Homo sapiens Gene: COX7A1 | |||||||||
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Summary | |||||||||
InnateDB Gene | IDBG-46615.5 | ||||||||
Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||||
Gene Symbol | COX7A1 | ||||||||
Gene Name | cytochrome c oxidase subunit VIIa polypeptide 1 (muscle) | ||||||||
Synonyms | COX7A; COX7AH; COX7AM | ||||||||
Species | Homo sapiens | ||||||||
Ensembl Gene | ENSG00000161281 | ||||||||
Encoded Proteins |
cytochrome c oxidase subunit VIIa polypeptide 1 (muscle)
cytochrome c oxidase subunit VIIa polypeptide 1 (muscle)
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Protein Structure | |||||||||
Useful resources | Stemformatics EHFPI ImmGen | ||||||||
Entrez Gene | |||||||||
Summary |
Cytochrome c oxidase (COX), the terminal component of the mitochondrial respiratory chain, catalyzes the electron transfer from reduced cytochrome c to oxygen. This component is a heteromeric complex consisting of 3 catalytic subunits encoded by mitochondrial genes and multiple structural subunits encoded by nuclear genes. The mitochondrially-encoded subunits function in electron transfer, and the nuclear-encoded subunits may function in the regulation and assembly of the complex. This nuclear gene encodes polypeptide 1 (muscle isoform) of subunit VIIa and the polypeptide 1 is present only in muscle tissues. Other polypeptides of subunit VIIa are present in both muscle and nonmuscle tissues, and are encoded by different genes. [provided by RefSeq, Jul 2008] |
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Gene Information | |||||||||
Type | Protein coding | ||||||||
Genomic Location | Chromosome 19:36150922-36152869 | ||||||||
Strand | Reverse strand | ||||||||
Band | q13.12 | ||||||||
Transcripts |
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Interactions | |||||||||
Number of Interactions |
This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
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Gene Ontology | |||||||||
Molecular Function |
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Biological Process |
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Cellular Component |
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Orthologs | |||||||||
Species
Mus musculus
Bos taurus
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Gene ID
Gene Order
Not yet available
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Pathways | |||||||||
NETPATH | |||||||||
REACTOME | |||||||||
KEGG |
Alzheimer's disease pathway
Oxidative phosphorylation pathway
Parkinson's disease pathway
Huntington's disease pathway
Cardiac muscle contraction pathway
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INOH | |||||||||
PID NCI | |||||||||
Cross-References | |||||||||
SwissProt | |||||||||
TrEMBL | |||||||||
UniProt Splice Variant | |||||||||
Entrez Gene | |||||||||
UniGene | |||||||||
RefSeq | NM_001864 | ||||||||
HUGO | |||||||||
OMIM | |||||||||
CCDS | CCDS12490 | ||||||||
HPRD | 00481 | ||||||||
IMGT | |||||||||
EMBL | |||||||||
GenPept | |||||||||
RNA Seq Atlas | |||||||||