Gene: DECR1 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1666
Gene Symbol: DECR1
DECR1 		0.020 GeneticVariation disease BEFREE A novel missense mutation (I26M) in DUOXA2 causing congenital goiter hypothyroidism impairs NADPH oxidase activity but not protein expression. 25675383 2015
Entrez Id: 1666
Gene Symbol: DECR1
DECR1 		0.020 GeneticVariation disease BEFREE Hypothyroidism-associated missense mutation impairs NADPH oxidase activity and intracellular trafficking of Duox2. 24853759 2014