Gene: GSN ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2934
Gene Symbol: GSN
GSN 		0.130 Biomarker disease BEFREE The accumulation of amyloid fibrils with severe elastolysis characterises both dermal and vascular derangement in AGel amyloidosis. 31814469 2019
Entrez Id: 2934
Gene Symbol: GSN
GSN 		0.130 GeneticVariation disease BEFREE Patients with hereditary gelsolin (AGel) amyloidosis (HGA) present with hanging skin (cutis laxa) and bilateral cranial neuropathy, and require symptomatic plastic surgery. 27879149 2016
Entrez Id: 2934
Gene Symbol: GSN
GSN 		0.130 GeneticVariation disease BEFREE AGel amyloidosis caused by a gelsolin G654A gene mutation is autosomally dominantly inherited and presents typically in the 30s with progressive corneal lattice dystrophy, followed by cutis laxa and cranial polyneuropathy. 19701715 2009
Entrez Id: 2934
Gene Symbol: GSN
GSN 		0.130 Biomarker disease HPO