AANAT, aralkylamine N-acetyltransferase, 15

N. diseases: 36; N. variants: 8
Disease: Melatonin deficiency ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4285716
Disease: Melatonin deficiency
Melatonin deficiency 		0.010 GeneticVariation disease BEFREE Melatonin deficiency in this strain results from nonfunctional alleles of the genes coding 2 key enzymes of the melatonin synthesis pathway: arylalkylamine-N-acetyltransferase (Aanat) and N-acetylserotonin-O-methyltransferase (Asmt). 29768727 2018