Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6513
Gene Symbol: SLC2A1
SLC2A1 		0.710 Biomarker disease GENOMICS_ENGLAND A 23 years follow-up study identifies GLUT1 deficiency syndrome initially diagnosed as complicated hereditary spastic paraplegia. 27725288 2016
Entrez Id: 6513
Gene Symbol: SLC2A1
SLC2A1 		0.710 CausalMutation disease CLINVAR Clinical utility of genetic testing in pediatric drug-resistant epilepsy: a pilot study. 25108116 2014
Entrez Id: 6513
Gene Symbol: SLC2A1
SLC2A1 		0.710 Biomarker disease BEFREE This study shows that DYT9 and DYT18 are allelic disorders and enlarges the spectrum of GLUT1 phenotypes, now also including slowly progressive spastic paraparesis combined with PED. 21832227 2011
Entrez Id: 6513
Gene Symbol: SLC2A1
SLC2A1 		0.710 Biomarker disease GENOMICS_ENGLAND This study shows that DYT9 and DYT18 are allelic disorders and enlarges the spectrum of GLUT1 phenotypes, now also including slowly progressive spastic paraparesis combined with PED. 21832227 2011
Entrez Id: 6513
Gene Symbol: SLC2A1
SLC2A1 		0.710 GermlineCausalMutation disease ORPHANET This study shows that DYT9 and DYT18 are allelic disorders and enlarges the spectrum of GLUT1 phenotypes, now also including slowly progressive spastic paraparesis combined with PED. 21832227 2011
Entrez Id: 6513
Gene Symbol: SLC2A1
SLC2A1 		0.710 GeneticVariation disease UNIPROT This study shows that DYT9 and DYT18 are allelic disorders and enlarges the spectrum of GLUT1 phenotypes, now also including slowly progressive spastic paraparesis combined with PED. 21832227 2011
Entrez Id: 6513
Gene Symbol: SLC2A1
SLC2A1 		0.710 Biomarker disease GENOMICS_ENGLAND Paroxysmal exercise-induced dyskinesia and epilepsy is due to mutations in SLC2A1, encoding the glucose transporter GLUT1. 18577546 2008
Entrez Id: 6513
Gene Symbol: SLC2A1
SLC2A1 		0.710 Biomarker disease CTD_human
Entrez Id: 6513
Gene Symbol: SLC2A1
SLC2A1 		0.710 GeneticVariation disease CLINVAR