Send us a Message
Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   
Search RGD Grant Resources Citing RGD About Us Contact Us
Genes Variants Community Projects QTLs Strains Markers Genome Information Ontologies Cell Lines References Download Submit Data
OntoMate (Literature Search) JBrowse (Genome Browser) Synteny Browser (VCMap) Variant Visualizer Multi-Ontology Enrichment (MOET) Gene-Ortholog Location Finder (GOLF) InterViewer (Protein-Protein Interactions) PhenoMiner (Quatitative Phenotypes) Gene Annotator OLGA (Gene List Generator) AllianceMine GViewer (Genome Viewer)
Aging & Age-Related Disease Cancer & Neoplastic Disease Cardiovascular Disease Coronavirus Disease Developmental Disease Diabetes Hematologic Disease Immune & Inflammatory Disease Infectious Disease Liver Disease Neurological Disease Obesity & Metabolic Syndrome Renal Disease Respiratory Disease Sensory Organ Disease
Find Models Genetic Models Autism Models Rat PhenoMiner (Quantitative Phenotypes) Chinchilla PhenoMiner Expected Ranges (Quantitative Phenotype) PhenoMiner Term Comparison Hybrid Rat Diversity Panel Phenotypes Phenotypes in Other Animal Models Animal Husbandry Strain Medical Records Phylogenetics Strain Availability Calendar Rats 101 Submissions Photo Archive
Pathways
Rat Community Forum Directory of Rat Laboratories Video Tutorials News RGD Publications RGD Presentations Archive Nomenclature Guidelines Resource Links Laboratory Resources Employment Resources
Advanced Search (OLGA)

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
go back to main search page
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


show annotations for term's descendants           Sort by:
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 chr13:96,865,634...96,893,506 JBrowse link
G Chst11 carbohydrate sulfotransferase 11 ISO SMPDB SMP:00532 NCBI chr 7:20,524,535...20,743,008 JBrowse link
G Papss2 3'-phosphoadenosine 5'-phosphosulfate synthase 2 ISO SMPDB SMP:00532 NCBI chr 1:239,867,597...239,952,614 JBrowse link
G Sult1a1 sulfotransferase family 1A member 1 ISO SMPDB SMP:00532 NCBI chr 1:190,702,592...190,706,112 JBrowse link
G Sult1e1 sulfotransferase family 1E member 1 ISO SMPDB SMP:00532 NCBI chr14:20,422,324...20,439,562 JBrowse link
G Sult2b1 sulfotransferase family 2B member 1 ISO SMPDB SMP:00532 NCBI chr 1:96,200,155...96,261,295 JBrowse link
G Suox sulfite oxidase ISO SMPDB SMP:00532 NCBI chr 7:1,687,666...1,691,759 JBrowse link
Term paths to the root
Path 1
Term Annotations click to browse term
  pathway 6091
    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
              sulfite oxidase deficiency pathway 7
paths to the root