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GENE - TERM ANNOTATION REPORT

RGD ID: 12551382
Species: Ictidomys tridecemlineatus
RGD Object: Gene
Symbol: Ctnnb1
Name: catenin beta 1
Acc ID: DOID:0111349
Term: hereditary desmoid disease
Definition: A syndrome characterized by extraintestinal manifestation of familial adenomatous polyposis that has_material_basis_in in some cases by extreme 3' mutation in APC on 5q22.2. (DO)
Definition Source(s): https://www.ncbi.nlm.nih.gov/pubmed/10782927 "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)
Ctnnb1 ISOCTNNB1 (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Desmoid tumor caused by somatic mutationPMID:10398436 PMID:10435629 PMID:10655994 PMID:25741868 PMID:26619011 PMID:26822237 PMID:9500465 PMID:9927029
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