Gene
slc25a21
- ID
- ZDB-GENE-060929-664
- Name
- solute carrier family 25 member 21
- Symbol
- slc25a21 Nomenclature History
- Previous Names
-
- zgc:153387
- Type
- protein_coding_gene
- Location
- Chr: 17 Mapping Details/Browsers
- Description
- Predicted to have transmembrane transporter activity. Predicted to be involved in transmembrane transport. Predicted to localize to integral component of membrane. Human ortholog(s) of this gene implicated in mitochondrial DNA depletion syndrome. Orthologous to human SLC25A21 (solute carrier family 25 member 21).
- 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 |
|---|---|---|---|
| mitochondrial DNA depletion syndrome 18 | Alliance | ?Mitochondrial DNA depletion syndrome 18 | 618811 |
Domain, Family, and Site Summary
Domain Details Per Protein
| Protein | Length | Mitochondrial 2-oxodicarboxylate carrier | Mitochondrial carrier domain superfamily | Mitochondrial carrier protein | Mitochondrial substrate/solute carrier |
|---|---|---|---|---|---|
|
UniProtKB:Q08C83
|
298 |
| Type | Name | Annotation Method | Has Havana Data | Length (nt) | Analysis |
|---|---|---|---|---|---|
| mRNA |
slc25a21-201
(1)
|
Ensembl | 1,954 nt |
Interactions and Pathways
No data available
Plasmids
No data available