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ATP5F1A gene

ATP synthase F1 subunit alpha

Key facts

Official symbol
ATP5F1A
Full name
ATP5F1A
Chromosome
18
Map location
18q21.1
Organism
Homo sapiens
NCBI Gene ID
498
Also known as
ATP5A, ATP5A1, ATP5AL2, ATPM, COXPD22, HEL-S-123m

Function summary

This 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 different isoforms have been identified. Pseudogenes of this gene are located on chromosomes 9, 2, and 16. [provided by RefSeq, Mar 2012].

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Data source: NCBI Gene · alsesAI Gene Library