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GENE - TERM ANNOTATION REPORT

5 Annotations Found.

An association has been curated linking SCN1A and autistic disorder in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:8624395 (Homo sapiens)
  • 6255 RGD objects have been annotated to autistic disorder  (DOID:12849)
  • 8 papers in RGD have been used to annotate SCN1A
  • Curation Notes: ClinVar Annotator: match by term: Autistic disorder
  • Original References(s): PMID:12610651 PMID:28492532


    • An association has been curated linking SCN1A and autistic disorder in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:8624370 (Homo sapiens)
  • 6255 RGD objects have been annotated to autistic disorder  (DOID:12849)
  • 8 papers in RGD have been used to annotate SCN1A
  • Curation Notes: ClinVar Annotator: match by term: Autistic disorder
  • Original References(s): PMID:11254445 PMID:12610651 PMID:19200853 PMID:19522081 PMID:23195492 PMID:25741868 PMID:26990884 PMID:28492532 PMID:29358611


    • An association has been curated linking SCN1A and autistic disorder in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:8624341 (Homo sapiens)
  • 6255 RGD objects have been annotated to autistic disorder  (DOID:12849)
  • 8 papers in RGD have been used to annotate SCN1A
  • Curation Notes: ClinVar Annotator: match by term: Autistic disorder
  • Original References(s): PMID:14672992 PMID:17347258 PMID:28492532 PMID:32581362


    • An association has been curated linking SCN1A and autistic disorder in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:10048706 (Homo sapiens)
  • 6255 RGD objects have been annotated to autistic disorder  (DOID:12849)
  • 8 papers in RGD have been used to annotate SCN1A
  • Curation Notes: ClinVar Annotator: match by term: Autistic disorder
  • Original References(s): PMID:12566275 PMID:16199547 PMID:17347258 PMID:18930999 PMID:20522430 PMID:22071555 PMID:22409937 PMID:23934111 PMID:25741868 PMID:28148630 PMID:28492532 PMID:29190809 PMID:32581362


    • An association has been curated linking SCN1A and autistic disorder in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:8624395 (Homo sapiens)
  • 6255 RGD objects have been annotated to autistic disorder  (DOID:12849)
  • 8 papers in RGD have been used to annotate SCN1A
  • Curation Notes: ClinVar Annotator: match by term: Autistic disorder
  • Original References(s): PMID:12610651 PMID:25741868 PMID:28492532


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