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Gene information for ATP5L (Homo sapiens)
(Information is obtained from NCBI Gene database)
Entrez gene ID10632
Official gene symbolATP5L
Full nameATP synthase, H+ transporting, mitochondrial F0 complex, subunit G
Aliases,ATP5JG,
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 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 g subunit of the Fo complex. Alternative splicing results in multiple transcript variants.
LocationChromosome: 11   Locus: 11q23.3
Gene position118272104 - 118280562  Map Viewer
Gene orientationplus
Gene size8459 bp
Gene sequence