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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 (

Term:glutathionuria disease pathway
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Accession:PW:0002562 term browser browse the term
Definition:An inherited condition resulting from alterations in glutathione metabolism.
Synonyms:exact_synonym: gamma-glutamyltransferase deficiency pathway;   gamma-glutamyltranspeptidase deficiency pathway
 related_synonym: SMP:00501

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glutathionuria disease pathway term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Casp7 caspase 7 ISO SMPDB SMP:00501 NCBI chrNW_004936486:4,082,664...4,114,942 JBrowse link
G Gclc glutamate-cysteine ligase catalytic subunit ISO SMPDB SMP:00501 NCBI chrNW_004936476:7,371,270...7,418,756 JBrowse link
G Ggct gamma-glutamylcyclotransferase ISO SMPDB SMP:00501 NCBI chrNW_004936478:6,786,392...6,794,088 JBrowse link
G Ggt6 gamma-glutamyltransferase 6 ISO SMPDB SMP:00501 NCBI chrNW_004936677:1,111,203...1,115,131 JBrowse link
G Gpx1 glutathione peroxidase 1 ISO SMPDB SMP:00501 NCBI chrNW_004936529:997,943...999,123 JBrowse link
G Gsr glutathione-disulfide reductase ISO SMPDB SMP:00501 NCBI chrNW_004936792:531,076...579,083 JBrowse link
G Gss glutathione synthetase ISO SMPDB SMP:00501 NCBI chrNW_004936561:5,765,637...5,793,951 JBrowse link
G Gsto2 glutathione S-transferase omega 2 ISO SMPDB SMP:00501 NCBI chrNW_004936600:1,907,396...1,925,256 JBrowse link
G LOC101972738 alanyl aminopeptidase, membrane ISO SMPDB SMP:00501 NCBI chrNW_004936483:15,563,540...15,582,521 JBrowse link
G LOC101977655 glutamate--cysteine ligase regulatory subunit ISO SMPDB SMP:00501 NCBI chrNW_004936537:5,356,914...5,378,998 JBrowse link
G Oplah 5-oxoprolinase, ATP-hydrolysing ISO SMPDB SMP:00501 NCBI chrNW_004936470:8,126,677...8,139,556 JBrowse link

Term paths to the root
Path 1
Term Annotations click to browse term
  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
              glutathionuria disease pathway 11
paths to the root