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

3 Annotations Found.

An association has been curated linking Nlrp12 and familial cold autoinflammatory syndrome 2 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • The annotation has been inferred from sequence orthology with NLRP12 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to familial cold autoinflammatory syndrome 2  (DOID:0090063)
  • 6 papers in RGD have been used to annotate Nlrp12


    • An association has been curated linking Nlrp12 and familial cold autoinflammatory syndrome 2 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from RGD automated import pipeline for CTD gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with NLRP12 (Homo sapiens) [(EXP) inferred from experiment]
  • 4 RGD objects have been annotated to familial cold autoinflammatory syndrome 2  (DOID:0090063)
  • 6 papers in RGD have been used to annotate Nlrp12
  • Curation Notes: CTD Direct Evidence: marker/mechanism


    • An association has been curated linking Nlrp12 and familial cold autoinflammatory syndrome 2 in Rattus norvegicus.        

  • 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 NLRP12 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to familial cold autoinflammatory syndrome 2  (DOID:0090063)
  • 6 papers in RGD have been used to annotate Nlrp12
  • Curation Notes: ClinVar Annotator: match by term: Familial cold autoinflammatory syndrome 2 | ClinVar Annotator: match by term: NLRP12-related condition
  • Original References(s): PMID:16199547 PMID:17576681 PMID:18230725 PMID:21360512 PMID:21538323 PMID:24033266 PMID:24064030 PMID:25064839 PMID:25640679 PMID:25741868 PMID:26508570 PMID:27314497 PMID:27633793 PMID:28492532 PMID:29500522 PMID:29951964 PMID:30783801 PMID:30788684 PMID:30858956 PMID:31155445 PMID:31820221 PMID:32868390 PMID:32888943 PMID:33042144 PMID:33165748 PMID:34298581 PMID:34725261 PMID:34975878 PMID:35482138 PMID:37928541 PMID:38123482 PMID:38343435 PMID:9536098


    • Go Back to source page   Continue to Ontology report