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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: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 Anpep alanyl aminopeptidase, membrane ISO SMPDB SMP:00501 NCBI chr 1:143,176,645...143,219,447 JBrowse link
G Casp7 caspase 7 ISO SMPDB SMP:00501 NCBI chr 1:265,442,647...265,481,938 JBrowse link
G Gclc glutamate-cysteine ligase, catalytic subunit ISO SMPDB SMP:00501 NCBI chr 8:87,510,251...87,548,896 JBrowse link
G Gclm glutamate cysteine ligase, modifier subunit ISO SMPDB SMP:00501 NCBI chr 2:213,032,135...213,052,192 JBrowse link
G Ggct gamma-glutamyl cyclotransferase ISO SMPDB SMP:00501 NCBI chr 4:85,453,387...85,459,597 JBrowse link
G Ggt6 gamma-glutamyl transferase 6 ISO SMPDB SMP:00501 NCBI chr10:57,550,447...57,553,461 JBrowse link
G Gpx1 glutathione peroxidase 1 ISO SMPDB SMP:00501 NCBI chr 8:117,905,462...117,906,588 JBrowse link
G Gsr glutathione-disulfide reductase ISO SMPDB SMP:00501 NCBI chr16:65,185,574...65,228,742 JBrowse link
G Gss glutathione synthetase ISO SMPDB SMP:00501 NCBI chr 3:164,508,005...164,538,343 JBrowse link
G Gsto2 glutathione S-transferase omega 2 ISO SMPDB SMP:00501 NCBI chr 1:256,673,376...256,695,154 JBrowse link
G Oplah 5-oxoprolinase (ATP-hydrolysing) ISO SMPDB SMP:00501 NCBI chr 7:109,892,136...109,932,403 JBrowse link
Term paths to the root
Path 1
Term Annotations click to browse term
  pathway 6092
    disease pathway 1954
      congenital disease pathway 530
        inborn genetic disease pathway 530
          inborn error of metabolism pathway 530
            inborn error of amino acid metabolism pathway 229
              glutathionuria disease pathway 11
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