ATP6
protein-coding gene in the species Homo sapiens
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Summary
ATP6 is a gene[1]. ATP6 ranks in the top 2% of gene entities by monthly Wikipedia readership (126 views/month).[2]
Key Facts
- Subclass of: protein-coding gene[3]
- HomoloGene ID: 5012[4]
- Genomic start: 8527[5]
- Genomic end: 9207[6]
- Ortholog: ATP6[7]
- Encodes: ATP synthase F0 subunit 6[8]
- Found in taxon: Homo sapiens[9]
- Chromosome: human mitochondrial DNA[10]
- Genetic association: neuropathy, ataxia, and retinitis pigmentosa[11], Leber hereditary optic neuropathy[12]
- Strand orientation: forward strand[13]
- Exact match: http://identifiers.org/ncbigene/4508[14]
- Expressed in: left uterine tube[15], gastric mucosa[16], Descending thoracic aorta[17], right hemisphere of cerebellum[18], body of uterus[19], mucosa of transverse colon[20], prostate[21], right ovary[22], right lung[23], muscle layer of sigmoid colon[24]
Why It Matters
ATP6 is known by 5 alternative names across languages and contexts.[25]