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Gene information for ATP5A1 (Homo sapiens)
(Information is obtained from NCBI Gene database)
Entrez gene ID498
Official gene symbolATP5A1
Full nameATP synthase, H+ transporting, mitochondrial F1 complex, alpha subunit 1, cardiac muscle
Aliases,ATP5A,ATP5AL2,ATPM,MOM2,OMR,ORM,hATP1,
Gene summaryThis gene encodes a subunit of mitochondrial ATP synthase. Mitochondrial ATP synthase catalyzes ATP synthesis, using 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 alpha subunit of the catalytic core. Alternatively spliced transcript variants encoding the same protein have been identified. Pseudogenes of this gene are located on chromosomes 9, 2, and 16. [provided by RefSeq]
LocationChromosome: 18   Locus: 18q12-q21
Gene position43684199 - 43664110  Map Viewer
Gene orientationminus
Gene size20090 bp
Gene sequence
OMIM ID164360