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GENE - TERM ANNOTATION REPORT

6 Annotations Found.

An association has been curated linking UBE2T and Fanconi anemia complementation group T 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:150452747 (Homo sapiens)
  • 2 RGD objects have been annotated to Fanconi anemia complementation group T  (DOID:0111081)
  • 2 papers in RGD have been used to annotate UBE2T
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group T
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking UBE2T and Fanconi anemia complementation group T in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • 2 RGD objects have been annotated to Fanconi anemia complementation group T  (DOID:0111081)
  • 2 papers in RGD have been used to annotate UBE2T


    • An association has been curated linking UBE2T and Fanconi anemia complementation group T 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:10053553 (Homo sapiens)
  • 2 RGD objects have been annotated to Fanconi anemia complementation group T  (DOID:0111081)
  • 2 papers in RGD have been used to annotate UBE2T
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group T
  • Original References(s): PMID:25741868 PMID:26046368


    • An association has been curated linking UBE2T and Fanconi anemia complementation group T in Homo sapiens.        

  • The association was inferred from experiment (EXP)
    		•  
  • The annotation was made from RGD automated import pipeline for CTD gene-to-disease annotations
  • 2 RGD objects have been annotated to Fanconi anemia complementation group T  (DOID:0111081)
  • 2 papers in RGD have been used to annotate UBE2T
  • Curation Notes: CTD Direct Evidence: marker/mechanism


    • An association has been curated linking UBE2T and Fanconi anemia complementation group T 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:34889186|RGD:34889187 (Homo sapiens) & RGD:34889186|RGD:34889187 (Homo sapiens)
  • 2 RGD objects have been annotated to Fanconi anemia complementation group T  (DOID:0111081)
  • 2 papers in RGD have been used to annotate UBE2T
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group T
  • Original References(s): PMID:26119737


    • An association has been curated linking UBE2T and Fanconi anemia complementation group T 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:10053554|RGD:34889188 (Homo sapiens) & RGD:10053554|RGD:34889188 (Homo sapiens)
  • 2 RGD objects have been annotated to Fanconi anemia complementation group T  (DOID:0111081)
  • 2 papers in RGD have been used to annotate UBE2T
  • Curation Notes: ClinVar Annotator: match by term: Fanconi anemia complementation group T
  • Original References(s): PMID:26046368


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