|
| Entrez Id: |
7007 |
| Gene Symbol: |
TECTA |
TECTA
|
Nonsyndromic Deafness
|
0.330 |
Biomarker |
CLINGEN |
A novel TECTA mutation causes ARNSHL.
|
28012541 |
2017 |
|
| Entrez Id: |
7007 |
| Gene Symbol: |
TECTA |
TECTA
|
Nonsyndromic Deafness
|
0.330 |
Biomarker |
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
|
Nonsyndromic Deafness
|
0.330 |
Biomarker |
CLINGEN |
Otolith tethering in the zebrafish otic vesicle requires Otogelin and α-Tectorin.
|
25758224 |
2015 |
|
| Entrez Id: |
7007 |
| Gene Symbol: |
TECTA |
TECTA
|
Nonsyndromic Deafness
|
0.330 |
Biomarker |
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
|
Nonsyndromic Deafness
|
0.330 |
Biomarker |
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
|
Nonsyndromic Deafness
|
0.330 |
Biomarker |
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
|
Nonsyndromic Deafness
|
0.330 |
Biomarker |
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
|
Nonsyndromic Deafness
|
0.330 |
Biomarker |
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
|
Nonsyndromic Deafness
|
0.330 |
Biomarker |
CLINGEN |
A novel TECTA mutation confirms the recognizable phenotype among autosomal recessive hearing impairment families.
|
18022253 |
2008 |
|
| Entrez Id: |
7007 |
| Gene Symbol: |
TECTA |
TECTA
|
Nonsyndromic Deafness
|
0.330 |
Biomarker |
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
|
Nonsyndromic Deafness
|
0.330 |
Biomarker |
CLINGEN |
A deafness mutation isolates a second role for the tectorial membrane in hearing.
|
15995703 |
2005 |
|
| Entrez Id: |
7007 |
| Gene Symbol: |
TECTA |
TECTA
|
Nonsyndromic Deafness
|
0.330 |
Biomarker |
CLINGEN |
A genotype-phenotype correlation with gender-effect for hearing impairment caused by TECTA mutations.
|
15319541 |
2004 |
|
| Entrez Id: |
7007 |
| Gene Symbol: |
TECTA |
TECTA
|
Nonsyndromic Deafness
|
0.330 |
Biomarker |
CLINGEN |
Distinctive audiometric profile associated with DFNB21 alleles of TECTA.
|
12746400 |
2003 |
|
| Entrez Id: |
7007 |
| Gene Symbol: |
TECTA |
TECTA
|
Nonsyndromic Deafness
|
0.330 |
Biomarker |
CLINGEN |
Quantification of TECTA and DFNA5 expression in the developing mouse cochlea.
|
11711860 |
2001 |
|
| Entrez Id: |
7007 |
| Gene Symbol: |
TECTA |
TECTA
|
Nonsyndromic Deafness
|
0.330 |
Biomarker |
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
|
Nonsyndromic Deafness
|
0.330 |
Biomarker |
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
|
Nonsyndromic Deafness
|
0.330 |
Biomarker |
CLINGEN |
Mutations in the human alpha-tectorin gene cause autosomal dominant non-syndromic hearing impairment.
|
9590290 |
1998 |