Publication for ATP5ME and UQCRQ

Species Symbol Function* Entrez Gene ID* Other ID Gene
coexpression
CoexViewer
hsa ATP5ME ATP synthase membrane subunit e 521 [link]
hsa UQCRQ ubiquinol-cytochrome c reductase complex III subunit VII 27089

Pubmed ID Priority Text
26124562 0.98 ATP5I - ATP synthase H+ transporting mitochondrial F0 complex subunit E, ATP5J - ATP synthase H+ transporting mitochondrial F0 complex subunit F6, BAD - Bcl-2-associated death promoter, BAX - Bcl-2-associated x protein, Bcl-2 - B-cell lymphoma 2, BDNF - brain derived neurotrophic factor, COX5B - Cytochrome c oxidase subunit Vb, COX7A2 - cytochrome c oxidase subunit VIIa polypeptide 2, DLK - dual leucine zipper-bearing kinase, GABA - Gamma aminobutyric acid, IL-8 - Interleukin 8, NDUFA1 - NADH dehydrogenase 1 alpha subcomplex 1, NDUFB2 - NADH dehydrogenase1 beta subcomplex 2, NDUFS4 - NADH dehydrogenase Fe-S protein 4, NGF - nerve growth factor, PPP2R5C - protein phosphatase 2 regulatory subunit B gamma, PSMA3 - proteasome subunit alpha type 3, PSMA7 - proteasome subunit alpha type 7, PSMB1 - proteasome subunit beta type 1, PSMB6 - proteasome subunit beta type 6, PSMB7 - proteasome subunit beta type 7, PSMC2 - proteasome 26S subunit ATPase 2, PSMC5 - proteasome 26S subunit ATPase 5, SLC6A4 - solute carrier family 6 member 4, TNFa - tumor necrosis factor a, UBE2A - ubiquitinconjugating enzyme E2A, UCRC - ubiquinol-cytochrome c reductase complex, UFC1 - ubiquitin-fold modifier conjugating enzyme 1, UQCRQ - ubiquinol-cytochrome c reductase complex III subunit VII, USP14 - ubiquitin specific protease 14.
0.97 UQCRQ on BD_Brain and 9 genes such as UCRC, NDUFB2, ATP5I, NDUFA1, ATP5J on BD_Blood1 (Table 2A (see supplementary meterial)).
20528768 0.98 UQCRQ (ubiquinol-cytochrome c reductase, complex III subunit VII), COX7C (cytochrome c oxidase subunit VIIc), and ATP5I (ATP synthase, H+ transporting, mitochondrial F0 complex, subunit E) were greater in patients with CAD relative to control subjects.
30678683 0.98 Uqcrq, Uqcr11), ATP synthase complex (Atp5e, Atp5k), and ribosomal subunits (Rplp0, Rps25), some of which in humans have been implicated in schizophrenia and schizoaffective disorder.
29416685 0.89 UQCRQ), 14 genes for complex IV cytochrome c oxidase (COX4I1, COX4I2, COX5A, COX5B, COX6A1, COX6A2, COX6B1, COX6B2, COX6C, COX7A2, COX7A2L, COX7B, COX8A, and COX8C), and 25 genes for complex V ATP synthase (ATP12A, ATP4A, ATP4B, ATP5A1, ATP5B, ATP5C1, ATP5F1, ATP5G1, ATP5G2, ATP5G3, ATP5H, ATP5I, ATP5J, ATP5J2, ATP5L, ATP5O, ATP6V0A2, ATP6V0D2, ATP6V1C2, ATP6V1E2, ATP6V1G3, LHPP, OXA1L, PPA1, and PPA2) (Figure 4A).



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