Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 286676
Gene Symbol: ILDR1
ILDR1 		0.900 Biomarker disease MGD ILDR1 null mice, a model of human deafness DFNB42, show structural aberrations of tricellular tight junctions and degeneration of auditory hair cells. 25217574 2015
Entrez Id: 286676
Gene Symbol: ILDR1
ILDR1 		0.900 Biomarker disease MGD Deficiency of angulin-2/ILDR1, a tricellular tight junction-associated membrane protein, causes deafness with cochlear hair cell degeneration in mice. 25822906 2015
Entrez Id: 286676
Gene Symbol: ILDR1
ILDR1 		0.900 Biomarker disease MGD ILDR1 deficiency causes degeneration of cochlear outer hair cells and disrupts the structure of the organ of Corti: a mouse model for human DFNB42. 25819842 2015
Entrez Id: 286676
Gene Symbol: ILDR1
ILDR1 		0.900 Biomarker disease GENOMICS_ENGLAND Ildr1b is essential for semicircular canal development, migration of the posterior lateral line primordium and hearing ability in zebrafish: implications for a role in the recessive hearing impairment DFNB42. 24990150 2014
Entrez Id: 286676
Gene Symbol: ILDR1
ILDR1 		0.900 GeneticVariation disease UNIPROT Loss-of-function mutations of ILDR1 cause autosomal-recessive hearing impairment DFNB42. 21255762 2011
Entrez Id: 286676
Gene Symbol: ILDR1
ILDR1 		0.900 Biomarker disease CTD_human
Entrez Id: 286676
Gene Symbol: ILDR1
ILDR1 		0.900 CausalMutation disease CLINVAR