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GENE - TERM ANNOTATION REPORT

RGD ID: 621657
Species: Rattus norvegicus
RGD Object: Gene
Symbol: Scn3b
Name: sodium voltage-gated channel beta subunit 3
Acc ID: DOID:0110224
Term: Brugada syndrome 7
Definition: A Brugada syndrome that has_material_basis_in heterozygous mutation in the SCN3B gene on chromosome 11q24. (DO)
Definition Source(s): https://www.ncbi.nlm.nih.gov/pubmed/20031595 "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)
Scn3b ISOSCN3B (Homo sapiens)7240710OMIM  
Scn3b ISOSCN3B (Homo sapiens)11554173CTDCTD Direct Evidence: marker/mechanism 
Scn3b ISOSCN3B (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Atrial fibrillation, familial, 16 | ClinVar Annotator: match by term: Brugada syndrome 7PMID:16199547 PMID:17576681 PMID:20031595 PMID:20042427 PMID:20226894 PMID:20558140 PMID:21051419 PMID:22284586 PMID:23257389 PMID:23414114 PMID:23861362 PMID:24033266 PMID:24055113 PMID:24144883 PMID:24529773 PMID:25650408 PMID:25741868 PMID:25757662 PMID:26179811 PMID:27435932 PMID:27711072 PMID:28166811 PMID:28492532 PMID:29247119 PMID:30662450 PMID:30821013 PMID:30847666 PMID:31019283 PMID:31043699 PMID:9536098
Scn3b ISSScn3b (Mus musculus)13592920MouseDOOMIM:613120 
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