Gene: TMPRSS3 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 64699
Gene Symbol: TMPRSS3
TMPRSS3 		0.060 GeneticVariation disease BEFREE Mutations in the gene cause non-syndromic autosomal recessive deafness (DFNB8/10) in humans. 29460002 2018
Entrez Id: 64699
Gene Symbol: TMPRSS3
TMPRSS3 		0.060 GeneticVariation disease BEFREE Mutations in the type II transmembrane serine protease 3 (TMPRSS3) gene cause non-syndromic autosomal recessive deafness (DFNB8/10), characterized by congenital or childhood onset bilateral profound hearing loss. 21454591 2011
Entrez Id: 64699
Gene Symbol: TMPRSS3
TMPRSS3 		0.060 GeneticVariation disease BEFREE TMPRSS3, a type II transmembrane serine protease mutated in non-syndromic autosomal recessive deafness. 17981648 2008
Entrez Id: 64699
Gene Symbol: TMPRSS3
TMPRSS3 		0.060 GeneticVariation disease BEFREE TMPRSS3 encodes a transmembrane serine protease that contains both LDLRA and SRCR domains and is mutated in non-syndromic autosomal recessive deafness (DFNB8/10). 12393794 2002
Entrez Id: 64699
Gene Symbol: TMPRSS3
TMPRSS3 		0.060 GeneticVariation disease BEFREE Novel missense mutations of TMPRSS3 in two consanguineous Tunisian families with non-syndromic autosomal recessive deafness. 11462234 2001
Entrez Id: 64699
Gene Symbol: TMPRSS3
TMPRSS3 		0.060 Biomarker disease BEFREE This chromosomal region is known to contain genes for human diseases such as non-syndromic autosomal recessive deafness (DFNB8/10) and autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED). 9325172 1997