Disease: Motor Neuron Disease ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs137852972
rs137852972
Entrez Id: 26580;100534595
Gene Symbol: BSCL2;HNRNPUL2-BSCL2
BSCL2;HNRNPUL2-BSCL2
CUI: C0085084
Disease:
Motor Neuron Disease 		0.020 GeneticVariation BEFREE N88S seipin mutant transgenic mice develop features of seipinopathy/BSCL2-related motor neuron disease via endoplasmic reticulum stress. 21750110 2011
dbSNP: rs137852972
rs137852972
Entrez Id: 26580;100534595
Gene Symbol: BSCL2;HNRNPUL2-BSCL2
BSCL2;HNRNPUL2-BSCL2
CUI: C0085084
Disease:
Motor Neuron Disease 		0.020 GeneticVariation BEFREE Recently, gain-of-toxic-function mutations (namely, mutations N88S and S90L) in the seipin gene have been identified in autosomal dominant motor neuron diseases such as Silver syndrome/spastic paraplegia 17 (SPG17) (OMIM #270685) and distal hereditary motor neuropathy type V (dHMN-V) (OMIM #182960). 18790819 2009