Sco2 - SCO2 cytochrome c oxidase assembly protein Gene
Species: Mus musculus
Summary
Predicted to enable protein-disulfide reductase activity. Acts upstream of or within several processes, including copper ion homeostasis; respiratory chain complex IV assembly; and response to activity. Located in mitochondrion. Is expressed in several structures, including alimentary system; aorta; blastocyst; gonad; and hemolymphoid system gland. Used to study cytochrome-c oxidase deficiency disease. Human ortholog(s) of this gene implicated in cytochrome-c oxidase deficiency disease; fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency 1; hypertrophic cardiomyopathy; and myopia. Orthologous to human SCO2 (synthesis of cytochrome C oxidase 2). [provided by Alliance of Genome Resources, Apr 2022]
Sco2 Products (1)
| mRNA | Protein | Name |
|---|---|---|
| NM_001111288.2 | NP_001104758.1 | protein SCO2 homolog, mitochondrial |
| Biological Process GO Annotation | Evidence | References | Source |
|---|---|---|---|
| acts upstream of or within copper ion homeostasis |
IMP
IMP: Inferred from mutant phenotype
|
19837698 | MGI |
| acts upstream of or within in utero embryonic development |
IMP
IMP: Inferred from mutant phenotype
|
19837698 | MGI |
| acts upstream of or within muscle system process |
IMP
IMP: Inferred from mutant phenotype
|
19837698 | MGI |
| acts upstream of or within respiratory chain complex IV assembly |
IMP
IMP: Inferred from mutant phenotype
|
19837698 | MGI |
| acts upstream of or within respiratory electron transport chain |
IMP
IMP: Inferred from mutant phenotype
|
19837698 | MGI |
| acts upstream of or within response to activity |
IMP
IMP: Inferred from mutant phenotype
|
19837698 | MGI |
| Cellular Component GO Annotation | Evidence | References | Source |
|---|---|---|---|
| located in mitochondrion |
IDA
IDA: Inferred from direct assay
|
19837698 | MGI |
| Protein Preferred Names | Protein Names | |
|---|---|---|
|
protein SCO2 homolog, mitochondrial |
|