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: 12468797
Species: Ictidomys tridecemlineatus
RGD Object: Gene
Symbol: Chrna2
Name: cholinergic receptor nicotinic alpha 2 subunit
Acc ID: DOID:0081119
Term: benign familial infantile seizures 6
Definition: A benign familial infantile epilepsy that is characterized by afebrile partial complex or generalized tonic-clonic seizures occurring between 3 and 12 months of age with a good response to medication and no neurologic sequelae and that has_material_basis_in mutation in the CHRNA2 gene on chromosome 8p21. (DO)
Definition Source(s): https://pubmed.ncbi.nlm.nih.gov/25847220/ "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)
Chrna2 ISOCHRNA2 (Homo sapiens)7240710OMIM  
Chrna2 ISOCHRNA2 (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Autosomal dominant nocturnal frontal lobe epilepsyPMID:16199547 PMID:17576681 PMID:18414213 PMID:21703448 PMID:24950454 PMID:25741868 PMID:25847220 PMID:26467025 PMID:28166811 PMID:28492532 PMID:9536098
Chrna2 ISOCHRNA2 (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Autosomal dominant nocturnal frontal lobe epilepsy | ClinVar Annotator: match by term: Seizures, benign familial infantile, 6PMID:16199547 PMID:16826524 PMID:17576681 PMID:18414213 PMID:24950454 PMID:25741868 PMID:25847220 PMID:26467025 PMID:28166811 PMID:28492532 PMID:29930392 PMID:9536098
Go Back to source page   Continue to Ontology report