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GENE - TERM ANNOTATION REPORT

RGD ID: 619978
Species: Rattus norvegicus
RGD Object: Gene
Symbol: Csnk2b
Name: casein kinase 2 beta
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)
Csnk2b ISOCSNK2B (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:25741868 PMID:28492532 PMID:33166063 PMID:33644862 PMID:34041744
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