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GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking Gabra5 and autistic disorder in Mus musculus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from Fatemi SH, etal., J Autism Dev Disord. 2010 Jun;40(6):743-50.
  • The annotation has been inferred from sequence orthology with GABRA5 (Homo sapiens) [(IEP) inferred from expression pattern]
  • 8 additional annotations were made from Fatemi SH, etal., J Autism Dev Disord. 2010 Jun;40(6):743-50.
  • 1912 RGD objects have been annotated to autistic disorder  (DOID:12849)
  • 10 papers in RGD have been used to annotate Gabra5


    • An association has been curated linking Gabra5 and autistic disorder in Mus musculus.        

  • 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 GABRA5 (Homo sapiens) [(EXP) inferred from experiment]
  • 1912 RGD objects have been annotated to autistic disorder  (DOID:12849)
  • 10 papers in RGD have been used to annotate Gabra5
  • Curation Notes: CTD Direct Evidence: marker/mechanism
  • Original References(s): PMID:17353214


    • An association has been curated linking Gabra5 and autistic disorder in Mus musculus.        

  • 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 GABRA5 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1912 RGD objects have been annotated to autistic disorder  (DOID:12849)
  • 10 papers in RGD have been used to annotate Gabra5
  • Curation Notes: ClinVar Annotator: match by term: Autism | ClinVar Annotator: match by term: Chromosome 15q11-q13 duplication syndrome
  • Original References(s): PMID:21681106 PMID:25741868 PMID:30208311 PMID:31690835


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