Gene: GNAT2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2780
Gene Symbol: GNAT2
GNAT2 		0.120 GeneticVariation disease BEFREE Variant phenotypes of incomplete achromatopsia in two cousins with GNAT2 gene mutations. 15557429 2004
Entrez Id: 2780
Gene Symbol: GNAT2
GNAT2 		0.120 GeneticVariation disease BEFREE Since mutations in the CNGA3 gene may cause a variety of retinal dystrophies (complete and incomplete achromatopsia and progressive cone dystrophy), GNAT2 mutations may also prove to be implicated in other forms of retinal dystrophy with cone dysfunction. 12205108 2002
Entrez Id: 2780
Gene Symbol: GNAT2
GNAT2 		0.120 Biomarker disease HPO