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 Variants Community Projects QTLs Strains Markers Genome Information Ontologies Cell Lines References Download Submit Data
OntoMate (Literature Search) JBrowse (Genome Browser) Synteny Browser (VCMap) Variant Visualizer Multi-Ontology Enrichment (MOET) Gene-Ortholog Location Finder (GOLF) InterViewer (Protein-Protein Interactions) PhenoMiner (Quatitative Phenotypes) Gene Annotator OLGA (Gene List Generator) AllianceMine GViewer (Genome Viewer)
Aging & Age-Related Disease Cancer & Neoplastic Disease Cardiovascular Disease Coronavirus Disease 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 Genetic Models Autism Models Rat PhenoMiner (Quantitative Phenotypes) Chinchilla PhenoMiner Expected Ranges (Quantitative Phenotype) PhenoMiner Term Comparison Hybrid Rat Diversity Panel Phenotypes 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 Presentations Archive Nomenclature Guidelines Resource Links Laboratory Resources Employment Resources
Advanced Search (OLGA)

GENE - TERM ANNOTATION REPORT

9 Annotations Found.

An association has been curated linking WFS1 and Wolfram syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from Inoue H, etal., Nat Genet. 1998 Oct;20(2):143-8.
  • 2 additional annotations were made from Inoue H, etal., Nat Genet. 1998 Oct;20(2):143-8.
  • 10 RGD objects have been annotated to Wolfram syndrome  (DOID:10632)
  • 24 papers in RGD have been used to annotate WFS1


    • An association has been curated linking WFS1 and Wolfram syndrome 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
  • 10 RGD objects have been annotated to Wolfram syndrome  (DOID:10632)
  • 24 papers in RGD have been used to annotate WFS1
  • Curation Notes: CTD Direct Evidence: marker/mechanism
  • Original References(s): PMID:24705017


    • An association has been curated linking WFS1 and Wolfram syndrome 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:8558125 (Homo sapiens)
  • 10 RGD objects have been annotated to Wolfram syndrome  (DOID:10632)
  • 24 papers in RGD have been used to annotate WFS1
  • Curation Notes: ClinVar Annotator: match by term: Wolfram syndrome
  • Original References(s): PMID:11161832 PMID:1161832 PMID:12955714 PMID:15151504 PMID:21446023 PMID:21602428 PMID:22238590 PMID:23429432 PMID:25741868 PMID:26875006 PMID:28492532 PMID:32141364


    • An association has been curated linking WFS1 and Wolfram syndrome 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:13216274 (Homo sapiens)
  • 10 RGD objects have been annotated to Wolfram syndrome  (DOID:10632)
  • 24 papers in RGD have been used to annotate WFS1
  • Curation Notes: ClinVar Annotator: match by term: Diabetes mellitus AND insipidus with optic atrophy AND deafness
  • Original References(s): PMID:10521293 PMID:16806192 PMID:25741868 PMID:28432734 PMID:28492532 PMID:30773290


    • An association has been curated linking WFS1 and Wolfram syndrome 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:151236084 (Homo sapiens)
  • 10 RGD objects have been annotated to Wolfram syndrome  (DOID:10632)
  • 24 papers in RGD have been used to annotate WFS1
  • Curation Notes: ClinVar Annotator: match by term: Diabetes mellitus AND insipidus with optic atrophy AND deafness


    • An association has been curated linking WFS1 and Wolfram syndrome 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:151236141 (Homo sapiens)
  • 10 RGD objects have been annotated to Wolfram syndrome  (DOID:10632)
  • 24 papers in RGD have been used to annotate WFS1
  • Curation Notes: ClinVar Annotator: match by term: Diabetes mellitus AND insipidus with optic atrophy AND deafness
  • Original References(s): PMID:12955714 PMID:17603484 PMID:18060660 PMID:20301750 PMID:20738327 PMID:33879153


    • An association has been curated linking WFS1 and Wolfram syndrome 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:10403453|RGD:10406088 (Homo sapiens) & RGD:10403453|RGD:10406088 (Homo sapiens)
  • 10 RGD objects have been annotated to Wolfram syndrome  (DOID:10632)
  • 24 papers in RGD have been used to annotate WFS1
  • Curation Notes: ClinVar Annotator: match by term: Wolfram syndrome
  • Original References(s): PMID:25741868


    • An association has been curated linking WFS1 and Wolfram syndrome 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:12906981 (Homo sapiens)
  • 10 RGD objects have been annotated to Wolfram syndrome  (DOID:10632)
  • 24 papers in RGD have been used to annotate WFS1
  • Curation Notes: ClinVar Annotator: match by term: Wolfram syndrome
  • Original References(s): PMID:12754709 PMID:15277431 PMID:17568405 PMID:21446023 PMID:24890733 PMID:25741868 PMID:27395765 PMID:28492532 PMID:31567480 PMID:33046911 PMID:33841295 PMID:34426522 PMID:35469785 PMID:36098976 PMID:36208030 PMID:36227502 PMID:37508961 PMID:37510321


    • An association has been curated linking WFS1 and Wolfram syndrome 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:10049186 (Homo sapiens)
  • 10 RGD objects have been annotated to Wolfram syndrome  (DOID:10632)
  • 24 papers in RGD have been used to annotate WFS1
  • Curation Notes: ClinVar Annotator: match by term: Wolfram syndrome
  • Original References(s): PMID:11244483 PMID:12754709 PMID:15277431 PMID:17568405 PMID:19344068 PMID:21446023 PMID:22226368 PMID:23596069 PMID:24033266 PMID:24890733 PMID:25133958 PMID:25741868 PMID:26435059 PMID:27395765 PMID:28432734 PMID:28492532 PMID:29207974 PMID:30014265 PMID:30245029 PMID:30957632 PMID:31264968 PMID:31567480 PMID:31980526 PMID:33046911 PMID:33763535 PMID:34404380 PMID:35018440 PMID:36098976 PMID:36208030


    • Go Back to source page   Continue to Ontology report