Gene: MARVELD2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 153562
Gene Symbol: MARVELD2
MARVELD2 		0.340 Biomarker disease CLINGEN Spectrum of DNA variants for non-syndromic deafness in a large cohort from multiple continents. 27344577 2016
Entrez Id: 153562
Gene Symbol: MARVELD2
MARVELD2 		0.340 GeneticVariation disease BEFREE Recessive mutations of TRIC (DFNB49) encoding tricellulin and ILDR1 (DFNB42) cause human nonsyndromic deafness. 25217574 2015
Entrez Id: 153562
Gene Symbol: MARVELD2
MARVELD2 		0.340 Biomarker disease CLINGEN Deletion of Tricellulin Causes Progressive Hearing Loss Associated with Degeneration of Cochlear Hair Cells. 26677943 2015
Entrez Id: 153562
Gene Symbol: MARVELD2
MARVELD2 		0.340 Biomarker disease CLINGEN Deafness in occludin-deficient mice with dislocation of tricellulin and progressive apoptosis of the hair cells. 25063198 2014
Entrez Id: 153562
Gene Symbol: MARVELD2
MARVELD2 		0.340 Biomarker disease CLINGEN Mutations in TRIC (also known as MARVELD2), which encodes a tricellular tight junction protein known as tricellulin, lead to nonsyndromic hearing loss (DFNB49). 23979167 2013
Entrez Id: 153562
Gene Symbol: MARVELD2
MARVELD2 		0.340 Biomarker disease CLINGEN A comprehensive study to determine heterogeneity of autosomal recessive nonsyndromic hearing loss in Iran. 22903915 2012
Entrez Id: 153562
Gene Symbol: MARVELD2
MARVELD2 		0.340 Biomarker disease CLINGEN Splice-site mutations in the TRIC gene underlie autosomal recessive nonsyndromic hearing impairment in Pakistani families. 18084694 2008
Entrez Id: 153562
Gene Symbol: MARVELD2
MARVELD2 		0.340 GeneticVariation disease BEFREE Splice-site mutations in the TRIC gene underlie autosomal recessive nonsyndromic hearing impairment in Pakistani families. 18084694 2008
Entrez Id: 153562
Gene Symbol: MARVELD2
MARVELD2 		0.340 GeneticVariation disease BEFREE We show that, in humans, four different recessive mutations of TRIC cause nonsyndromic deafness (DFNB49), a surprisingly limited phenotype, given the widespread tissue distribution of tricellulin in epithelial cells. 17186462 2006
Entrez Id: 153562
Gene Symbol: MARVELD2
MARVELD2 		0.340 Biomarker disease CLINGEN We show that, in humans, four different recessive mutations of TRIC cause nonsyndromic deafness (DFNB49), a surprisingly limited phenotype, given the widespread tissue distribution of tricellulin in epithelial cells. 17186462 2006
Entrez Id: 153562
Gene Symbol: MARVELD2
MARVELD2 		0.340 GeneticVariation disease BEFREE The mapping of DFNB49 further confirms the heterogeneity underlying autosomal recessive forms of nonsyndromic deafness. 15538632 2005