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Gene : ATP5PF Homo sapiens
Name  ? ATP synthase peripheral stalk subunit F6 Cytological Location  21q21.3
Brief Description  ATP synthase peripheral stalk subunit F6
Description  Mitochondrial 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 complex has nine subunits (a, b, c, d, e, f, g, F6 and 8). This gene encodes the F6 subunit of the Fo complex. The F6 subunit is required for F1 and Fo interactions. Alternatively spliced transcript variants encoding different isoforms have been identified for this gene. This gene has 1 or more pseudogenes. [provided by RefSeq, Feb 2016]
  • synonyms:
  • uc002yls.4,
  • ATP5A,
  • ATP synthase, H+ transporting, mitochondrial Fo complex subunit F6,
  • ATP synthase, H+ transporting, mitochondrial F0 complex, subunit F6,
  • NM_001685,
  • ATP5J,
  • ATP5J,
  • coupling factor 6,
  • OTTHUMG00000078442,
  • ATPM,
  • F6,
  • ATP5PF,
  • ATPM,
  • ATP5A,
  • CF6,
  • M37104,
  • ATP synthase, H+ transporting, mitochondrial Fo complex, subunit F6,
  • ATP synthase subunit h,
  • HGNC:847,
  • CF6,
  • ATP5,
  • ATP5
  • identifiers:
  • 522,
  • ENSG00000154723,
  • ATP5PF

Genome feature

Region: gene ? Length: 11154  
Location: 21:25724500-25735653 reverse strand Cyto location: 21q21.3


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