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GENE - TERM ANNOTATION REPORT

RGD ID: 1308190
Species: Rattus norvegicus
RGD Object: Gene
Symbol: Cul3
Name: cullin 3
Acc ID: DOID:9004952
Term: NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT AUTISM OR SEIZURES
Definition: This is a disease characterized by global developmental delay apparent in infancy, impaired intellectual development, and speech delay.
Definition Source(s): OMIM:619239
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)
Cul3 ISOCUL3 (Homo sapiens)7240710OMIM  
Cul3 ISOCUL3 (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Neurodevelopmental disorder with or without autism or seizuresPMID:16199547 PMID:25741868 PMID:27824329 PMID:28492532 PMID:29361671 PMID:32341456 PMID:32860008 PMID:33004838
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