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GENE - TERM ANNOTATION REPORT

8 Annotations Found.

An association has been curated linking DGUOK 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:10401564 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 9 papers in RGD have been used to annotate DGUOK
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:25131622 PMID:25741868 PMID:28492532


    • An association has been curated linking DGUOK 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:10409265 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 9 papers in RGD have been used to annotate DGUOK
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:23043144 PMID:25741868 PMID:28492532 PMID:28902392 PMID:29137425 PMID:29228108 PMID:30283818 PMID:30393377 PMID:30956829 PMID:31664448


    • An association has been curated linking DGUOK 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:126741108 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 9 papers in RGD have been used to annotate DGUOK
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:25741868


    • An association has been curated linking DGUOK 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:10410565 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 9 papers in RGD have been used to annotate DGUOK
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking DGUOK 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:8597796 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 9 papers in RGD have been used to annotate DGUOK
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:12205643 PMID:14623087 PMID:19103789 PMID:27324545 PMID:28492532 PMID:28493820 PMID:30366773 PMID:32482602


    • An association has been curated linking DGUOK 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:150540376 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 9 papers in RGD have been used to annotate DGUOK
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:18205204 PMID:19380071 PMID:23141463 PMID:25741868 PMID:28492532


    • An association has been curated linking DGUOK 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:10409208|RGD:10410872|RGD:13835986|RGD:150422687 (Homo sapiens) & RGD:10409208|RGD:10410872|RGD:13835986|RGD:150422687 (Homo sapiens) & RGD:10409208|RGD:10410872|RGD:13835986|RGD:150422687 (Homo sapiens) & RGD:10409208|RGD:10410872|RGD:13835986|RGD:150422687 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 9 papers in RGD have been used to annotate DGUOK
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


    • An association has been curated linking DGUOK 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:156189536|RGD:156247876|RGD:156255824|RGD:156260636 (Homo sapiens) & RGD:156189536|RGD:156247876|RGD:156255824|RGD:156260636 (Homo sapiens) & RGD:156189536|RGD:156247876|RGD:156255824|RGD:156260636 (Homo sapiens) & RGD:156189536|RGD:156247876|RGD:156255824|RGD:156260636 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 9 papers in RGD have been used to annotate DGUOK
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


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