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Gene information for ATP5C1 (Homo sapiens)
(Information is obtained from NCBI Gene database)
Entrez gene ID509
Official gene symbolATP5C1
Full nameATP synthase, H+ transporting, mitochondrial F1 complex, gamma polypeptide 1
Aliases,ATP5C,ATP5CL1,
Gene summaryThis gene encodes a subunit of mitochondrial ATP synthase. Mitochondrial ATP synthase catalyzes ATP synthesis, utilizing an electrochemical gradient of protons across the inner membrane during oxidative phosphorylation. ATP synthase is composed of two linked multi-subunit complexes: the soluble catalytic core, F1, and the membrane-spanning component, Fo, comprising the proton channel. The catalytic portion of mitochondrial ATP synthase consists of 5 different subunits (alpha, beta, gamma, delta, and epsilon) assembled with a stoichiometry of 3 alpha, 3 beta, and a single representative of the other 3. The proton channel consists of three main subunits (a, b, c). This gene encodes the gamma subunit of the catalytic core. Alternatively spliced transcript variants encoding different isoforms have been identified. This gene also has a pseudogene on chromosome 14. [provided by RefSeq]
LocationChromosome: 10   Locus: 10p15.1
Gene position7830093 - 7849764  Map Viewer
Gene orientationplus
Gene size19672 bp
Gene sequence
OMIM ID108729