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GENE - TERM ANNOTATION REPORT

RGD ID: 3632
Species: Rattus norvegicus
RGD Object: Gene
Symbol: Scn2a
Name: sodium voltage-gated channel alpha subunit 2
Acc ID: DOID:630
Term: genetic disease
Definition: A disease that has_material_basis_in genetic variations in the human genome. (DO)
Definition Source(s): http://ghr.nlm.nih.gov/ "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)
Scn2a ISOSCN2A (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:11371648 PMID:11738931 PMID:12037327 PMID:12620097 PMID:15048894 PMID:15301839 PMID:16122630 PMID:17576681 PMID:18414213 PMID:19702560 PMID:19783390 PMID:19786696 PMID:20869590 PMID:20956790 PMID:21439835 PMID:22029951 PMID:22495306 PMID:22581653 PMID:22591750 PMID:23020937 PMID:23195492 PMID:23603762 PMID:23708187 PMID:23849776 PMID:23935176 PMID:24579881 PMID:24650168 PMID:25131622 PMID:25156649 PMID:25326637 PMID:25473036 PMID:25741868 PMID:25818041 PMID:25937001 PMID:26291284 PMID:26467025 PMID:26555645 PMID:26645390 PMID:26680202 PMID:26689363 PMID:26993267 PMID:27328862 PMID:27353043 PMID:27824329 PMID:28087622 PMID:28096396 PMID:28150151 PMID:28183995 PMID:28191889 PMID:28256214 PMID:28263302 PMID:28379373 PMID:28492532 PMID:28518218 PMID:28735751 PMID:28947817 PMID:29100083 PMID:29691040 PMID:29852413 PMID:30415926 PMID:30564305 PMID:30619928 PMID:31054490 PMID:31302675 PMID:32090326 PMID:32400968 PMID:32845893 PMID:33000761 PMID:33004838 PMID:34156984 PMID:34469436 PMID:35715422 PMID:37578743 PMID:9536098
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