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GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking Nrxn1 and CHROMOSOME 2p16.3 DELETION SYNDROME in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • The annotation has been inferred from sequence orthology with NRXN1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to CHROMOSOME 2p16.3 DELETION SYNDROME  (DOID:9001388)
  • 31 papers in RGD have been used to annotate Nrxn1


    • An association has been curated linking Nrxn1 and CHROMOSOME 2p16.3 DELETION SYNDROME in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with NRXN1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to CHROMOSOME 2p16.3 DELETION SYNDROME  (DOID:9001388)
  • 31 papers in RGD have been used to annotate Nrxn1
  • Curation Notes: ClinVar Annotator: match by term: Chromosome 2p16.3 deletion syndrome
  • Original References(s): PMID:18179900 PMID:18945720 PMID:21681106 PMID:23495017 PMID:25741868 PMID:28492532


    • An association has been curated linking Nrxn1 and CHROMOSOME 2p16.3 DELETION SYNDROME in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from RGD automated import pipeline for CTD gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with NRXN1 (Homo sapiens) [(EXP) inferred from experiment]
  • 1 RGD objects have been annotated to CHROMOSOME 2p16.3 DELETION SYNDROME  (DOID:9001388)
  • 31 papers in RGD have been used to annotate Nrxn1
  • Curation Notes: CTD Direct Evidence: marker/mechanism


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