Source: CLINGEN

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6323
Gene Symbol: SCN1A
SCN1A
CUI: C1864987
Disease: Migraine, Familial Hemiplegic, 3
Migraine, Familial Hemiplegic, 3 		0.700 Biomarker CLINGEN Two novel families with hemiplegic migraine caused by recurrent SCN1A mutation p.F1499L. 29145747

2018
Entrez Id: 6323
Gene Symbol: SCN1A
SCN1A
CUI: C1864987
Disease: Migraine, Familial Hemiplegic, 3
Migraine, Familial Hemiplegic, 3 		0.700 Biomarker CLINGEN Familial Hemiplegic Migraine Type 3 (FHM3) With an SCN1A Mutation in a Chinese Family: A Case Report. 30498473

2018
Entrez Id: 6323
Gene Symbol: SCN1A
SCN1A
CUI: C1864987
Disease: Migraine, Familial Hemiplegic, 3
Migraine, Familial Hemiplegic, 3 		0.700 Biomarker CLINGEN Gain of Function for the SCN1A/hNav1.1-L1670W Mutation Responsible for Familial Hemiplegic Migraine. 30038559

2018
Entrez Id: 6323
Gene Symbol: SCN1A
SCN1A
CUI: C1864987
Disease: Migraine, Familial Hemiplegic, 3
Migraine, Familial Hemiplegic, 3 		0.700 Biomarker CLINGEN A novel SCN1A mutation identified in a Chinese family with familial hemiplegic migraine: A case report. 27919014

2017
Entrez Id: 6323
Gene Symbol: SCN1A
SCN1A
CUI: C1864987
Disease: Migraine, Familial Hemiplegic, 3
Migraine, Familial Hemiplegic, 3 		0.700 Biomarker CLINGEN Early-onset familial hemiplegic migraine due to a novel SCN1A mutation. 26763045

2016
Entrez Id: 6323
Gene Symbol: SCN1A
SCN1A
CUI: C1864987
Disease: Migraine, Familial Hemiplegic, 3
Migraine, Familial Hemiplegic, 3 		0.700 Biomarker CLINGEN Clinical and electroencephalographic abnormalities during the full duration of a sporadic hemiplegic migraine attack. 27155821

2016
Entrez Id: 6323
Gene Symbol: SCN1A
SCN1A
CUI: C1864987
Disease: Migraine, Familial Hemiplegic, 3
Migraine, Familial Hemiplegic, 3 		0.700 Biomarker CLINGEN Genetic studies of Polish migraine patients: screening for causative mutations in four migraine-associated genes. 26747084

2016
Entrez Id: 6323
Gene Symbol: SCN1A
SCN1A
CUI: C1864987
Disease: Migraine, Familial Hemiplegic, 3
Migraine, Familial Hemiplegic, 3 		0.700 Biomarker CLINGEN Familial hemiplegic migraine due to L263V SCN1A mutation: discordance for epilepsy between two kindreds from Douro Valley. 24646837

2014
Entrez Id: 6323
Gene Symbol: SCN1A
SCN1A
CUI: C1864987
Disease: Migraine, Familial Hemiplegic, 3
Migraine, Familial Hemiplegic, 3 		0.700 Biomarker CLINGEN Two novel SCN1A mutations identified in families with familial hemiplegic migraine. 24707016

2014
Entrez Id: 6323
Gene Symbol: SCN1A
SCN1A
CUI: C1864987
Disease: Migraine, Familial Hemiplegic, 3
Migraine, Familial Hemiplegic, 3 		0.700 Biomarker CLINGEN First mutation in the voltage-gated Nav1.1 subunit gene SCN1A with co-occurring familial hemiplegic migraine and epilepsy. 19220312

2009
Entrez Id: 6323
Gene Symbol: SCN1A
SCN1A
CUI: C1864987
Disease: Migraine, Familial Hemiplegic, 3
Migraine, Familial Hemiplegic, 3 		0.700 Biomarker CLINGEN Elicited repetitive daily blindness: a new phenotype associated with hemiplegic migraine and SCN1A mutations. 19332696

2009
Entrez Id: 6323
Gene Symbol: SCN1A
SCN1A
CUI: C1864987
Disease: Migraine, Familial Hemiplegic, 3
Migraine, Familial Hemiplegic, 3 		0.700 Biomarker CLINGEN Self-limited hyperexcitability: functional effect of a familial hemiplegic migraine mutation of the Nav1.1 (SCN1A) Na+ channel. 18632931

2008
Entrez Id: 6323
Gene Symbol: SCN1A
SCN1A
CUI: C1864987
Disease: Migraine, Familial Hemiplegic, 3
Migraine, Familial Hemiplegic, 3 		0.700 Biomarker CLINGEN Novel mutation confirms seizure locus SCN1A is also familial hemiplegic migraine locus FHM3. 18021921

2007
Entrez Id: 6323
Gene Symbol: SCN1A
SCN1A
CUI: C1864987
Disease: Migraine, Familial Hemiplegic, 3
Migraine, Familial Hemiplegic, 3 		0.700 Biomarker CLINGEN The novel p.L1649Q mutation in the SCN1A epilepsy gene is associated with familial hemiplegic migraine: genetic and functional studies. Mutation in brief #957. Online. 17397047

2007
Entrez Id: 6323
Gene Symbol: SCN1A
SCN1A
CUI: C1864987
Disease: Migraine, Familial Hemiplegic, 3
Migraine, Familial Hemiplegic, 3 		0.700 Biomarker CLINGEN Nav1.1 localizes to axons of parvalbumin-positive inhibitory interneurons: a circuit basis for epileptic seizures in mice carrying an Scn1a gene mutation. 17537961

2007
Entrez Id: 6323
Gene Symbol: SCN1A
SCN1A
CUI: C1864987
Disease: Migraine, Familial Hemiplegic, 3
Migraine, Familial Hemiplegic, 3 		0.700 Biomarker CLINGEN Mutation in the neuronal voltage-gated sodium channel SCN1A in familial hemiplegic migraine. 16054936

2005