Gene: UCN ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 7349
Gene Symbol: UCN
UCN 		0.010 GeneticVariation disease BEFREE Monomelic amyotrophy associated with the 7472insC mutation in the mtDNA tRNASer(UCN) gene. 15482956 2004