Gene: TRNL1 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4567
Gene Symbol: TRNL1
TRNL1 		0.010 GeneticVariation disease BEFREE The m.3243A>G MTTL1 mutation is the most common cause of mitochondrial disease; yet there is limited awareness of intestinal pseudo-obstruction (IPO) in this disorder. 27453452 2016