ATP synthase subunit O, mitochondrial is an enzyme that in humans is encoded by the ATP5PO gene.[5]

ATP5PO
Identifiers
AliasesATP5PO, ATPO, OSCP, HMC08D05, ATP synthase, H+ transporting, mitochondrial F1 complex, O subunit, ATP synthase peripheral stalk subunit OSCP, ATP5O
External IDsMGI: 106341 HomoloGene: 1283 GeneCards: ATP5PO
Gene location (Human)
Chromosome 21 (human)
Chr.Chromosome 21 (human)[1]
Chromosome 21 (human)
Genomic location for ATP5PO
Genomic location for ATP5PO
Band21q22.11Start33,903,453 bp[1]
End33,915,814 bp[1]
RNA expression pattern
PBB GE ATP5O 200818 at fs.png
More reference expression data
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001697

NM_138597

RefSeq (protein)

NP_001688

NP_613063

Location (UCSC)Chr 21: 33.9 – 33.92 MbChr 16: 91.93 – 91.93 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

The protein encoded by this gene is a component of the F-type ATPase found in the mitochondrial matrix. F-type ATPases are composed of a catalytic core and a membrane proton channel. The encoded protein appears to be part of the connector linking these two components and may be involved in transmission of conformational changes or proton conductance. [5]

ReferencesEdit

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000241837 - Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000022956 - Ensembl, May 2017
  3. ^ "Human PubMed Reference:".
  4. ^ "Mouse PubMed Reference:".
  5. ^ a b "Entrez Gene: ATP5PO ATP synthase peripheral stalk subunit OSCP".

External linksEdit

Further readingEdit