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Gene : ATP5PD Homo sapiens

Name  ? ATP synthase peripheral stalk subunit d Cytological Location  17q25.1
Brief Description  ATP synthase peripheral stalk subunit d
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 seems to have nine subunits (a, b, c, d, e, f, g, F6 and 8). This gene encodes the d subunit of the Fo complex. Alternatively spliced transcript variants encoding different isoforms have been identified for this gene. In addition, three pseudogenes are located on chromosomes 9, 12 and 15. [provided by RefSeq, Jun 2010]
  • synonyms:
  • ATP5PD,
  • OTTHUMG00000179219,
  • ATPQ,
  • ATP synthase, H+ transporting, mitochondrial Fo complex, subunit d,
  • ATP5H,
  • NM_006356,
  • ATP5JD,
  • APT5H,
  • ATPQ,
  • uc002jmn.2,
  • ATP5H,
  • ATP synthase, H+ transporting, mitochondrial F0 complex, subunit d,
  • AF087135,
  • HGNC:845,
  • ATP synthase, H+ transporting, mitochondrial Fo complex subunit D
  • identifiers:
  • 10476,
  • ENSG00000167863,
  • ATP5PD

Genome feature

Region: gene ? Length: 8107  
Location: 17:75038863-75046969 reverse strand Cyto location: 17q25.1

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924 SN Ps

5 Cross References

16 Data Sets

8 Homologues

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97 Rna Seq Results