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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:sulfite oxidase deficiency pathway
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Accession:PW:0001647 term browser browse the term
Definition:An autosomal recessive inherited condition resulting from alteration in sulfur metabolism. It exhibits severe neurological symptoms in the neonatal period and is possibly fatal.
Synonyms:exact_synonym: isolated sulfite oxidase deficiency pathway;   sulfocysteinuria pathway
 related_synonym: SMP:00532


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sulfite oxidase deficiency pathway term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Bpnt1 3'(2'), 5'-bisphosphate nucleotidase 1 ISO SMPDB SMP:00532 NCBI chr13:103,268,045...103,292,848
Ensembl chr13:103,268,068...103,292,854
JBrowse link
G Chst11 carbohydrate sulfotransferase 11 ISO SMPDB SMP:00532 NCBI chr 7:26,641,856...26,890,503
Ensembl chr 7:26,645,422...26,859,716
JBrowse link
G Papss2 3'-phosphoadenosine 5'-phosphosulfate synthase 2 ISO SMPDB SMP:00532 NCBI chr 1:251,145,264...251,230,716
Ensembl chr 1:251,145,253...251,230,715
JBrowse link
G Sult1a1 sulfotransferase family 1A member 1 ISO SMPDB SMP:00532 NCBI chr 1:198,100,586...198,104,106
Ensembl chr 1:198,100,586...198,104,109
JBrowse link
G Sult1e1 sulfotransferase family 1E member 1 ISO SMPDB SMP:00532 NCBI chr14:22,070,861...22,089,264
Ensembl chr14:22,072,024...22,089,248
JBrowse link
G Sult2b1 sulfotransferase family 2B member 1 ISO SMPDB SMP:00532 NCBI chr 1:101,712,254...101,774,683
Ensembl chr 1:101,710,959...101,773,508
JBrowse link
G Suox sulfite oxidase ISO SMPDB SMP:00532 NCBI chr 7:3,098,228...3,102,179
Ensembl chr 7:3,098,245...3,102,142
JBrowse link

Term paths to the root
Path 1
Term Annotations click to browse term
  pathway 6103
    disease pathway 1957
      congenital disease pathway 529
        inborn genetic disease pathway 529
          inborn error of metabolism pathway 529
            inborn error of amino acid metabolism pathway 229
              sulfite oxidase deficiency pathway 7
paths to the root