Gene: DUOX2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 50506
Gene Symbol: DUOX2
DUOX2 		0.150 GeneticVariation disease BEFREE Double variants in TSHR and DUOX2 in a patient with hypothyroidism: case report. 31541602 2019
Entrez Id: 50506
Gene Symbol: DUOX2
DUOX2 		0.150 GeneticVariation disease BEFREE Genotypes and phenotypes of congenital goitre and hypothyroidism caused by mutations in dual oxidase 2 genes. 24735383 2014
Entrez Id: 50506
Gene Symbol: DUOX2
DUOX2 		0.150 GeneticVariation disease BEFREE Mutation of either DUOX2 or DUOXA2 gene is a newly recognized cause of hypothyroidism due to insufficient H(2)O(2) production. 20407074 2010
Entrez Id: 50506
Gene Symbol: DUOX2
DUOX2 		0.150 GeneticVariation disease BEFREE Novel missense and splice-site DUOX2 mutations in compound heterozygosity have been recently reported in association with a wide spectrum of hypothyroid phenotypes, ranging from very mild to severe. 17684392 2007
Entrez Id: 50506
Gene Symbol: DUOX2
DUOX2 		0.150 GeneticVariation disease BEFREE In conclusion, we report two novel sequence variants in DUOX2 gene that are associated with persistent mild hypothyroidism and PIOD in two siblings. 16134168 2005
Entrez Id: 50506
Gene Symbol: DUOX2
DUOX2 		0.150 Biomarker disease HPO