MGP Database

New search | Record Overview | Ontology/Pathway Information | Domain Information | UniProt Annotations | Related Proteins
MGP006183

Ontology/Pathway Information

Entrez Gene ID84896
Gene NameATPase family, AAA domain containing 1
Gene Symbol ATAD1
SpeciesHomo sapiens
Gene Ontology (GO Annotations)
GO IDSourceTypeDescription
GO:0030054 IEA:UniProtKB-KWCcell junction
GO:0016020 IDA:UniProtKBCmembrane
GO:0005739 IEA:EnsemblCmitochondrion
GO:0005634 IBA:GO_CentralCnucleus
GO:0005778 IDA:UniProtKBCperoxisomal membrane
GO:0045211 ISS:UniProtKBCpostsynaptic membrane
GO:0016887 ISS:UniProtKBFATPase activity
GO:0005524 IEA:UniProtKB-KWFATP binding
GO:0008568 IBA:GO_CentralFmicrotubule-severing ATPase activity
GO:0006200 IBA:GOCPATP catabolic process
GO:0031122 IBA:GO_CentralPcytoplasmic microtubule organization
GO:0007612 ISS:UniProtKBPlearning
GO:0007613 ISS:UniProtKBPmemory
GO:0051967 ISS:UniProtKBPnegative regulation of synaptic transmission, glutamatergic
GO:0002092 ISS:UniProtKBPpositive regulation of receptor internalization
SMP Pathway Links
SMP IDDescription
SMP00535Adenine phosphoribosyltransferase deficiency (APRT)
SMP00144Adenosine Deaminase Deficiency
SMP00167Adenylosuccinate Lyase Deficiency
SMP00168AICA-Ribosiduria
SMP00427Azathioprine Action Pathway
SMP00365Gout or Kelley-Seegmiller Syndrome
SMP00364Lesch-Nyhan Syndrome (LNS)
SMP00428Mercaptopurine Action Pathway
SMP00536Mitochondrial DNA depletion syndrome
SMP00203Molybdenum Cofactor Deficiency
SMP00537Myoadenylate deaminase deficiency
SMP00050Purine Metabolism
SMP00210Purine Nucleoside Phosphorylase Deficiency
SMP00430Thioguanine Action Pathway
SMP00220Xanthine Dehydrogenase Deficiency (Xanthinuria)
SMP00512Xanthinuria type I
SMP00513Xanthinuria type II
  logo