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GENE - TERM ANNOTATION REPORT

RGD ID: 1315846
Species: Homo sapiens
RGD Object: Gene
Symbol: RAD51D
Name: RAD51 paralog D
Acc ID: DOID:0070271
Term: Lynch syndrome 1
Definition: A Lynch syndrome that has_material_basis_in heterozygous mutations in the MSH2 gene on chromosome 2p21-p16. (DO)
Definition Source(s): https://www.ncbi.nlm.nih.gov/pubmed/8261515 "DO" "DO", https://www.ncbi.nlm.nih.gov/pubmed/8574961 "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)
RAD51D IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Lynch syndrome 1PMID:21822267 PMID:25741868 PMID:26261251 PMID:26467025 PMID:28492532 PMID:29371908 PMID:31159747 PMID:33471991 PMID:34284872
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