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Gene information for ATP5J2 (Homo sapiens)
(Information is obtained from NCBI Gene database)
Entrez gene ID9551
Official gene symbolATP5J2
Full nameATP synthase, H+ transporting, mitochondrial F0 complex, subunit F2
Aliases,ATP5JL,
Gene summaryMitochondrial 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 catalytic portion of mitochondrial ATP synthase consists of five different subunits (alpha, beta, gamma, delta, and epsilon) assembled with a stoichiometry of 3 alpha, 3 beta, and single representatives of the gamma, delta, and epsilon subunits. The proton channel likely has nine subunits (a, b, c, d, e, f, g, F6 and 8). This gene encodes the f subunit of the Fo complex. Alternatively spliced transcript variants encoding different isoforms have been identified for this gene. This gene has multiple pseudogenes. Naturally occurring read-through transcription also exists between this gene and the downstream pentatricopeptide repeat domain 1 (PTCD1) gene. [provided by RefSeq]
LocationChromosome: 7   Locus: 7q22.1
Gene position99063808 - 99055784  Map Viewer
Gene orientationminus
Gene size8025 bp
Gene sequence