COX2
protein-coding gene in the species Homo sapiens
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Summary
COX2 is a gene[1]. COX2 is known by 7 alternative names across languages and contexts.[2]
Key Facts
- Subclass of: protein-coding gene[3]
- HomoloGene ID: 5017[4]
- Genomic start: 7586[5]
- Genomic end: 8269[6]
- Ortholog: COX2[7]
- Encodes: Cytochrome c oxidase subunit II[8]
- Found in taxon: Homo sapiens[9]
- Chromosome: human mitochondrial DNA[10]
- Genetic association: cytochrome-c oxidase deficiency disease[11]
- Strand orientation: forward strand[12]
- Exact match: http://identifiers.org/ncbigene/4513[13]
- Expressed in: mucosa of transverse colon[14], putamen[15], caudate nucleus[16], right frontal lobe[17], nucleus accumbens[18], right hemisphere of cerebellum[19], hippocampus proper[20], substantia nigra[21], muscle layer of sigmoid colon[22], hypothalamus[23]