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

4 Annotations Found.

An association has been curated linking LRP5 and osteogenesis imperfecta in Canis lupus familiaris.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from Automated assignment of GO, PW and RDO ISO annotations across species
  • The annotation has been inferred from sequence orthology with Lrp5 (Mus musculus)
  • 54 RGD objects have been annotated to osteogenesis imperfecta  (DOID:12347)
  • 0 papers in RGD have been used to annotate LRP5
  • Qualifier: treatment
  • Original References(s): PMID:24677211 REF_RGD_ID:12792279


    • An association has been curated linking LRP5 and osteogenesis imperfecta in Canis lupus familiaris.        

  • 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 LRP5 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 54 RGD objects have been annotated to osteogenesis imperfecta  (DOID:12347)
  • 0 papers in RGD have been used to annotate LRP5
  • Curation Notes: ClinVar Annotator: match by term: Osteogenesis imperfecta
  • Original References(s): PMID:11719191 PMID:11793484 PMID:12579474 PMID:14727154 PMID:15024691 PMID:15077203 PMID:15201508 PMID:15346351 PMID:15619672 PMID:15767861 PMID:15777745 PMID:15824851 PMID:15824861 PMID:15850991 PMID:15981244 PMID:16234968 PMID:16252235 PMID:16679074 PMID:17086708 PMID:17137849 PMID:17202888 PMID:17223614 PMID:17241106 PMID:17306638 PMID:17307038 PMID:17395706 PMID:17505772 PMID:17766366 PMID:18058054 PMID:18349089 PMID:18493104 PMID:18588671 PMID:18721193 PMID:18932002 PMID:19023643 PMID:24706814 PMID:25741868 PMID:26467025 PMID:28492532 PMID:30452590 PMID:30894705


    • An association has been curated linking LRP5 and osteogenesis imperfecta in Canis lupus familiaris.        

  • 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 LRP5 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 54 RGD objects have been annotated to osteogenesis imperfecta  (DOID:12347)
  • 0 papers in RGD have been used to annotate LRP5
  • Curation Notes: ClinVar Annotator: match by term: Lobstein disease | ClinVar Annotator: match by term: Osteogenesis imperfecta
  • Original References(s): PMID:11719191 PMID:11793484 PMID:12579474 PMID:14727154 PMID:15024691 PMID:15077203 PMID:15201508 PMID:15346351 PMID:15619672 PMID:15767861 PMID:15777745 PMID:15824851 PMID:15824861 PMID:15850991 PMID:15981244 PMID:16234968 PMID:16252235 PMID:16679074 PMID:17086708 PMID:17137849 PMID:17202888 PMID:17223614 PMID:17241106 PMID:17306638 PMID:17307038 PMID:17395706 PMID:17505772 PMID:17766366 PMID:18058054 PMID:18349089 PMID:18493104 PMID:18588671 PMID:18721193 PMID:18932002 PMID:19023643 PMID:19324841 PMID:24706814 PMID:25711638 PMID:25741868 PMID:26467025 PMID:28492532 PMID:30452590 PMID:30894705 PMID:33118644


    • An association has been curated linking LRP5 and osteogenesis imperfecta in Canis lupus familiaris.        

  • 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 LRP5 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 54 RGD objects have been annotated to osteogenesis imperfecta  (DOID:12347)
  • 0 papers in RGD have been used to annotate LRP5
  • Curation Notes: ClinVar Annotator: match by term: Osteogenesis imperfecta
  • Original References(s): PMID:11719191 PMID:11793484 PMID:12579474 PMID:14727154 PMID:15024691 PMID:15077203 PMID:15201508 PMID:15346351 PMID:15619672 PMID:15767861 PMID:15777745 PMID:15824851 PMID:15824861 PMID:15850991 PMID:15981244 PMID:16234968 PMID:16252235 PMID:16679074 PMID:17086708 PMID:17137849 PMID:17202888 PMID:17223614 PMID:17241106 PMID:17306638 PMID:17307038 PMID:17395706 PMID:17505772 PMID:17766366 PMID:18058054 PMID:18349089 PMID:18493104 PMID:18588671 PMID:18721193 PMID:18932002 PMID:19023643 PMID:19324841 PMID:24706814 PMID:25384351 PMID:25711638 PMID:25741868 PMID:26467025 PMID:28192794 PMID:28492532 PMID:28494495 PMID:30452590 PMID:30894705 PMID:33118644 PMID:34860240 PMID:35252483


    • Go Back to source page   Continue to Ontology report