Gene: CYP7B1 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 9420
Gene Symbol: CYP7B1
CYP7B1 		0.320 GeneticVariation disease BEFREE The frequency of CYP7B1 mutations were 7.3% (n = 6/82) in our series of autosomal recessive hereditary spastic paraplegia families and 3.3% (n = 3/90) in our series of sporadic pure spastic paraplegia. 19439420 2009
Entrez Id: 9420
Gene Symbol: CYP7B1
CYP7B1 		0.320 Biomarker disease CTD_human Sequence alterations within CYP7B1 implicate defective cholesterol homeostasis in motor-neuron degeneration. 18252231 2008
Entrez Id: 9420
Gene Symbol: CYP7B1
CYP7B1 		0.320 Biomarker disease BEFREE A clinical and genetic study of SPG5A linked autosomal recessive hereditary spastic paraplegia. 12874406 2003