×
Entrez Id:
7007
Gene Symbol:
TECTA
TECTA
0.330
Biomarker
disease
CLINGEN
A novel TECTA mutation causes ARNSHL.
28012541
2017
×
Entrez Id:
7007
Gene Symbol:
TECTA
TECTA
0.330
Biomarker
disease
CLINGEN
Tectorins crosslink type II collagen fibrils and connect the tectorial membrane to the spiral limbus.
26806019
2016
×
Entrez Id:
7007
Gene Symbol:
TECTA
TECTA
0.330
Biomarker
disease
CLINGEN
Otolith tethering in the zebrafish otic vesicle requires Otogelin and α-Tectorin.
25758224
2015
×
Entrez Id:
7007
Gene Symbol:
TECTA
TECTA
0.330
Biomarker
disease
CLINGEN
Whole-exome sequencing reveals diverse modes of inheritance in sporadic mild to moderate sensorineural hearing loss in a pediatric population.
25719458
2015
×
Entrez Id:
7007
Gene Symbol:
TECTA
TECTA
0.330
GeneticVariation
disease
BEFREE
A novel mutation in the TECTA gene in a Chinese family with autosomal dominant nonsyndromic hearing loss .
24586623
2014
×
Entrez Id:
7007
Gene Symbol:
TECTA
TECTA
0.330
Biomarker
disease
CLINGEN
Three deaf mice: mouse models for TECTA-based human hereditary deafness reveal domain-specific structural phenotypes in the tectorial membrane.
24363064
2014
×
Entrez Id:
7007
Gene Symbol:
TECTA
TECTA
0.330
GeneticVariation
disease
BEFREE
A novel missense mutation c.6016 G > T (p.Asp2006Tyr ) of TECTA gene is a characteristic TECTA -related mutation which causes autosomal dominant nonsyndromic hearing loss .
25008054
2014
×
Entrez Id:
7007
Gene Symbol:
TECTA
TECTA
0.330
Biomarker
disease
CLINGEN
TECTA mutations in Japanese with mid-frequency hearing loss affected by zona pellucida domain protein secretion.
22718023
2012
×
Entrez Id:
7007
Gene Symbol:
TECTA
TECTA
0.330
Biomarker
disease
CLINGEN
DFNA8/12 caused by TECTA mutations is the most identified subtype of nonsyndromic autosomal dominant hearing loss.
21520338
2011
×
Entrez Id:
7007
Gene Symbol:
TECTA
TECTA
0.330
Biomarker
disease
CLINGEN
Deficient forward transduction and enhanced reverse transduction in the alpha tectorin C1509G human hearing loss mutation.
20142329
2010
×
Entrez Id:
7007
Gene Symbol:
TECTA
TECTA
0.330
Biomarker
disease
CLINGEN
A novel TECTA mutation confirms the recognizable phenotype among autosomal recessive hearing impairment families.
18022253
2008
×
Entrez Id:
7007
Gene Symbol:
TECTA
TECTA
0.330
Biomarker
disease
CLINGEN
Identification of three novel TECTA mutations in Iranian families with autosomal recessive nonsyndromic hearing impairment at the DFNB21 locus.
17431902
2007
×
Entrez Id:
7007
Gene Symbol:
TECTA
TECTA
0.330
Biomarker
disease
CLINGEN
A deafness mutation isolates a second role for the tectorial membrane in hearing.
15995703
2005
×
Entrez Id:
7007
Gene Symbol:
TECTA
TECTA
0.330
Biomarker
disease
CLINGEN
A genotype-phenotype correlation with gender-effect for hearing impairment caused by TECTA mutations.
15319541
2004
×
Entrez Id:
7007
Gene Symbol:
TECTA
TECTA
0.330
Biomarker
disease
CLINGEN
Distinctive audiometric profile associated with DFNB21 alleles of TECTA.
12746400
2003
×
Entrez Id:
7007
Gene Symbol:
TECTA
TECTA
0.330
Biomarker
disease
CLINGEN
Quantification of TECTA and DFNA5 expression in the developing mouse cochlea.
11711860
2001
×
Entrez Id:
7007
Gene Symbol:
TECTA
TECTA
0.330
Biomarker
disease
CLINGEN
A targeted deletion in alpha-tectorin reveals that the tectorial membrane is required for the gain and timing of cochlear feedback.
11087000
2000
×
Entrez Id:
7007
Gene Symbol:
TECTA
TECTA
0.330
Biomarker
disease
CLINGEN
An alpha-tectorin gene defect causes a newly identified autosomal recessive form of sensorineural pre-lingual non-syndromic deafness, DFNB21.
9949200
1999
×
Entrez Id:
7007
Gene Symbol:
TECTA
TECTA
0.330
GeneticVariation
disease
BEFREE
Mapping of the alpha-tectorin gene (TECTA ) to mouse chromosome 9 and human chromosome 11: a candidate for human autosomal dominant nonsyndromic deafness .
9503015
1998
×
Entrez Id:
7007
Gene Symbol:
TECTA
TECTA
0.330
Biomarker
disease
CLINGEN
Mutations in the human alpha-tectorin gene cause autosomal dominant non-syndromic hearing impairment.
9590290
1998