Gene
slc25a10b
- ID
- ZDB-GENE-040426-1095
- Name
- solute carrier family 25 member 10b
- Symbol
- slc25a10b Nomenclature History
- Previous Names
-
- slc25a10
- zgc:56614 (1)
- Type
- protein_coding_gene
- Location
- Chr: 1 Mapping Details/Browsers
- Description
- Predicted to act upstream of or within mitochondrial transport. Predicted to be located in mitochondrial membrane. Is expressed in ovary. Human ortholog(s) of this gene implicated in mitochondrial DNA depletion syndrome. Orthologous to human SLC25A10 (solute carrier family 25 member 10).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 3 figures from 3 publications
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
-
- MGC:56614 (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 |
|---|---|---|---|
| mitochondrial DNA depletion syndrome 19 | Alliance | ?Mitochondrial DNA depletion syndrome 19 | 618972 |
Domain, Family, and Site Summary
Domain Details Per Protein
| Protein | Length | Mitochondrial carrier domain superfamily | Mitochondrial carrier protein | Mitochondrial Metabolite Transporter | Mitochondrial substrate/solute carrier |
|---|---|---|---|---|---|
|
UniProtKB:Q7ZWA7
|
286 |
- Genome Browsers
| Type | Name | Annotation Method | Has Havana Data | Length (nt) | Analysis |
|---|---|---|---|---|---|
| mRNA |
slc25a10b-201
(1)
|
Ensembl | 2,890 nt |
Interactions and Pathways
No data available
Plasmids
No data available