Gene: MCF2L ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 23263
Gene Symbol: MCF2L
MCF2L 		0.010 GeneticVariation disease BEFREE These findings also contribute structural information to understand mutations in human 6-OST isoform 1 associated with the human genetic disease idiopathic hypogonadotropic hypogonadism characterized by incomplete or lack of puberty. 28103688 2017