rs3205493, EIF3K

N. diseases: 1
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Amyotrophic Lateral Sclerosis
CUI: C0002736
Disease: Amyotrophic Lateral Sclerosis
0.030 GeneticVariation BEFREE We also show that myofibers with dynein impairment or from an amyotrophic lateral sclerosis (ALS) model (SOD1(G93A)) show similar defects in myofiber formation and agrin-induced AChR clustering suggesting a role for dynein impairment in ALS progression. 27283349 2016
Amyotrophic Lateral Sclerosis
CUI: C0002736
Disease: Amyotrophic Lateral Sclerosis
0.030 GeneticVariation BEFREE Progressive motor unit loss in the G93A mouse model of amyotrophic lateral sclerosis is unaffected by gender. 19208415 2009
Amyotrophic Lateral Sclerosis
CUI: C0002736
Disease: Amyotrophic Lateral Sclerosis
0.030 GeneticVariation BEFREE Time course of preferential motor unit loss in the SOD1 G93A mouse model of amyotrophic lateral sclerosis. 17766128 2007