Gene
sco2
- ID
- ZDB-GENE-041210-173
- Name
- synthesis of cytochrome C oxidase 2
- Symbol
- sco2 Nomenclature History
- Previous Names
-
- si:dkey-202b22.3
- Type
- protein_coding_gene
- Location
- Chr: 4 Mapping Details/Browsers
- Description
- Predicted to enable protein-disulfide reductase activity. Predicted to be involved in eye development and mitochondrial cytochrome c oxidase assembly. Predicted to act upstream of or within intracellular copper ion homeostasis. Predicted to be located in mitochondrial inner membrane. Human ortholog(s) of this gene implicated in cytochrome-c oxidase deficiency disease; hypertrophic cardiomyopathy; mitochondrial complex IV deficiency nuclear type 2; and myopia. Orthologous to human SCO2 (synthesis of cytochrome C oxidase 2).
- 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
Domain, Family, and Site Summary
Domain Details Per Protein
Protein | Additional Resources | Length | Copper chaperone SCO1/SenC | Synthesis of cytochrome c oxidase, Sco1/Sco2 | Thioredoxin-like superfamily |
---|---|---|---|---|---|
UniProtKB:Q5RH02 | InterPro | 279 |
Interactions and Pathways
No data available
Plasmids
No data available