Gene: SMG7 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 9887
Gene Symbol: SMG7
SMG7 		0.100 GeneticVariation disease CLINVAR Two CGD Families with a Hypomorphic Mutation in the Activation Domain of p67phox. 25937994 2014
Entrez Id: 9887
Gene Symbol: SMG7
SMG7 		0.100 GeneticVariation disease CLINVAR Hematologically important mutations: the autosomal recessive forms of chronic granulomatous disease (second update). 20167518 2010
Entrez Id: 9887
Gene Symbol: SMG7
SMG7 		0.100 GeneticVariation disease CLINVAR Four different NCF2 mutations in six families from Turkey and an overview of NCF2 gene mutations. 19624736 2009
Entrez Id: 9887
Gene Symbol: SMG7
SMG7 		0.100 GeneticVariation disease CLINVAR Focus on FOCIS: the continuing diagnostic challenge of autosomal recessive chronic granulomatous disease. 18625437 2008
Entrez Id: 9887
Gene Symbol: SMG7
SMG7 		0.100 GeneticVariation disease CLINVAR Molecular characterization of autosomal recessive chronic granulomatous disease caused by a defect of the nicotinamide adenine dinucleotide phosphate (reduced form) oxidase component p67-phox. 10498624 1999
Entrez Id: 9887
Gene Symbol: SMG7
SMG7 		0.100 GeneticVariation disease CLINVAR Autosomal recessive chronic granulomatous disease caused by novel mutations in NCF-2, the gene encoding the p67-phox component of phagocyte NADPH oxidase. 10598813 1999
Entrez Id: 9887
Gene Symbol: SMG7
SMG7 		0.100 CausalMutation disease CLINVAR