Gene: FSCN2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 25794
Gene Symbol: FSCN2
FSCN2 		0.220 GeneticVariation disease BEFREE Sequence variations in the retinal fascin FSCN2 gene in a Spanish population with autosomal dominant retinitis pigmentosa or macular degeneration. 16280978 2005
Entrez Id: 25794
Gene Symbol: FSCN2
FSCN2 		0.220 Biomarker disease MGD Targeted disruption of FSCN2 gene induces retinopathy in mice. 16043865 2005
Entrez Id: 25794
Gene Symbol: FSCN2
FSCN2 		0.220 GeneticVariation disease BEFREE Autosomal dominant macular degeneration associated with 208delG mutation in the FSCN2 gene. 14609921 2003