyl-L-methionine transmembrane transporter activity. Predicted to localize to mitochondrial inner membrane. Human ortholog(s) of this gene implicated in combined oxidative phosphorylation deficiency 28. Orthologous to human SLC25A26 (solute carrier family 25 member 26).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 1 figure from Thisse et al., 2004
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
-
- MGC:110080 (1 image)
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 |
|---|---|---|---|
| combined oxidative phosphorylation deficiency 28 | Alliance | Combined oxidative phosphorylation deficiency 28 | 616794 |
Domain, Family, and Site Summary
Domain Details Per Protein
| Protein | Length | Mitochondrial carrier domain superfamily | Mitochondrial substrate/solute carrier |
|---|---|---|---|
|
UniProtKB:Q4V9P0
|
267 | ||
|
UniProtKB:B2GQ56
|
267 |
| Type | Name | Annotation Method | Has Havana Data | Length (nt) | Analysis |
|---|---|---|---|---|---|
| mRNA |
slc25a26-201
(1)
|
Ensembl | 1,311 nt | ||
| mRNA |
slc25a26-202
(1)
|
Ensembl | 870 nt |
Interactions and Pathways
No data available
Plasmids
No data available