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 		0.110 GeneticVariation disease BEFREE In conclusion, these data confirm the presence of SPG10 (chromosome 12), potentially reduce the minimum candidate region for SPG12 (chromosome 19q), and suggest there is at least one additional autosomal dominant SPG locus. 11354831 2001
Entrez Id: 6253
Gene Symbol: RTN2
RTN2 		0.110 Biomarker disease HPO