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GENE - TERM ANNOTATION REPORT

RGD ID: 620091
Species: Rattus norvegicus
RGD Object: Gene
Symbol: Upb1
Name: beta-ureidopropionase 1
Acc ID: DOID:630
Term: genetic disease
Definition: A disease that has_material_basis_in genetic variations in the human genome. (DO)
Definition Source(s): http://ghr.nlm.nih.gov/ "DO" "DO"
Note: Use of the qualifier "multiple interactions" designates that the annotated interaction is comprised of a complex set of reactions and/or regulatory events, possibly involving additional chemicals and/or gene products.
Object SymbolQualifierEvidenceWithReferenceSourceNotesOriginal Reference(s)
Upb1 ISOUPB1 (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:11783491 PMID:15385443 PMID:16199547 PMID:17065070 PMID:22525402 PMID:24526388 PMID:25741868 PMID:25741913 PMID:28492532 PMID:30608453 PMID:35151535 PMID:35926322
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