Gene
coa7
- ID
- ZDB-GENE-041014-16
- Name
- cytochrome c oxidase assembly factor 7
- Symbol
- coa7 Nomenclature History
- Previous Names
-
- selrc1
- si:ch211-11m18.2
- zgc:136252
- Type
- protein_coding_gene
- Location
- Chr: 20 Mapping Details/Browsers
- Description
- Predicted to be located in mitochondrion. Predicted to be active in mitochondrial intermembrane space. Human ortholog(s) of this gene implicated in spinocerebellar ataxia with axonal neuropathy type 3. Orthologous to human COA7 (cytochrome c oxidase assembly factor 7).
- 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 |
|---|---|---|---|
| spinocerebellar ataxia with axonal neuropathy type 3 | Alliance | Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 3 | 618387 |
Domain, Family, and Site Summary
Domain Details Per Protein
| Protein | Length | Beta-lactamase HcpB-like | Sel1-like repeat | Tetratricopeptide-like helical domain superfamily |
|---|---|---|---|---|
|
UniProtKB:Q5TYQ3
|
229 |
Interactions and Pathways
No data available
Plasmids
No data available