Gene: SLC2A1 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6513
Gene Symbol: SLC2A1
SLC2A1 		0.040 GeneticVariation disease BEFREE A novel SLC2A1 mutation linking hemiplegic migraine with alternating hemiplegia of childhood. 24824604 2015
Entrez Id: 6513
Gene Symbol: SLC2A1
SLC2A1 		0.040 GeneticVariation disease BEFREE Alternating hemiplegia of childhood with a de novo mutation in ATP1A3 and changes in SLC2A1 responsive to a ketogenic diet. 24491413 2014
Entrez Id: 6513
Gene Symbol: SLC2A1
SLC2A1 		0.040 GeneticVariation disease BEFREE Lack of SLC2A1 (glucose transporter 1) mutations in 30 Italian patients with alternating hemiplegia of childhood. 22899793 2013
Entrez Id: 6513
Gene Symbol: SLC2A1
SLC2A1 		0.040 GeneticVariation disease BEFREE Absence of mutation in the SLC2A1 gene in a cohort of patients with alternating hemiplegia of childhood (AHC). 21445818 2010