Gene

coa8

ID
ZDB-GENE-090313-66
Name
cytochrome c oxidase assembly factor 8
Symbol
coa8 Nomenclature History
Previous Names
  • apopt1
  • si:ch211-194h13.2 (1)
Type
protein_coding_gene
Location
Chr: 13 Mapping Details/Browsers
Description
Predicted to be involved in intrinsic apoptotic signaling pathway. Predicted to localize to mitochondrion. Human ortholog(s) of this gene implicated in cytochrome-c oxidase deficiency disease. Orthologous to human COA8 (cytochrome c oxidase assembly factor 8).
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
No data available
Cross-Species Comparison
Alliance
Phenotype Summary
Mutations
Mutants
Sequence Targeting Reagents
Human Disease
Associated With coa8 Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
mitochondrial complex IV deficiency nuclear type 17 Alliance Mitochondrial complex IV deficiency, nuclear type 17 619061
Associated With coa8 Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Family IPR018796 Cytochrome c oxidase assembly factor 8
Domain Details Per Protein
Protein Length Cytochrome c oxidase assembly factor 8
UniProtKB:B8A5M9 205
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