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PATHWAY ONTOLOGY - ANNOTATIONS

The Pathway Ontology (PW), is currently being developed at the Rat Genome Database. For more information about this vocabulary, please see Petri et al. The rat genome database pathway portal. Database (Oxford). 2011 Apr 8;2011:bar010. Print 2011 or contact us (http://rgd.mcw.edu/contact/index.shtml).

Term:GABA aminotransferase deficiency pathway
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Accession:PW:0002095 term browser browse the term
Definition:A condition caused by alterations in gamma aminobutyric acid metabolism due to defects in the 4-aminobutyrate aminotransferase enzyme.
Synonyms:exact_synonym: gamma aminobutyric acid transaminase deficiency pathway
 related_synonym: GABA transaminase deficiency pathway;   SMP:00351


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GABA aminotransferase deficiency pathway term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Abat 4-aminobutyrate aminotransferase ISO SMPDB SMP:00351 NCBI chrNW_004936530:7,543,743...7,621,392 JBrowse link
G Aldh2 aldehyde dehydrogenase 2 family member ISO SMPDB SMP:00351 NCBI chrNW_004936558:4,362,693...4,387,705 JBrowse link
G Aldh6a1 aldehyde dehydrogenase 6 family member A1 ISO SMPDB SMP:00351 NCBI chrNW_004936488:3,320,357...3,340,463 JBrowse link
G Cndp1 carnosine dipeptidase 1 ISO SMPDB SMP:00351 NCBI chrNW_004936616:3,955,847...3,984,021 JBrowse link
G Dpyd dihydropyrimidine dehydrogenase ISO SMPDB SMP:00351 NCBI chrNW_004936537:1,660,461...2,439,305 JBrowse link
G Dpys dihydropyrimidinase ISO SMPDB SMP:00351 NCBI chrNW_004936470:39,564,431...39,637,394 JBrowse link
G Gad1 glutamate decarboxylase 1 ISO SMPDB SMP:00351 NCBI chrNW_004936509:1,160,559...1,201,037 JBrowse link
G LOC101973421 amine oxidase copper containing 3 ISO SMPDB SMP:00351 NCBI chrNW_004936490:17,549,836...17,564,867 JBrowse link
G Upb1 beta-ureidopropionase 1 ISO SMPDB SMP:00351 NCBI chrNW_004936619:668,380...713,720 JBrowse link

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Path 1
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  pathway 3946
    disease pathway 686
      congenital disease pathway 506
        inborn genetic disease pathway 506
          inborn error of metabolism pathway 506
            inborn error of amino acid metabolism pathway 221
              GABA aminotransferase deficiency pathway 9
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