Gene: NMNAT1 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 64802
Gene Symbol: NMNAT1
NMNAT1 		0.500 Biomarker phenotype CTD_human Mutations in NMNAT1 cause Leber congenital amaurosis and identify a new disease pathway for retinal degeneration. 22842230 2012
Entrez Id: 64802
Gene Symbol: NMNAT1
NMNAT1 		0.500 Biomarker phenotype MGD