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GENE - TERM ANNOTATION REPORT

RGD ID: 628659
Species: Rattus norvegicus
RGD Object: Gene
Symbol: Nrxn1
Name: neurexin 1
Acc ID: DOID:9001388
Term: CHROMOSOME 2p16.3 DELETION SYNDROME
Definition: null
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)
Nrxn1susceptibilityISONRXN1 (Homo sapiens)7240710OMIM  
Nrxn1 ISONRXN1 (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Chromosome 2P16.3 deletion syndrome | ClinVar Annotator: match by term: Chromosome 2p16.3 deletion syndromePMID:18179900 PMID:18945720 PMID:21681106 PMID:23495017 PMID:25741868 PMID:28492532
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