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GENE - TERM ANNOTATION REPORT

21 Annotations Found.

An association has been curated linking UGT1A9 and Crigler Najjar Syndrome, Type 2 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:13216293 (Homo sapiens)
  • 10 RGD objects have been annotated to Crigler Najjar Syndrome, Type 2  (DOID:9001862)
  • 8 papers in RGD have been used to annotate UGT1A9
  • Curation Notes: ClinVar Annotator: match by term: Crigler Najjar syndrome, type 2
  • Original References(s): PMID:18058623 PMID:19830808 PMID:25741868 PMID:8514037 PMID:9621515


    • An association has been curated linking UGT1A9 and Crigler Najjar Syndrome, Type 2 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:8563025 (Homo sapiens)
  • 10 RGD objects have been annotated to Crigler Najjar Syndrome, Type 2  (DOID:9001862)
  • 8 papers in RGD have been used to annotate UGT1A9
  • Curation Notes: ClinVar Annotator: match by term: Crigler Najjar syndrome, type 2
  • Original References(s): PMID:12402338 PMID:24492252


    • An association has been curated linking UGT1A9 and Crigler Najjar Syndrome, Type 2 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:151757095 (Homo sapiens)
  • 10 RGD objects have been annotated to Crigler Najjar Syndrome, Type 2  (DOID:9001862)
  • 8 papers in RGD have been used to annotate UGT1A9
  • Curation Notes: ClinVar Annotator: match by term: Crigler Najjar syndrome, type 2
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking UGT1A9 and Crigler Najjar Syndrome, Type 2 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:13704789 (Homo sapiens)
  • 10 RGD objects have been annotated to Crigler Najjar Syndrome, Type 2  (DOID:9001862)
  • 8 papers in RGD have been used to annotate UGT1A9
  • Curation Notes: ClinVar Annotator: match by term: Crigler-Najjar syndrome, type II
  • Original References(s): PMID:25741868 PMID:25822733


    • An association has been curated linking UGT1A9 and Crigler Najjar Syndrome, Type 2 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:8563019 (Homo sapiens)
  • 10 RGD objects have been annotated to Crigler Najjar Syndrome, Type 2  (DOID:9001862)
  • 8 papers in RGD have been used to annotate UGT1A9
  • Curation Notes: ClinVar Annotator: match by term: Crigler Najjar syndrome, type 2
  • Original References(s): PMID:10412811 PMID:10472535 PMID:11061796 PMID:12502904 PMID:15304120 PMID:17850628 PMID:18004206 PMID:19243019 PMID:19390945 PMID:19397531 PMID:19830808 PMID:20975617 PMID:21272068 PMID:21319362 PMID:21342357 PMID:23014115 PMID:24033692 PMID:25200497 PMID:25741868 PMID:26467025 PMID:26604633 PMID:26830078 PMID:26857783 PMID:27220761 PMID:28492532 PMID:28520360 PMID:28585035 PMID:9630669 PMID:9784835 PMID:9929972


    • An association has been curated linking UGT1A9 and Crigler Najjar Syndrome, Type 2 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:8563009 (Homo sapiens)
  • 10 RGD objects have been annotated to Crigler Najjar Syndrome, Type 2  (DOID:9001862)
  • 8 papers in RGD have been used to annotate UGT1A9
  • Curation Notes: ClinVar Annotator: match by term: Crigler-Najjar syndrome, type II
  • Original References(s): PMID:1692835 PMID:25741868 PMID:805737 PMID:8276413


    • An association has been curated linking UGT1A9 and Crigler Najjar Syndrome, Type 2 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:8563020 (Homo sapiens)
  • 10 RGD objects have been annotated to Crigler Najjar Syndrome, Type 2  (DOID:9001862)
  • 8 papers in RGD have been used to annotate UGT1A9
  • Curation Notes: ClinVar Annotator: match by term: Crigler Najjar syndrome, type 2
  • Original References(s): PMID:11061796 PMID:11983459 PMID:12181437 PMID:12485959 PMID:15304109 PMID:15304120 PMID:18004206 PMID:18414213 PMID:18419642 PMID:21297505 PMID:21319362 PMID:22169899 PMID:24033266 PMID:24749086 PMID:25741868 PMID:26250421 PMID:28492532 PMID:29137095 PMID:9630669


    • An association has been curated linking UGT1A9 and Crigler Najjar Syndrome, Type 2 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:8563013 (Homo sapiens)
  • 10 RGD objects have been annotated to Crigler Najjar Syndrome, Type 2  (DOID:9001862)
  • 8 papers in RGD have been used to annotate UGT1A9
  • Curation Notes: ClinVar Annotator: match by term: Crigler Najjar syndrome, type 2
  • Original References(s): PMID:11316168 PMID:12181437 PMID:14616765 PMID:15304120 PMID:1692835 PMID:18004206 PMID:18414213 PMID:19325249 PMID:24033266 PMID:25200497 PMID:25741868 PMID:25755387 PMID:28492532 PMID:29137095 PMID:30544479 PMID:31467903 PMID:6480579 PMID:7715297 PMID:8528206 PMID:9621515


    • An association has been curated linking UGT1A9 and Crigler Najjar Syndrome, Type 2 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:10052444 (Homo sapiens)
  • 10 RGD objects have been annotated to Crigler Najjar Syndrome, Type 2  (DOID:9001862)
  • 8 papers in RGD have been used to annotate UGT1A9
  • Curation Notes: ClinVar Annotator: match by term: Crigler Najjar syndrome, type 2
  • Original References(s): PMID:19325249 PMID:25200497 PMID:25741868 PMID:26727668 PMID:28492532


    • An association has been curated linking UGT1A9 and Crigler Najjar Syndrome, Type 2 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:8563026 (Homo sapiens)
  • 10 RGD objects have been annotated to Crigler Najjar Syndrome, Type 2  (DOID:9001862)
  • 8 papers in RGD have been used to annotate UGT1A9
  • Curation Notes: ClinVar Annotator: match by term: Crigler-Najjar syndrome, type II
  • Original References(s): PMID:14550264 PMID:25741868 PMID:8706880


    • An association has been curated linking UGT1A9 and Crigler Najjar Syndrome, Type 2 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:13516025 (Homo sapiens)
  • 10 RGD objects have been annotated to Crigler Najjar Syndrome, Type 2  (DOID:9001862)
  • 8 papers in RGD have been used to annotate UGT1A9
  • Curation Notes: ClinVar Annotator: match by term: Crigler Najjar syndrome, type 2
  • Original References(s): PMID:15712364 PMID:18058623 PMID:25741868 PMID:28492532


    • An association has been curated linking UGT1A9 and Crigler Najjar Syndrome, Type 2 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:150411136 (Homo sapiens)
  • 10 RGD objects have been annotated to Crigler Najjar Syndrome, Type 2  (DOID:9001862)
  • 8 papers in RGD have been used to annotate UGT1A9
  • Curation Notes: ClinVar Annotator: match by term: Crigler-Najjar syndrome, type II
  • Original References(s): PMID:11013440 PMID:23290513 PMID:25741868 PMID:28492532


    • An association has been curated linking UGT1A9 and Crigler Najjar Syndrome, Type 2 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:11638587 (Homo sapiens)
  • 10 RGD objects have been annotated to Crigler Najjar Syndrome, Type 2  (DOID:9001862)
  • 8 papers in RGD have been used to annotate UGT1A9
  • Curation Notes: ClinVar Annotator: match by term: Crigler Najjar syndrome, type 2
  • Original References(s): PMID:23099197 PMID:25741868 PMID:28492532


    • An association has been curated linking UGT1A9 and Crigler Najjar Syndrome, Type 2 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:10405510 (Homo sapiens)
  • 10 RGD objects have been annotated to Crigler Najjar Syndrome, Type 2  (DOID:9001862)
  • 8 papers in RGD have been used to annotate UGT1A9
  • Curation Notes: ClinVar Annotator: match by term: Crigler Najjar syndrome, type 2
  • Original References(s): PMID:10975608 PMID:12105841 PMID:12208142 PMID:15304120 PMID:16610035 PMID:21726413 PMID:25741868 PMID:25993113 PMID:26727668 PMID:27264814 PMID:28492532 PMID:29137095 PMID:30669781 PMID:31450232 PMID:31737051 PMID:31858773 PMID:33083013 PMID:34953813 PMID:35257483 PMID:35426266 PMID:35436954 PMID:35781232


    • An association has been curated linking UGT1A9 and Crigler Najjar Syndrome, Type 2 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:11643761 (Homo sapiens)
  • 10 RGD objects have been annotated to Crigler Najjar Syndrome, Type 2  (DOID:9001862)
  • 8 papers in RGD have been used to annotate UGT1A9
  • Curation Notes: ClinVar Annotator: match by term: Crigler Najjar syndrome, type 2
  • Original References(s): PMID:23875061 PMID:25741868 PMID:28492532


    • An association has been curated linking UGT1A9 and Crigler Najjar Syndrome, Type 2 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:9684143 (Homo sapiens)
  • 10 RGD objects have been annotated to Crigler Najjar Syndrome, Type 2  (DOID:9001862)
  • 8 papers in RGD have been used to annotate UGT1A9
  • Curation Notes: ClinVar Annotator: match by term: Crigler-Najjar syndrome, type II
  • Original References(s): PMID:18414213 PMID:25741868 PMID:26716871 PMID:28492532 PMID:31145902


    • An association has been curated linking UGT1A9 and Crigler Najjar Syndrome, Type 2 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:13522555 (Homo sapiens)
  • 10 RGD objects have been annotated to Crigler Najjar Syndrome, Type 2  (DOID:9001862)
  • 8 papers in RGD have been used to annotate UGT1A9
  • Curation Notes: ClinVar Annotator: match by term: Crigler Najjar syndrome, type 2
  • Original References(s): PMID:11013440 PMID:17229650 PMID:18058623 PMID:25741868 PMID:28492532


    • An association has been curated linking UGT1A9 and Crigler Najjar Syndrome, Type 2 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:401915981 (Homo sapiens)
  • 10 RGD objects have been annotated to Crigler Najjar Syndrome, Type 2  (DOID:9001862)
  • 8 papers in RGD have been used to annotate UGT1A9
  • Curation Notes: ClinVar Annotator: match by term: Crigler-Najjar syndrome, type II


    • An association has been curated linking UGT1A9 and Crigler Najjar Syndrome, Type 2 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:8563027 (Homo sapiens)
  • 10 RGD objects have been annotated to Crigler Najjar Syndrome, Type 2  (DOID:9001862)
  • 8 papers in RGD have been used to annotate UGT1A9
  • Curation Notes: ClinVar Annotator: match by term: Crigler Najjar syndrome, type 2
  • Original References(s): PMID:11906189 PMID:15378351 PMID:25741868 PMID:32860008


    • An association has been curated linking UGT1A9 and Crigler Najjar Syndrome, Type 2 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:8563024 (Homo sapiens)
  • 10 RGD objects have been annotated to Crigler Najjar Syndrome, Type 2  (DOID:9001862)
  • 8 papers in RGD have been used to annotate UGT1A9
  • Curation Notes: ClinVar Annotator: match by term: Crigler Najjar syndrome, type 2
  • Original References(s): PMID:11013440 PMID:11370628 PMID:19830808 PMID:23290513 PMID:25741868 PMID:28492532 PMID:7989595 PMID:9028453


    • An association has been curated linking UGT1A9 and Crigler Najjar Syndrome, Type 2 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:11643075|RGD:13212926|RGD:151348757|RGD:151661964|RGD:156434181|RGD:401919680 (Homo sapiens) & RGD:11643075|RGD:13212926|RGD:151348757|RGD:151661964|RGD:156434181|RGD:401919680 (Homo sapiens) & RGD:11643075|RGD:13212926|RGD:151348757|RGD:151661964|RGD:156434181|RGD:401919680 (Homo sapiens) & RGD:11643075|RGD:13212926|RGD:151348757|RGD:151661964|RGD:156434181|RGD:401919680 (Homo sapiens) & RGD:11643075|RGD:13212926|RGD:151348757|RGD:151661964|RGD:156434181|RGD:401919680 (Homo sapiens) & RGD:11643075|RGD:13212926|RGD:151348757|RGD:151661964|RGD:156434181|RGD:401919680 (Homo sapiens)
  • 10 RGD objects have been annotated to Crigler Najjar Syndrome, Type 2  (DOID:9001862)
  • 8 papers in RGD have been used to annotate UGT1A9
  • Curation Notes: ClinVar Annotator: match by term: Crigler Najjar syndrome, type 2 | ClinVar Annotator: match by term: Crigler-Najjar syndrome, type II
  • Original References(s): PMID:25741868


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