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GENE - TERM ANNOTATION REPORT

6 Annotations Found.

An association has been curated linking RAB11B and Neurodevelopmental Disorder with Ataxic Gait, Absent Speech, and Decreased Cortical White Matter 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:13489123 (Homo sapiens)
  • 1 RGD objects have been annotated to Neurodevelopmental Disorder with Ataxic Gait, Absent Speech, and Decreased Cortical White Matter  (DOID:9009096)
  • 3 papers in RGD have been used to annotate RAB11B
  • Curation Notes: ClinVar Annotator: match by term: Neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matter
  • Original References(s): PMID:25741868 PMID:29106825


    • An association has been curated linking RAB11B and Neurodevelopmental Disorder with Ataxic Gait, Absent Speech, and Decreased Cortical White Matter 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 Ataxic Gait, Absent Speech, and Decreased Cortical White Matter  (DOID:9009096)
  • 3 papers in RGD have been used to annotate RAB11B


    • An association has been curated linking RAB11B and Neurodevelopmental Disorder with Ataxic Gait, Absent Speech, and Decreased Cortical White Matter 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:151662299 (Homo sapiens)
  • 1 RGD objects have been annotated to Neurodevelopmental Disorder with Ataxic Gait, Absent Speech, and Decreased Cortical White Matter  (DOID:9009096)
  • 3 papers in RGD have been used to annotate RAB11B
  • Curation Notes: ClinVar Annotator: match by term: Neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matter


    • An association has been curated linking RAB11B and Neurodevelopmental Disorder with Ataxic Gait, Absent Speech, and Decreased Cortical White Matter 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:126741942|RGD:152979412|RGD:405000614 (Homo sapiens) & RGD:126741942|RGD:152979412|RGD:405000614 (Homo sapiens) & RGD:126741942|RGD:152979412|RGD:405000614 (Homo sapiens)
  • 1 RGD objects have been annotated to Neurodevelopmental Disorder with Ataxic Gait, Absent Speech, and Decreased Cortical White Matter  (DOID:9009096)
  • 3 papers in RGD have been used to annotate RAB11B
  • Curation Notes: ClinVar Annotator: match by term: Neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matter
  • Original References(s): PMID:25741868


    • An association has been curated linking RAB11B and Neurodevelopmental Disorder with Ataxic Gait, Absent Speech, and Decreased Cortical White Matter 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:13477090|RGD:155798819 (Homo sapiens) & RGD:13477090|RGD:155798819 (Homo sapiens)
  • 1 RGD objects have been annotated to Neurodevelopmental Disorder with Ataxic Gait, Absent Speech, and Decreased Cortical White Matter  (DOID:9009096)
  • 3 papers in RGD have been used to annotate RAB11B
  • Curation Notes: ClinVar Annotator: match by term: Neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matter
  • Original References(s): PMID:25741868 PMID:28492532 PMID:29106825


    • An association has been curated linking RAB11B and Neurodevelopmental Disorder with Ataxic Gait, Absent Speech, and Decreased Cortical White Matter 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:15162715|RGD:156189578 (Homo sapiens) & RGD:15162715|RGD:156189578 (Homo sapiens)
  • 1 RGD objects have been annotated to Neurodevelopmental Disorder with Ataxic Gait, Absent Speech, and Decreased Cortical White Matter  (DOID:9009096)
  • 3 papers in RGD have been used to annotate RAB11B
  • Curation Notes: ClinVar Annotator: match by term: Neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matter
  • Original References(s): PMID:25741868 PMID:28492532


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