Gene: SPG7 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6687
Gene Symbol: SPG7
SPG7 		0.430 GeneticVariation disease BEFREE SPG7 mutational screening in spastic paraplegia patients supports a dominant effect for some mutations and a pathogenic role for p.A510V. 22571692 2013
Entrez Id: 6687
Gene Symbol: SPG7
SPG7 		0.430 GeneticVariation disease BEFREE The identification of SPG7 as the gene defective in a recessive form of spastic paraplegia has drawn attention to the yeast protein family of ATP-dependent zinc metalloproteases. 11549317 2001
Entrez Id: 6687
Gene Symbol: SPG7
SPG7 		0.430 Biomarker disease CTD_human The identification of SPG7 as the gene defective in a recessive form of spastic paraplegia has drawn attention to the yeast protein family of ATP-dependent zinc metalloproteases. 11549317 2001
Entrez Id: 6687
Gene Symbol: SPG7
SPG7 		0.430 GeneticVariation disease BEFREE Spastic paraplegia and OXPHOS impairment caused by mutations in paraplegin, a nuclear-encoded mitochondrial metalloprotease. 9635427 1998
Entrez Id: 6687
Gene Symbol: SPG7
SPG7 		0.430 CausalMutation disease CLINVAR
Entrez Id: 6687
Gene Symbol: SPG7
SPG7 		0.430 Biomarker disease HPO