Send us a Message



 Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   
Search RGD Grant Resources Citing RGD About Us Contact Us
Genes QTLs Strains Markers Genome Information Ontologies Cell Lines References Download Submit Data
OntoMate (Literature Search) JBrowse (Genome Browser) Variant Visualizer Multi-Ontology Enrichment (MOET) Gene-Ortholog Location Finder (GOLF) InterViewer (Protein-Protein Interactions) PhenoMiner (Quatitative Phenotypes) Gene Annotator OLGA (Gene List Generator) RatMine GViewer (Genome Viewer) Overgo Probe Designer ACP Haplotyper Genome Scanner VCMap
Aging & Age-Related Disease Cancer Cardiovascular Disease COVID-19 Developmental Disease Diabetes Hematologic Disease Immune & Inflammatory Disease Infectious Disease Liver Disease Neurological Disease Obesity & Metabolic Syndrome Renal Disease Respiratory Disease Sensory Organ Disease
Find Models   new Genetic Models Autism Models PhenoMiner (Quantitative Phenotypes) Expected Ranges (Quantitative Phenotype) PhenoMiner Term Comparison Hybrid Rat Diversity Panel Phenotypes GERRC (Gene Editing Rat Resource Center) Phenotypes in Other Animal Models Animal Husbandry Strain Medical Records Phylogenetics Strain Availability Calendar Rats 101 Submissions Photo Archive
Pathways
Rat Community Forum Directory of Rat Laboratories Video Tutorials News RGD Publications RGD Poster Archive Nomenclature Guidelines Resource Links Laboratory Resources Employment Resources

GENE - TERM ANNOTATION REPORT

11 Annotations Found.

An association has been curated linking Ugt1a2 and Crigler Najjar Syndrome, Type 2 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • 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 from sequence orthology with UGT1A3 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 7 RGD objects have been annotated to Crigler Najjar Syndrome, Type 2  (DOID:9001862)
  • 10 papers in RGD have been used to annotate Ugt1a2
  • Curation Notes: ClinVar Annotator: match by term: Crigler-Najjar syndrome, type II
  • Original References(s): PMID:1692835 PMID:805737 PMID:8276413


    • An association has been curated linking Ugt1a2 and Crigler Najjar Syndrome, Type 2 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • 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 from sequence orthology with UGT1A3 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 7 RGD objects have been annotated to Crigler Najjar Syndrome, Type 2  (DOID:9001862)
  • 10 papers in RGD have been used to annotate Ugt1a2
  • Curation Notes: ClinVar Annotator: match by term: HYPERBILIRUBINEMIA, CRIGLER-NAJJAR TYPE II
  • Original References(s): PMID:11061796 PMID:18004206 PMID:18414213 PMID:25741868


    • An association has been curated linking Ugt1a2 and Crigler Najjar Syndrome, Type 2 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • 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 from sequence orthology with UGT1A3 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 7 RGD objects have been annotated to Crigler Najjar Syndrome, Type 2  (DOID:9001862)
  • 10 papers in RGD have been used to annotate Ugt1a2
  • Curation Notes: ClinVar Annotator: match by term: Crigler-Najjar syndrome, type II
  • Original References(s): PMID:14550264 PMID:8706880


    • An association has been curated linking Ugt1a2 and Crigler Najjar Syndrome, Type 2 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • 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 from sequence orthology with UGT1A3 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 7 RGD objects have been annotated to Crigler Najjar Syndrome, Type 2  (DOID:9001862)
  • 10 papers in RGD have been used to annotate Ugt1a2
  • Curation Notes: ClinVar Annotator: match by term: Crigler-Najjar syndrome, type II
  • Original References(s): PMID:11370628


    • An association has been curated linking Ugt1a2 and Crigler Najjar Syndrome, Type 2 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • 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 from sequence orthology with UGT1A3 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 7 RGD objects have been annotated to Crigler Najjar Syndrome, Type 2  (DOID:9001862)
  • 10 papers in RGD have been used to annotate Ugt1a2
  • Curation Notes: ClinVar Annotator: match by term: Crigler-Najjar syndrome, type II
  • Original References(s): PMID:1692835 PMID:18004206 PMID:18414213 PMID:28492532 PMID:6480579 PMID:8528206 PMID:9621515


    • An association has been curated linking Ugt1a2 and Crigler Najjar Syndrome, Type 2 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • 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 from sequence orthology with UGT1A3 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 7 RGD objects have been annotated to Crigler Najjar Syndrome, Type 2  (DOID:9001862)
  • 10 papers in RGD have been used to annotate Ugt1a2
  • Curation Notes: ClinVar Annotator: match by term: HYPERBILIRUBINEMIA, CRIGLER-NAJJAR TYPE II
  • Original References(s): PMID:10412811 PMID:10472535 PMID:11061796 PMID:11156391 PMID:12181437 PMID:12502904 PMID:15304120 PMID:16636344 PMID:17627617 PMID:17850628 PMID:18004206 PMID:18221820 PMID:19243019 PMID:19299905 PMID:19390945 PMID:22992668 PMID:23014115 PMID:24033692 PMID:24308720 PMID:24448639 PMID:24519753 PMID:25285015 PMID:25741868 PMID:26229432 PMID:26604633 PMID:26830078 PMID:26857783 PMID:26862009 PMID:27220761 PMID:27385990 PMID:28367249 PMID:28520360 PMID:28585035 PMID:9784835 PMID:9929972


    • An association has been curated linking Ugt1a2 and Crigler Najjar Syndrome, Type 2 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • 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 from sequence orthology with UGT1A3 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 7 RGD objects have been annotated to Crigler Najjar Syndrome, Type 2  (DOID:9001862)
  • 10 papers in RGD have been used to annotate Ugt1a2
  • Curation Notes: ClinVar Annotator: match by term: HYPERBILIRUBINEMIA, CRIGLER-NAJJAR TYPE II
  • Original References(s): PMID:15712364 PMID:25741868


    • An association has been curated linking Ugt1a2 and Crigler Najjar Syndrome, Type 2 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • 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 from sequence orthology with UGT1A3 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 7 RGD objects have been annotated to Crigler Najjar Syndrome, Type 2  (DOID:9001862)
  • 10 papers in RGD have been used to annotate Ugt1a2
  • Curation Notes: ClinVar Annotator: match by term: Crigler-Najjar syndrome, type II
  • Original References(s): PMID:17229650


    • An association has been curated linking Ugt1a2 and Crigler Najjar Syndrome, Type 2 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • 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 from sequence orthology with UGT1A3 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 7 RGD objects have been annotated to Crigler Najjar Syndrome, Type 2  (DOID:9001862)
  • 10 papers in RGD have been used to annotate Ugt1a2
  • Curation Notes: ClinVar Annotator: match by term: HYPERBILIRUBINEMIA, CRIGLER-NAJJAR TYPE II
  • Original References(s): PMID:12402338 PMID:24492252


    • An association has been curated linking Ugt1a2 and Crigler Najjar Syndrome, Type 2 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • 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 from sequence orthology with UGT1A3 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 7 RGD objects have been annotated to Crigler Najjar Syndrome, Type 2  (DOID:9001862)
  • 10 papers in RGD have been used to annotate Ugt1a2
  • Curation Notes: ClinVar Annotator: match by term: Crigler Najjar syndrome, type 2
  • Original References(s): PMID:12208142 PMID:15304120 PMID:25741868 PMID:25993113 PMID:26727668 PMID:28492532


    • An association has been curated linking Ugt1a2 and Crigler Najjar Syndrome, Type 2 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • 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 from sequence orthology with UGT1A3 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 7 RGD objects have been annotated to Crigler Najjar Syndrome, Type 2  (DOID:9001862)
  • 10 papers in RGD have been used to annotate Ugt1a2
  • Curation Notes: ClinVar Annotator: match by term: Crigler Najjar syndrome, type 2
  • Original References(s): PMID:23875061 PMID:25741868


    • Go Back to source page   Continue to Ontology report