Source: BEFREE

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 8910
Gene Symbol: SGCE
SGCE
CUI: C0752203
Disease: Dystonia, Primary
Dystonia, Primary 		0.020 GeneticVariation BEFREE Furthermore, torsinA, that is mutated in DYT1 dystonia, a rare type of primary dystonia, binds to and promotes the degradation of epsilon-sarcoglycan mutants when both proteins are co-expressed. 17200151

2007
Entrez Id: 8910
Gene Symbol: SGCE
SGCE
CUI: C0752203
Disease: Dystonia, Primary
Dystonia, Primary 		0.020 GeneticVariation BEFREE Our results suggest that mutations in the SGCE gene cannot be held responsible for other subtypes of primary dystonia. 15390016

2004