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: 9016445
Species: Chinchilla lanigera
RGD Object: Gene
Symbol: F2
Name: coagulation factor II, thrombin
Acc ID: DOID:0060903
Term: thrombosis
Definition: A vascular disease caused by the formation of a blood clot inside a blood vessel, obstructing the flow of blood through the circulatory system. (DO)
Definition Source(s): https://en.wikipedia.org/wiki/Thrombosis "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)
F2 ISOF2 (Homo sapiens)9068941RGDDNA:mutation: :20210G>A (human)PMID:21070754 REF_RGD_ID:6893603
F2 ISOF2 (Rattus norvegicus)9068941RGD PMID:22402172 REF_RGD_ID:7387314
F2 ISOF2 (Mus musculus)9068941RGD PMID:21605330 REF_RGD_ID:7387259
F2no_associationISOF2 (Homo sapiens)9068941RGDassociated with Behcet Syndrome;DNA:mutation: :20210G>A (human)PMID:12632020 REF_RGD_ID:7394765
F2treatmentISOF2 (Rattus norvegicus)9068941RGD PMID:17293494 REF_RGD_ID:11035267
F2treatmentISOF2 (Mus musculus)9068941RGDassociated with Carotid Artery InjuriesPMID:15039280 REF_RGD_ID:10449423
F2 ISOF2 (Homo sapiens)9068941CTDCTD Direct Evidence: marker/mechanismPMID:10064001 PMID:11132655 PMID:1279834 PMID:17245631
Go Back to source page   Continue to Ontology report