| Gene Symbol |
SCO1
|
| Entrez Gene |
6341
|
| Alt Symbol |
SCOD1
|
| Species |
Human
|
| Gene Type |
protein-coding
|
| Description |
SCO1 cytochrome c oxidase assembly protein
|
| Other Description |
SCO cytochrome oxidase deficient homolog 1|protein SCO1 homolog, mitochondrial
|
| Swissprots |
O75880 B2RDM0
|
| Accessions |
AAG23836 EAW89997 O75880 AF026852 AAD08641 AF131816 AAD20051 AF183424 AAG09693 AK074588 BAG51973 AK098826 AK315595 BAG37967 BC015504 AAH15504 BM981070 BM994602 DA571370 DQ891605 ABM82531 DQ894798 ABM85724 XM_005256751 XP_005256808 NM_004589 NP_004580
|
| Function |
Thought to play a role in cellular copper homeostasis, mitochondrial redox signaling or insertion of copper into the active site of COX. {ECO:0000269|PubMed:15659396, ECO:0000269|PubMed:16735468, ECO:0000269|PubMed:17189203}.
|
| Subcellular Location |
Mitochondrion {ECO:0000269|PubMed:9878253}.
|
| Tissue Specificity |
Predominantly expressed in tissues characterized by high rates of oxidative phosphorylation (OxPhos), including muscle, heart, and brain. {ECO:0000269|PubMed:9878253}.
|