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
Expression
All Expression Data
No data available
Cross-Species Comparison
High Throughput Data
Thisse Expression Data
No data available
Wild Type Expression Summary
Phenotype
All Phenotype Data
2 figures from 2 publications
Cross-Species Comparison
Alliance
Phenotype Summary
Mutations
Mutants
Sequence Targeting Reagents
Human Disease
Associated With coa6 Human Ortholog
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
Associated With coa6 Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Family IPR003213 Cytochrome c oxidase, subunit VIb
Family IPR042289 Cytochrome c oxidase assembly factor 6 homolog
Homologous_superfamily IPR036549 Cytochrome c oxidase, subunit VIb superfamily
Domain Details Per Protein
Protein Length Cytochrome c oxidase assembly factor 6 homolog Cytochrome c oxidase, subunit VIb Cytochrome c oxidase, subunit VIb superfamily
UniProtKB:B8A5J2 79
Transcripts
Genome Browsers
Interactions and Pathways
No data available
Antibodies
No data available
Plasmids
No data available
Constructs
Marker Relationships
Sequences
Orthology
Comparative Orthology
Alliance
Gene Tree
Ensembl
Citations