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

1 Annotations Found.

An association has been curated linking Pygm and genetic disease in Ictidomys tridecemlineatus.        

  • 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 PYGM (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 11814 RGD objects have been annotated to genetic disease  (DOID:630)
  • 0 papers in RGD have been used to annotate Pygm
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:10450796 PMID:1067063 PMID:11168025 PMID:11706962 PMID:12929201 PMID:14748827 PMID:16199547 PMID:16786513 PMID:17221871 PMID:17324573 PMID:17404776 PMID:17915571 PMID:19251976 PMID:20301518 PMID:21802952 PMID:22250184 PMID:22730558 PMID:23653251 PMID:2391551 PMID:24033266 PMID:25240406 PMID:25740218 PMID:25741868 PMID:25873271 PMID:25914343 PMID:26913921 PMID:2703328 PMID:28492532 PMID:29143597 PMID:29881221 PMID:30415384 PMID:32386344 PMID:34426522 PMID:3476861 PMID:35741838 PMID:8279469 PMID:8316268 PMID:8401511 PMID:9131647 PMID:9152836 PMID:9506549 PMID:9674815


    • Go Back to source page   Continue to Ontology report