Gene: TPP1 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1200
Gene Symbol: TPP1
TPP1 		0.020 GeneticVariation group BEFREE Our findings document that late infantile neuronal ceroid lipofuscinosis (CLN2), which is caused by TPP1 gene mutations, should be considered in the differential diagnosis of autosomal recessive dystonia-parkinsonism syndromes. 26143525 2015
Entrez Id: 1200
Gene Symbol: TPP1
TPP1 		0.020 GeneticVariation group BEFREE A CLN2 gene nonsense mutation is associated with severe caudate atrophy and dystonia in LINCL. 11071145 2000