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GENE - TERM ANNOTATION REPORT

50 Annotations Found.

An association has been curated linking TRMT1 and genetic disease 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:156095837 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 1 papers in RGD have been used to annotate TRMT1
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking TRMT1 and genetic disease 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:40886696 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 1 papers in RGD have been used to annotate TRMT1
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking TRMT1 and genetic disease 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:156142261 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 1 papers in RGD have been used to annotate TRMT1
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking TRMT1 and genetic disease 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:156382183 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 1 papers in RGD have been used to annotate TRMT1
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking TRMT1 and genetic disease 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:156178783 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 1 papers in RGD have been used to annotate TRMT1
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking TRMT1 and genetic disease 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:401777781 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 1 papers in RGD have been used to annotate TRMT1
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking TRMT1 and genetic disease 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:401759090 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 1 papers in RGD have been used to annotate TRMT1
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking TRMT1 and genetic disease 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:401755484 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 1 papers in RGD have been used to annotate TRMT1
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking TRMT1 and genetic disease 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:156307872 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 1 papers in RGD have been used to annotate TRMT1
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:25741868


  • An association has been curated linking TRMT1 and genetic disease 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:155976353 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 1 papers in RGD have been used to annotate TRMT1
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking TRMT1 and genetic disease 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:156065677 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 1 papers in RGD have been used to annotate TRMT1
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking TRMT1 and genetic disease 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:156400594 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 1 papers in RGD have been used to annotate TRMT1
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking TRMT1 and genetic disease 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:155921683 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 1 papers in RGD have been used to annotate TRMT1
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking TRMT1 and genetic disease 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:156122208 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 1 papers in RGD have been used to annotate TRMT1
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking TRMT1 and genetic disease 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:156382498 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 1 papers in RGD have been used to annotate TRMT1
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking TRMT1 and genetic disease 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:15115683 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 1 papers in RGD have been used to annotate TRMT1
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


  • An association has been curated linking TRMT1 and genetic disease 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:156265526 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 1 papers in RGD have been used to annotate TRMT1
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking TRMT1 and genetic disease 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:156150884 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 1 papers in RGD have been used to annotate TRMT1
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking TRMT1 and genetic disease 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:156097027 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 1 papers in RGD have been used to annotate TRMT1
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking TRMT1 and genetic disease 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:156095771 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 1 papers in RGD have been used to annotate TRMT1
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking TRMT1 and genetic disease 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:155993216 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 1 papers in RGD have been used to annotate TRMT1
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking TRMT1 and genetic disease 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:156216685 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 1 papers in RGD have been used to annotate TRMT1
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking TRMT1 and genetic disease 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:126744090 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 1 papers in RGD have been used to annotate TRMT1
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:25741868


  • An association has been curated linking TRMT1 and genetic disease 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:156139094 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 1 papers in RGD have been used to annotate TRMT1
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking TRMT1 and genetic disease 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:156365450 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 1 papers in RGD have been used to annotate TRMT1
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking TRMT1 and genetic disease 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:156233604 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 1 papers in RGD have been used to annotate TRMT1
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking TRMT1 and genetic disease 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:156326213 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 1 papers in RGD have been used to annotate TRMT1
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking TRMT1 and genetic disease 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:156079392 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 1 papers in RGD have been used to annotate TRMT1
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking TRMT1 and genetic disease 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:156256197 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 1 papers in RGD have been used to annotate TRMT1
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking TRMT1 and genetic disease 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:155929006 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 1 papers in RGD have been used to annotate TRMT1
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking TRMT1 and genetic disease 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:155927094 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 1 papers in RGD have been used to annotate TRMT1
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking TRMT1 and genetic disease 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:156078875 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 1 papers in RGD have been used to annotate TRMT1
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking TRMT1 and genetic disease 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:156114781 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 1 papers in RGD have been used to annotate TRMT1
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking TRMT1 and genetic disease 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:156077923 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 1 papers in RGD have been used to annotate TRMT1
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking TRMT1 and genetic disease 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:156060247 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 1 papers in RGD have been used to annotate TRMT1
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking TRMT1 and genetic disease 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:156063670 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 1 papers in RGD have been used to annotate TRMT1
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking TRMT1 and genetic disease 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:155930683 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 1 papers in RGD have been used to annotate TRMT1
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking TRMT1 and genetic disease 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:156147537 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 1 papers in RGD have been used to annotate TRMT1
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking TRMT1 and genetic disease 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:156331493 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 1 papers in RGD have been used to annotate TRMT1
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking TRMT1 and genetic disease 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:156149988 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 1 papers in RGD have been used to annotate TRMT1
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking TRMT1 and genetic disease 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:156368569 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 1 papers in RGD have been used to annotate TRMT1
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking TRMT1 and genetic disease 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:401719875 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 1 papers in RGD have been used to annotate TRMT1
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking TRMT1 and genetic disease 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:401766861 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 1 papers in RGD have been used to annotate TRMT1
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking TRMT1 and genetic disease 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:401769707 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 1 papers in RGD have been used to annotate TRMT1
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking TRMT1 and genetic disease 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:401759018 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 1 papers in RGD have been used to annotate TRMT1
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking TRMT1 and genetic disease 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:401739279 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 1 papers in RGD have been used to annotate TRMT1
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking TRMT1 and genetic disease 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:401870554 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 1 papers in RGD have been used to annotate TRMT1
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking TRMT1 and genetic disease 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:401867414 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 1 papers in RGD have been used to annotate TRMT1
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking TRMT1 and genetic disease 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:401895309 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 1 papers in RGD have been used to annotate TRMT1
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


  • An association has been curated linking TRMT1 and genetic disease 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:401899993 (Homo sapiens)
  • 32754 RGD objects have been annotated to genetic disease  (DOID:630)
  • 1 papers in RGD have been used to annotate TRMT1
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


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