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

RGD ID: 12536009
Species: Ictidomys tridecemlineatus
RGD Object: Gene
Symbol: Bmpr1a
Name: bone morphogenetic protein receptor type 1A
Acc ID: DOID:5295
Term: intestinal disease
Definition: A gastrointestinal system disease that is located_in the intestine. (DO)
Definition Source(s): http://en.wikipedia.org/wiki/Human_gastrointestinal_tract "DO" "DO"
Note: Use of the qualifier "multiple interactions" designates that the annotated interaction is comprised of a complex set of reactions and/or regulatory events, possibly involving additional chemicals and/or gene products.
Object SymbolQualifierEvidenceWithReferenceSourceNotesOriginal Reference(s)
Bmpr1a ISOBMPR1A (Homo sapiens)9068941RGDhereditary mixed polyposis syndrome-2, HMPS2, OMIM:610069, DNA:deletion:exonPMID:16525031 REF_RGD_ID:1600590
Bmpr1a ISOBMPR1A (Homo sapiens)9068941RGDjuvenile polyposis syndrome, OMIM:174900 , DNA:deletionPMID:16685657 REF_RGD_ID:1600591
Bmpr1a ISOBMPR1A (Homo sapiens)9068941RGDjuvenile polyposis, OMIM:174900, DNA:point mutation:exon:Q239XPMID:11381269 REF_RGD_ID:1600589
Go Back to source page   Continue to Ontology report