Gene: SPG16 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 57760
Gene Symbol: SPG16
SPG16 		0.020 GeneticVariation disease BEFREE NT5C2 novel splicing variant expands the phenotypic spectrum of Spastic Paraplegia (SPG45): case report of a new member of thin corpus callosum SPG-Subgroup. 28327087 2017
Entrez Id: 57760
Gene Symbol: SPG16
SPG16 		0.020 Biomarker disease BEFREE Familial spastic paraplegia (FSP or SPG) is a genetically heterogeneous group of upper motor neuron syndromes. 8782167 1996