Gene
coa6
- ID
- ZDB-GENE-070705-152
- Name
- cytochrome c oxidase assembly factor 6
- Symbol
- coa6 Nomenclature History
- Previous Names
-
- si:ch211-258f14.5
- Type
- protein_coding_gene
- Location
- Chr: 4 Mapping Details/Browsers
- Description
- Involved in heart development. Predicted to localize to mitochondrion. Human ortholog(s) of this gene implicated in fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency 4. Orthologous to human COA6 (cytochrome c oxidase assembly factor 6).
- 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
Phenotype Summary
Mutations
Human Disease
| Disease Ontology Term | Multi-Species Data | OMIM Term | OMIM Phenotype ID |
|---|---|---|---|
| mitochondrial complex IV deficiency nuclear type 13 | Alliance | Mitochondrial complex IV deficiency, nuclear type 13 | 616501 |
Domain, Family, and Site Summary
Domain Details Per Protein
| Protein | Length | Cytochrome c oxidase assembly factor 6 homolog | Cytochrome c oxidase subunit 6B/Cytochrome c oxidase assembly factor 6-like superfamily | Cytochrome oxidase c subunit VIb-like |
|---|---|---|---|---|
|
UniProtKB:B8A5J2
|
79 |
Interactions and Pathways
No data available
Plasmids
No data available