COA3 - cytochrome c oxidase assembly factor 3 Gene
Also Known as COX25; hCOA3; CCDC56; HSPC009; MC4DN14; MITRAC12
Species: Homo sapiens
About COA3
This gene has 2 transcripts (splice variants), 194 orthologues and is associated with 2 phenotypes. Ubiquitous expression in kidney (RPKM 59.3), duodenum (RPKM 48.8) and 25 other tissues.
Summary
This gene encodes a member of the cytochrome c oxidase assembly factor family. Studies of a related gene in fly suggest that the encoded protein is localized to mitochondria and is essential for cytochrome c oxidase function. [provided by RefSeq, Nov 2012]
COA3 Products (1)
| mRNA | Protein | Name |
|---|---|---|
| NM_001040431.3 | NP_001035521.1 | cytochrome c oxidase assembly factor 3 homolog, mitochondrial |
| Molecular Function GO Annotation | Evidence | References | Source |
|---|---|---|---|
| enables protein binding |
IPI
IPI: Inferred from physical interaction
|
23260140 | GOA |
| Biological Process GO Annotation | Evidence | References | Source |
|---|---|---|---|
| involved in mitochondrial cytochrome c oxidase assembly |
IMP
IMP: Inferred from mutant phenotype
|
23260140 | GOA |
| involved in positive regulation of mitochondrial translation |
IMP
IMP: Inferred from mutant phenotype
|
23260140 | GOA |
| Cellular Component GO Annotation | Evidence | References | Source |
|---|---|---|---|
| located in mitochondrial inner membrane |
IDA
IDA: Inferred from direct assay
|
23260140 | GOA |
COA3 Protein Structure
Coiled-coil_56: Coiled-coil domain-containing protein 56 (11 - 104)
- 0
- 100
- 106 a.a.
| Protein Preferred Names | Protein Names | |
|---|---|---|
|
cytochrome c oxidase assembly factor 3 homolog, mitochondrial |
|
COA3 Protein-protein interaction Information
|
Type
|
Protein Name | Protein ID | Interactor | Interactor Species | Interactor ID | Detection Method | References |
|---|---|---|---|---|---|---|---|
|
Intra
|
COA3 | Q9Y2R0 | MT-CO1 | Homo sapiens | P00395 | 23260140 | |
|
Intra
|
COA3 | Q9Y2R0 | MT-CO1 | Homo sapiens | P00395 | 23260140 | |
|
Intra
|
COA3 | Q9Y2R0 | MT-CO1 | Homo sapiens | P00395 | 23260140 | |
|
Intra
|
COA3 | Q9Y2R0 | SURF1 | Homo sapiens | Q15526 | 23260140 | |
|
Intra
|
COA3 | Q9Y2R0 | SURF1 | Homo sapiens | Q15526 | 23260140 |
Related Diseases
| Diseases | Alias | |
|---|---|---|
| Mitochondrial Complex Iv Deficiency, Nuclear Type 14 |
|
|
| Isolated Cytochrome C Oxidase Deficiency |
|
|
| Mitochondrial Complex Iv Deficiency, Nuclear Type 1 |
|
|
| Demyelinating Polyneuropathy |
|
|
| Familial Isolated Hypoparathyroidism |
|
|
| Polyneuropathy |
|
|
| Myoclonic Epilepsy Associated With Ragged-Red Fibers |
|
|
| Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, And Stroke-Like Episodes |
|
|
| Leigh Syndrome |
|
|
Orthologs Information
| Species | Symbol | Source | ID |
|---|---|---|---|
| Felis catus | COA3 | VGNC | VGNC:61041 |
| Rattus norvegicus | COA3 | RGD | RGD:1564337 |
| Mus musculus | COA3 | MGD | MGI:1098757 |
| Bos taurus | COA3 | VGNC | VGNC:27543 |
| Others | COA3 | NCBI |