Gene: RTN2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6253
Gene Symbol: RTN2
RTN2 		0.010 Biomarker disease BEFREE Mutations in the ER-shaping protein reticulon 2 cause the axon-degenerative disorder hereditary spastic paraplegia type 12. 22232211 2012