Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 123606
Gene Symbol: NIPA1
NIPA1
0.010 GeneticVariation phenotype BEFREE Mutations in the NIPA1(SPG6) gene, named for "nonimprinted in Prader-Willi/Angelman" has been implicated in one form of autosomal dominant hereditary spastic paraplegia (HSP), a neurodegenerative disorder characterized by progressive lower limb spasticity and weakness. 17166836 2007