Gene: NINJ1 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4814
Gene Symbol: NINJ1
NINJ1 		0.020 GeneticVariation disease BEFREE Our results rule out a mutation in the translated region of the ninjurin gene as a cause of HSN type I and type II. 10232753 1999
Entrez Id: 4814
Gene Symbol: NINJ1
NINJ1 		0.020 GeneticVariation disease BEFREE The human homologue of the ninjurin gene maps to the candidate region of hereditary sensory neuropathy type I (HSNI). 9465296 1998