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GENE - TERM ANNOTATION REPORT

8 Annotations Found.

An association has been curated linking ALKBH8 and autosomal recessive intellectual developmental disorder 71 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 autosomal recessive intellectual developmental disorder 71  (DOID:0081232)
  • 2 papers in RGD have been used to annotate ALKBH8


    • An association has been curated linking ALKBH8 and autosomal recessive intellectual developmental disorder 71 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:155644547 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal recessive intellectual developmental disorder 71  (DOID:0081232)
  • 2 papers in RGD have been used to annotate ALKBH8
  • Curation Notes: ClinVar Annotator: match by term: Intellectual developmental disorder, autosomal recessive 71
  • Original References(s): PMID:33544954


    • An association has been curated linking ALKBH8 and autosomal recessive intellectual developmental disorder 71 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:15116896 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal recessive intellectual developmental disorder 71  (DOID:0081232)
  • 2 papers in RGD have been used to annotate ALKBH8
  • Curation Notes: ClinVar Annotator: match by term: Intellectual developmental disorder, autosomal recessive 71
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking ALKBH8 and autosomal recessive intellectual developmental disorder 71 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:14698719 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal recessive intellectual developmental disorder 71  (DOID:0081232)
  • 2 papers in RGD have been used to annotate ALKBH8
  • Curation Notes: ClinVar Annotator: match by term: Intellectual developmental disorder, autosomal recessive 71
  • Original References(s): PMID:25741916 PMID:31079898


    • An association has been curated linking ALKBH8 and autosomal recessive intellectual developmental disorder 71 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:14698720 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal recessive intellectual developmental disorder 71  (DOID:0081232)
  • 2 papers in RGD have been used to annotate ALKBH8
  • Curation Notes: ClinVar Annotator: match by term: Intellectual developmental disorder, autosomal recessive 71
  • Original References(s): PMID:31079898


    • An association has been curated linking ALKBH8 and autosomal recessive intellectual developmental disorder 71 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:405281704 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal recessive intellectual developmental disorder 71  (DOID:0081232)
  • 2 papers in RGD have been used to annotate ALKBH8
  • Curation Notes: ClinVar Annotator: match by term: Intellectual developmental disorder, autosomal recessive 71
  • Original References(s): PMID:25741916


    • An association has been curated linking ALKBH8 and autosomal recessive intellectual developmental disorder 71 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:127261707|RGD:150545632|RGD:152088422 (Homo sapiens) & RGD:127261707|RGD:150545632|RGD:152088422 (Homo sapiens) & RGD:127261707|RGD:150545632|RGD:152088422 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal recessive intellectual developmental disorder 71  (DOID:0081232)
  • 2 papers in RGD have been used to annotate ALKBH8
  • Curation Notes: ClinVar Annotator: match by term: Intellectual developmental disorder, autosomal recessive 71


    • An association has been curated linking ALKBH8 and autosomal recessive intellectual developmental disorder 71 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:150404628|RGD:150404702|RGD:150404704|RGD:150404705|RGD:150557061|RGD:243051525 (Homo sapiens) & RGD:150404628|RGD:150404702|RGD:150404704|RGD:150404705|RGD:150557061|RGD:243051525 (Homo sapiens) & RGD:150404628|RGD:150404702|RGD:150404704|RGD:150404705|RGD:150557061|RGD:243051525 (Homo sapiens) & RGD:150404628|RGD:150404702|RGD:150404704|RGD:150404705|RGD:150557061|RGD:243051525 (Homo sapiens) & RGD:150404628|RGD:150404702|RGD:150404704|RGD:150404705|RGD:150557061|RGD:243051525 (Homo sapiens) & RGD:150404628|RGD:150404702|RGD:150404704|RGD:150404705|RGD:150557061|RGD:243051525 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal recessive intellectual developmental disorder 71  (DOID:0081232)
  • 2 papers in RGD have been used to annotate ALKBH8
  • Curation Notes: ClinVar Annotator: match by term: Intellectual developmental disorder, autosomal recessive 71
  • Original References(s): PMID:25741868


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