| Entrez gene ID | | 10476 |
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| Official gene symbol | | ATP5H |
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| Full name | | ATP synthase, H+ transporting, mitochondrial F0 complex, subunit d |
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| Aliases | | ,ATP5JD,ATPQ, |
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| Gene summary | | Mitochondrial ATP synthase catalyzes ATP synthesis, utilizing an electrochemical gradient of protons across the inner membrane during oxidative phosphorylation. It is composed of two linked multi-subunit complexes: the soluble catalytic core, F1, and the membrane-spanning component, Fo, which comprises the proton channel. The F1 complex consists of 5 different subunits (alpha, beta, gamma, delta, and epsilon) assembled in a ratio of 3 alpha, 3 beta, and a single representative of the other 3. The Fo seems to have nine subunits (a, b, c, d, e, f, g, F6 and 8). This gene encodes the d subunit of the Fo complex. Alternatively spliced transcript variants encoding different isoforms have been identified for this gene. In addition, three pseudogenes are located on chromosomes 9, 12 and 15. [provided by RefSeq] |
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| Location | | Chromosome: 17 Locus: 17q25 |
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| Gene position | | 73043074 - 73034955 Map Viewer |
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| Gene orientation | | minus |
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| Gene size | | 8120 bp |
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| Gene sequence |
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