STX17, syntaxin 17, 55014

N. diseases: 11; N. variants: 1
Disease: melanoma ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0025202
Disease: melanoma
melanoma 		0.320 GeneticVariation disease BEFREE The Grey phenotype in horses, caused by a 4.6 kb duplication in intron 6 of Syntaxin 17 (STX17), is associated with a very high incidence of cutaneous melanoma, but the molecular mechanism behind the melanomagenesis remains unknown. 25413220 2014
CUI: C0025202
Disease: melanoma
melanoma 		0.320 GeneticVariation disease BEFREE We conclude that common variants in the STX17 gene region do not play a key role in the pathogenesis of human melanoma. 19209086 2009
CUI: C0025202
Disease: melanoma
melanoma 		0.320 Biomarker disease CTD_human Both STX17 and the neighboring NR4A3 gene are overexpressed in melanomas from Gray horses. 18641652 2008