Gene: CNTF ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1270
Gene Symbol: CNTF
CNTF 		0.320 Biomarker disease CTD_human Early onset of severe familial amyotrophic lateral sclerosis with a SOD-1 mutation: potential impact of CNTF as a candidate modifier gene. 11951178 2002
Entrez Id: 1270
Gene Symbol: CNTF
CNTF 		0.320 GeneticVariation disease BEFREE Early onset of severe familial amyotrophic lateral sclerosis with a SOD-1 mutation: potential impact of CNTF as a candidate modifier gene. 11951178 2002
Entrez Id: 1270
Gene Symbol: CNTF
CNTF 		0.320 GeneticVariation disease BEFREE Investigation of a null mutation of the CNTF gene in familial amyotrophic lateral sclerosis. 8543936 1995