Gene: SPG11 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 80208
Gene Symbol: SPG11
SPG11 		0.400 GeneticVariation disease LHGDN SPG11 mutations are common in familial cases of complicated hereditary spastic paraplegia. 18337587 2008
Entrez Id: 80208
Gene Symbol: SPG11
SPG11 		0.400 GeneticVariation disease LHGDN Two novel mutations in the SPG11 gene causing hereditary spastic paraplegia associated with thin corpus callosum. 18361476 2008
Entrez Id: 80208
Gene Symbol: SPG11
SPG11 		0.400 GeneticVariation disease BEFREE Novel mutations of the SPG11 gene in hereditary spastic paraplegia with thin corpus callosum. 18835492 2008
Entrez Id: 80208
Gene Symbol: SPG11
SPG11 		0.400 GeneticVariation disease BEFREE We conclude that mutations on KIAA1840 are frequent in complex autosomal recessive hereditary spastic paraplegia but an infrequent cause of sporadic complex hereditary spastic paraplegia. 18337587 2008
Entrez Id: 80208
Gene Symbol: SPG11
SPG11 		0.400 GeneticVariation disease LHGDN Clinical heterogeneity and genotype-phenotype correlations in hereditary spastic paraplegia because of Spatacsin mutations (SPG11). 18717728 2008
Entrez Id: 80208
Gene Symbol: SPG11
SPG11 		0.400 GeneticVariation disease LHGDN Long-term course and mutational spectrum of spatacsin-linked spastic paraplegia. 18067136 2007
Entrez Id: 80208
Gene Symbol: SPG11
SPG11 		0.400 Biomarker disease BEFREE Further clinical and genetic characterization of SPG11: hereditary spastic paraplegia with thin corpus callosum. 16773502 2006
Entrez Id: 80208
Gene Symbol: SPG11
SPG11 		0.400 GeneticVariation disease BEFREE Clinical progression and genetic analysis in hereditary spastic paraplegia with thin corpus callosum in spastic gait gene 11 (SPG11). 14732628 2004