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   new 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

GENE - TERM ANNOTATION REPORT

2 Annotations Found.

An association has been curated linking MYBPC3 and Cardiac Conduction Defect 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:8605489 (Homo sapiens)
  • 24 RGD objects have been annotated to Cardiac Conduction Defect  (DOID:9001836)
  • 14 papers in RGD have been used to annotate MYBPC3
  • Curation Notes: ClinVar Annotator: match by term: cardiac conduction defect
  • Original References(s): PMID:18533079 PMID:20215591 PMID:21499742 PMID:21832025 PMID:21832052 PMID:21835320 PMID:22361390 PMID:23861362 PMID:24033266 PMID:24111713 PMID:25351510 PMID:25741868 PMID:26914223 PMID:28492532


    • An association has been curated linking MYBPC3 and Cardiac Conduction Defect 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:8602974 (Homo sapiens)
  • 24 RGD objects have been annotated to Cardiac Conduction Defect  (DOID:9001836)
  • 14 papers in RGD have been used to annotate MYBPC3
  • Curation Notes: ClinVar Annotator: match by term: cardiac conduction defect
  • Original References(s): PMID:15519027 PMID:16858239 PMID:17576681 PMID:18273486 PMID:18533079 PMID:21415409 PMID:22555271 PMID:23054336 PMID:24033266 PMID:24111713 PMID:24510615 PMID:25031304 PMID:25740977 PMID:25741868 PMID:27483260 PMID:27532257 PMID:27688314 PMID:28138913 PMID:28356264 PMID:28492532 PMID:28658286 PMID:28679633 PMID:28824454 PMID:28916354 PMID:28971120 PMID:34137518 PMID:9536098


    • Go Back to source page   Continue to Ontology report