Gene

sco1

ID
ZDB-GENE-140909-1
Name
synthesis of cytochrome C oxidase 1
Symbol
sco1 Nomenclature History
Previous Names
None
Type
protein_coding_gene
Location
Chr: 3 Mapping Details/Browsers
Description
Predicted to enable metal ion binding activity. Predicted to be involved in mitochondrial cytochrome c oxidase assembly. Human ortholog(s) of this gene implicated in cytochrome-c oxidase deficiency disease and mitochondrial complex IV deficiency nuclear type 4. Orthologous to human SCO1 (synthesis of cytochrome C oxidase 1).
Genome Resources
Note
None
Comparative Information
Expression
All Expression Data
1 figure from Sun et al., 2019
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
Allele Type Localization Consequence Mutagen Supplier
sa8760Allele with one point mutationUnknownUnknownENU
1 - 1 of 1
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Sequence Targeting Reagents
Human Disease
Associated With sco1 Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
mitochondrial complex IV deficiency nuclear type 4 Alliance Mitochondrial complex IV deficiency, nuclear type 4 619048
1 - 1 of 1
Associated With sco1 Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Family IPR003782 Copper chaperone SCO1/SenC
Homologous_superfamily IPR036249 Thioredoxin-like superfamily
1 - 2 of 2
Domain Details Per Protein
Protein Additional Resources Length Copper chaperone SCO1/SenC Thioredoxin-like superfamily
UniProtKB:E7FD19 InterPro 318
1 - 1 of 1
Transcripts
Genome Browsers
Type Name Annotation Method Has Havana Data Length (nt) Analysis
mRNA sco1-201 (1) Ensembl 1,178 nt
1 - 1 of 1
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