×
Entrez Id:
2070
Gene Symbol:
EYA4
EYA4
0.730
GeneticVariation
disease
CLINVAR
Exome sequencing reveals novel variants and unique allelic spectrum for hearing impairment in Filipino cochlear implantees.
30828794
2019
×
Entrez Id:
2070
Gene Symbol:
EYA4
EYA4
0.730
Biomarker
disease
BEFREE
Only four genetic midfrequency deafness genes, namely, DFNA10 (EYA4 ), DFNA8/12 (TECTA), DFNA13 (COL11A2), DFNA44 (CCDC50), have been reported to date.
27142990
2016
×
Entrez Id:
2070
Gene Symbol:
EYA4
EYA4
0.730
GeneticVariation
disease
BEFREE
A mutation in EYA4 was found in a Dutch family, causing DFNA10 .
26331839
2016
×
Entrez Id:
2070
Gene Symbol:
EYA4
EYA4
0.730
GeneticVariation
disease
CLINVAR
Evaluation of the contribution of the EYA4 and GRHL2 genes in Korean patients with autosomal dominant non-syndromic hearing loss.
25781927
2015
×
Entrez Id:
2070
Gene Symbol:
EYA4
EYA4
0.730
GeneticVariation
disease
UNIPROT
Exome Sequencing Identifies a Mutation in EYA4 as a Novel Cause of Autosomal Dominant Non-Syndromic Hearing Loss.
25961296
2015
×
Entrez Id:
2070
Gene Symbol:
EYA4
EYA4
0.730
GeneticVariation
disease
UNIPROT
A novel mutation of EYA4 in a large Chinese family with autosomal dominant middle-frequency sensorineural hearing loss by targeted exome sequencing.
25809937
2015
×
Entrez Id:
2070
Gene Symbol:
EYA4
EYA4
0.730
GeneticVariation
disease
UNIPROT
Targeted massive parallel sequencing: the effective detection of novel causative mutations associated with hearing loss in small families.
22938506
2012
×
Entrez Id:
2070
Gene Symbol:
EYA4
EYA4
0.730
GeneticVariation
disease
CLINVAR
Nonsyndromic hearing loss DFNA10 and a novel mutation of EYA4: evidence for correlation of normal cardiac phenotype with truncating mutations of the Eya domain.
17567890
2007
×
Entrez Id:
2070
Gene Symbol:
EYA4
EYA4
0.730
Biomarker
disease
GENOMICS_ENGLAND
Mutation in the transcriptional coactivator EYA4 causes dilated cardiomyopathy and sensorineural hearing loss.
15735644
2005
×
Entrez Id:
2070
Gene Symbol:
EYA4
EYA4
0.730
GeneticVariation
disease
CLINVAR
Mutation in the transcriptional coactivator EYA4 causes dilated cardiomyopathy and sensorineural hearing loss.
15735644
2005
×
Entrez Id:
2070
Gene Symbol:
EYA4
EYA4
0.730
GeneticVariation
disease
CLINVAR
Mutations in the transcriptional activator EYA4 cause late-onset deafness at the DFNA10 locus.
11159937
2001
×
Entrez Id:
2070
Gene Symbol:
EYA4
EYA4
0.730
GeneticVariation
disease
BEFREE
We present a detailed analysis of the DFNA10 phenotype based on data from 25 hearing-impaired persons coming from a large American pedigree segregating for deafness at the DFNA10 locus (chromosome 6q22.3-23.2).
11558763
2001
×
Entrez Id:
2070
Gene Symbol:
EYA4
EYA4
0.730
GeneticVariation
disease
UNIPROT
Mutations in the transcriptional activator EYA4 cause late-onset deafness at the DFNA10 locus.
11159937
2001
×
Entrez Id:
2070
Gene Symbol:
EYA4
EYA4
0.730
Biomarker
disease
GENOMICS_ENGLAND
EYA4, a novel vertebrate gene related to Drosophila eyes absent.
9887327
1999
×
Entrez Id:
2070
Gene Symbol:
EYA4
EYA4
0.730
CausalMutation
disease
CLINVAR
×
Entrez Id:
2070
Gene Symbol:
EYA4
EYA4
0.730
Biomarker
disease
CTD_human
×
Entrez Id:
100507308
Gene Symbol:
TARID
TARID
0.100
GeneticVariation
disease
CLINVAR
Evaluation of the contribution of the EYA4 and GRHL2 genes in Korean patients with autosomal dominant non-syndromic hearing loss.
25781927
2015
×
Entrez Id:
100507308
Gene Symbol:
TARID
TARID
0.100
GeneticVariation
disease
CLINVAR
Nonsyndromic hearing loss DFNA10 and a novel mutation of EYA4: evidence for correlation of normal cardiac phenotype with truncating mutations of the Eya domain.
17567890
2007
×
Entrez Id:
100507308
Gene Symbol:
TARID
TARID
0.100
GeneticVariation
disease
CLINVAR
Mutation in the transcriptional coactivator EYA4 causes dilated cardiomyopathy and sensorineural hearing loss.
15735644
2005
×
Entrez Id:
100507308
Gene Symbol:
TARID
TARID
0.100
GeneticVariation
disease
CLINVAR
Mutations in the transcriptional activator EYA4 cause late-onset deafness at the DFNA10 locus.
11159937
2001
×
Entrez Id:
7007
Gene Symbol:
TECTA
TECTA
0.010
Biomarker
disease
BEFREE
Only four genetic midfrequency deafness genes, namely, DFNA10 (EYA4 ), DFNA8 /12 (TECTA), DFNA13 (COL11A2), DFNA44 (CCDC50), have been reported to date.
27142990
2016