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GENE - TERM ANNOTATION REPORT

4 Annotations Found.

An association has been curated linking Nlgn3 and autism spectrum disorder in Rattus norvegicus.        

  • The association was inferred from mutant phenotype (IMP)
    		•  
  • The annotation was made from Thomas AM, etal., Sleep. 2017 Oct 1;40(10). pii: 4100612. doi: 10.1093/sleep/zsx138.
  • 36 additional annotations were made from Thomas AM, etal., Sleep. 2017 Oct 1;40(10). pii: 4100612. doi: 10.1093/sleep/zsx138.
  • 2359 RGD objects have been annotated to autism spectrum disorder  (DOID:0060041)
  • 19 papers in RGD have been used to annotate Nlgn3


    • An association has been curated linking Nlgn3 and autism spectrum disorder in Rattus norvegicus.        

  • The association was inferred from mutant phenotype (IMP)
    		•  
  • The annotation was made from Hamilton SM, etal., Behav Neurosci. 2014 Apr;128(2):103-9. doi: 10.1037/a0035988.
  • 43 additional annotations were made from Hamilton SM, etal., Behav Neurosci. 2014 Apr;128(2):103-9. doi: 10.1037/a0035988.
  • 2359 RGD objects have been annotated to autism spectrum disorder  (DOID:0060041)
  • 19 papers in RGD have been used to annotate Nlgn3


    • An association has been curated linking Nlgn3 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 Nlgn3 (Mus musculus) [(IAGP) inferred by association of genotype and phenotype]
  • 2359 RGD objects have been annotated to autism spectrum disorder  (DOID:0060041)
  • 19 papers in RGD have been used to annotate Nlgn3


    • An association has been curated linking Nlgn3 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 NLGN3 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2359 RGD objects have been annotated to autism spectrum disorder  (DOID:0060041)
  • 19 papers in RGD have been used to annotate Nlgn3
  • Curation Notes: ClinVar Annotator: match by term: Autism spectrum disorder
  • Original References(s): PMID:25741868


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