CKDdb-logoCKDdb - Molecule ID A0383

geneATP5F1
nameATP synthase B chain
speciesHomo sapiens

Molecule reference

SwissProtUniProtEnsEMBLGeneIDUniGeneOMIM
AT5F1_HUMANP24539ENSG00000116459515Hs.514870603270

Functions and classifications

GOC:mitochondrial matrix, C:mitochondrial proton-transporting ATP synthase complex, coupling factor F(o), F:proton-transporting ATP synthase activity, rotational mechanism, P:mitochondrial ATP synthesis coupled proton transport, P:respiratory electron transport chain, C:mitochondrial proton-transporting ATP synthase complex, coupling factor F(o), F:hydrogen ion transmembrane transporter activity, P:ATP synthesis coupled proton transport, F:hydrogen ion transporting ATP synthase activity, rotational mechanism, P:ATP catabolic process
UniProtAcetylation, CF(0), Complete proteome, Hydrogen ion transport, Ion transport, Membrane, Mitochondrion, Mitochondrion inner membrane, Polymorphism, Reference proteome, Transit peptide, Transport
PADBtransport, storage, endocytosis, exocytosis, vesicles

Studies, tissues and diseases

Study IDSpeciesNTissue / SourceCompartmentDiseaseFold change in diseaseP-valueDetectionPubMed/DOI
Exp19099603cMus musculus6kidneywholePolycystic_Kidney_Disease (Autosomal Dominant Polycystic kidney disease)0.480cDNA microarray19099603
Exp19099603dMus musculus6kidneywholePolycystic_Kidney_Disease (Autosomal Dominant Polycystic kidney disease)0.350cDNA microarray19099603
Exp19698090bHomo sapiens25bloodmononuclear cellsDialysis (hemodialysis)3.242.06E-09RNA microarray19698090

Compile date 08-10-2018© iMODE-CKD consortium