Gene: NT5C2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 22978
Gene Symbol: NT5C2
NT5C2 		0.010 GeneticVariation disease BEFREE Novel homozygous missense mutation in NT5C2 underlying hereditary spastic paraplegia SPG45. 28884889 2017