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GENE - TERM ANNOTATION REPORT

10 Annotations Found.

An association has been curated linking CUL3 and NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT AUTISM OR SEIZURES in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • 1 RGD objects have been annotated to NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT AUTISM OR SEIZURES  (DOID:9004952)
  • 10 papers in RGD have been used to annotate CUL3


    • An association has been curated linking CUL3 and NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT AUTISM OR SEIZURES 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:243049712 (Homo sapiens)
  • 1 RGD objects have been annotated to NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT AUTISM OR SEIZURES  (DOID:9004952)
  • 10 papers in RGD have been used to annotate CUL3
  • Curation Notes: ClinVar Annotator: match by term: Neurodevelopmental disorder with or without autism or seizures
  • Original References(s): PMID:25741868 PMID:32341456


    • An association has been curated linking CUL3 and NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT AUTISM OR SEIZURES 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:151759712 (Homo sapiens)
  • 1 RGD objects have been annotated to NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT AUTISM OR SEIZURES  (DOID:9004952)
  • 10 papers in RGD have been used to annotate CUL3
  • Curation Notes: ClinVar Annotator: match by term: Neurodevelopmental disorder with or without autism or seizures
  • Original References(s): PMID:16199547 PMID:25741868 PMID:27824329 PMID:28492532 PMID:32341456


    • An association has been curated linking CUL3 and NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT AUTISM OR SEIZURES 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:38597478 (Homo sapiens)
  • 1 RGD objects have been annotated to NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT AUTISM OR SEIZURES  (DOID:9004952)
  • 10 papers in RGD have been used to annotate CUL3
  • Curation Notes: ClinVar Annotator: match by term: Neurodevelopmental disorder with or without autism or seizures
  • Original References(s): PMID:25741868 PMID:32341456 PMID:32860008


    • An association has been curated linking CUL3 and NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT AUTISM OR SEIZURES 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:155798686 (Homo sapiens)
  • 1 RGD objects have been annotated to NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT AUTISM OR SEIZURES  (DOID:9004952)
  • 10 papers in RGD have been used to annotate CUL3
  • Curation Notes: ClinVar Annotator: match by term: Neurodevelopmental disorder with or without autism or seizures
  • Original References(s): PMID:25741868 PMID:28492532 PMID:32341456 PMID:33004838


    • An association has been curated linking CUL3 and NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT AUTISM OR SEIZURES 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:152978395 (Homo sapiens)
  • 1 RGD objects have been annotated to NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT AUTISM OR SEIZURES  (DOID:9004952)
  • 10 papers in RGD have been used to annotate CUL3
  • Curation Notes: ClinVar Annotator: match by term: Neurodevelopmental disorder with or without autism or seizures
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking CUL3 and NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT AUTISM OR SEIZURES 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:155796624|RGD:407429575 (Homo sapiens) & RGD:155796624|RGD:407429575 (Homo sapiens)
  • 1 RGD objects have been annotated to NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT AUTISM OR SEIZURES  (DOID:9004952)
  • 10 papers in RGD have been used to annotate CUL3
  • Curation Notes: ClinVar Annotator: match by term: Neurodevelopmental disorder with or without autism or seizures
  • Original References(s): PMID:25741868 PMID:29361671


    • An association has been curated linking CUL3 and NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT AUTISM OR SEIZURES 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:156227909 (Homo sapiens)
  • 1 RGD objects have been annotated to NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT AUTISM OR SEIZURES  (DOID:9004952)
  • 10 papers in RGD have been used to annotate CUL3
  • Curation Notes: ClinVar Annotator: match by term: Neurodevelopmental disorder with or without autism or seizures
  • Original References(s): PMID:28492532


    • An association has been curated linking CUL3 and NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT AUTISM OR SEIZURES 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:155794729|RGD:329351417 (Homo sapiens) & RGD:155794729|RGD:329351417 (Homo sapiens)
  • 1 RGD objects have been annotated to NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT AUTISM OR SEIZURES  (DOID:9004952)
  • 10 papers in RGD have been used to annotate CUL3
  • Curation Notes: ClinVar Annotator: match by term: Neurodevelopmental disorder with or without autism or seizures


    • An association has been curated linking CUL3 and NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT AUTISM OR SEIZURES 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:13832035|RGD:150435519|RGD:150495221|RGD:155642370|RGD:155642983|RGD:401721443|RGD:405706778|RGD:405710024|RGD:405855429|RGD:405866752|RGD:407573553 (Homo sapiens) & RGD:13832035|RGD:150435519|RGD:150495221|RGD:155642370|RGD:155642983|RGD:401721443|RGD:405706778|RGD:405710024|RGD:405855429|RGD:405866752|RGD:407573553 (Homo sapiens) & RGD:13832035|RGD:150435519|RGD:150495221|RGD:155642370|RGD:155642983|RGD:401721443|RGD:405706778|RGD:405710024|RGD:405855429|RGD:405866752|RGD:407573553 (Homo sapiens) & RGD:13832035|RGD:150435519|RGD:150495221|RGD:155642370|RGD:155642983|RGD:401721443|RGD:405706778|RGD:405710024|RGD:405855429|RGD:405866752|RGD:407573553 (Homo sapiens) & RGD:13832035|RGD:150435519|RGD:150495221|RGD:155642370|RGD:155642983|RGD:401721443|RGD:405706778|RGD:405710024|RGD:405855429|RGD:405866752|RGD:407573553 (Homo sapiens) & RGD:13832035|RGD:150435519|RGD:150495221|RGD:155642370|RGD:155642983|RGD:401721443|RGD:405706778|RGD:405710024|RGD:405855429|RGD:405866752|RGD:407573553 (Homo sapiens) & RGD:13832035|RGD:150435519|RGD:150495221|RGD:155642370|RGD:155642983|RGD:401721443|RGD:405706778|RGD:405710024|RGD:405855429|RGD:405866752|RGD:407573553 (Homo sapiens) & RGD:13832035|RGD:150435519|RGD:150495221|RGD:155642370|RGD:155642983|RGD:401721443|RGD:405706778|RGD:405710024|RGD:405855429|RGD:405866752|RGD:407573553 (Homo sapiens) & RGD:13832035|RGD:150435519|RGD:150495221|RGD:155642370|RGD:155642983|RGD:401721443|RGD:405706778|RGD:405710024|RGD:405855429|RGD:405866752|RGD:407573553 (Homo sapiens) & RGD:13832035|RGD:150435519|RGD:150495221|RGD:155642370|RGD:155642983|RGD:401721443|RGD:405706778|RGD:405710024|RGD:405855429|RGD:405866752|RGD:407573553 (Homo sapiens) & RGD:13832035|RGD:150435519|RGD:150495221|RGD:155642370|RGD:155642983|RGD:401721443|RGD:405706778|RGD:405710024|RGD:405855429|RGD:405866752|RGD:407573553 (Homo sapiens)
  • 1 RGD objects have been annotated to NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT AUTISM OR SEIZURES  (DOID:9004952)
  • 10 papers in RGD have been used to annotate CUL3
  • Curation Notes: ClinVar Annotator: match by term: Neurodevelopmental disorder with or without autism or seizures
  • Original References(s): PMID:25741868


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