Gene: MOB3B ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 79817
Gene Symbol: MOB3B
MOB3B 		0.110 GeneticVariation disease GWASCAT Second-generation Irish genome-wide association study for amyotrophic lateral sclerosis. 25442119 2015
Entrez Id: 79817
Gene Symbol: MOB3B
MOB3B 		0.110 Biomarker disease BEFREE Rare variants in the coding region of UNC13a, IFNK, MOBKL2b, and C9ORF72 are unlikely to be a genetic cause of ALS. 23141412 2013
Entrez Id: 79817
Gene Symbol: MOB3B
MOB3B 		0.110 GeneticVariation disease GWASDB Residual association at C9orf72 suggests an alternative amyotrophic lateral sclerosis-causing hexanucleotide repeat. 23587638 2013
Entrez Id: 79817
Gene Symbol: MOB3B
MOB3B 		0.110 GeneticVariation disease GWASDB Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study. 20801718 2010
Entrez Id: 79817
Gene Symbol: MOB3B
MOB3B 		0.110 GeneticVariation disease GWASDB Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study. 20801717 2010