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GENE - TERM ANNOTATION REPORT

4 Annotations Found.

An association has been curated linking Nrxn1 and autism spectrum disorder in Rattus norvegicus.        

  • The association was inferred from mutant phenotype (IMP)
  •  
  • The annotation was made from Esclassan F, etal., Behav Neurosci. 2015 Feb;129(1):74-85. doi: 10.1037/bne0000024. Epub 2014 Nov 24.
  • 19 additional annotations were made from Esclassan F, etal., Behav Neurosci. 2015 Feb;129(1):74-85. doi: 10.1037/bne0000024. Epub 2014 Nov 24.
  • 2362 RGD objects have been annotated to autism spectrum disorder  (DOID:0060041)
  • 31 papers in RGD have been used to annotate Nrxn1


  • An association has been curated linking Nrxn1 and autism spectrum disorder 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]
  • 2362 RGD objects have been annotated to autism spectrum disorder  (DOID:0060041)
  • 31 papers in RGD have been used to annotate Nrxn1
  • Curation Notes: CTD Direct Evidence: marker/mechanism
  • Original References(s): PMID:18252227


  • An association has been curated linking Nrxn1 and autism spectrum disorder in Rattus norvegicus.        

  • The association was inferred from sequence or structural similarity (ISS)
  •  
  • The annotation was made from RGD automated import pipeline for MGI gene-to-disease annotations
  • The annotation has been inferred from sequence or structural similarity with Nrxn1 (Mus musculus) [(IAGP) inferred by association of genotype and phenotype]
  • 2362 RGD objects have been annotated to autism spectrum disorder  (DOID:0060041)
  • 31 papers in RGD have been used to annotate Nrxn1


  • An association has been curated linking Nrxn1 and autism spectrum disorder 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]
  • 2362 RGD objects have been annotated to autism spectrum disorder  (DOID:0060041)
  • 31 papers in RGD have been used to annotate Nrxn1
  • Curation Notes: ClinVar Annotator: match by term: Autism spectrum disorder
  • Original References(s): PMID:19896112 PMID:21964664 PMID:23495017 PMID:23533028 PMID:25149956 PMID:25741868 PMID:27569545 PMID:28492532 PMID:30031152


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