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KCNQ4 : a gene for age‐related hearing impairment?
Author(s) -
Van Eyken E.,
Van Laer L.,
Fransen E.,
Topsakal V.,
Lemkens N.,
Laureys W.,
Nelissen N.,
Vandevelde A.,
Wienker T.,
Van De Heyning P.,
Van Camp G.
Publication year - 2006
Publication title -
human mutation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.981
H-Index - 162
eISSN - 1098-1004
pISSN - 1059-7794
DOI - 10.1002/humu.20375
Subject(s) - single nucleotide polymorphism , linkage disequilibrium , biology , genetics , snp , locus (genetics) , population , allele frequency , candidate gene , tag snp , genotype , gene , medicine , environmental health
Abstract Age‐related hearing impairment (ARHI) is the most common sensory impairment among the elderly. It is a complex disorder influenced by genetic as well as environmental factors. SNPs in a candidate susceptibility gene, KCNQ4 , were examined in two independent Caucasian populations. Two quantitative trait locus (QTL) values were investigated: Z high and Z low , a measure of high and respectively low frequency hearing loss. In the first population, the statistical analysis of 23 genotyped SNPs spread across KCNQ4 resulted in significant p‐values for two SNPs for Z high —SNP9 (NT_004511:g.11244177A>T) and SNP15 (NT_004511:g.11257005C>T; NP_004691:p.Ala259Ala), and one SNP for Z low —SNP12 (NT_004511:g.11249550A>T). The linkage disequilibrium (LD) structure of KCNQ4 was subsequently determined in a 34‐kb region surrounding the significant SNPs, resulting in three LD‐blocks. LD‐block 1 contains SNP9 and covers an area of 5 kb, LD‐block 2 measures 5 kb and surrounds SNP13 (NT_004511:g.11253513A>G) to SNP18 (NT_004511:g.11257509G>A; NP_004691:p.Thr293Thr), and LD‐block 3 spans 7 kb. Five tag‐SNPs of block 1 and 2, and 2 extra SNPs were subsequently genotyped in the second population. Again, several SNPs were positively associated with ARHI: one SNP (SNP18) for the high frequencies and three SNPs (SNP9, SNP12, and SNP18) for the low frequencies, although only a single SNP (SNP12) resulted in significant p‐values in both populations. Nevertheless, the associated SNPs of both populations were all located in the same 13‐kb region in the middle of the KCNQ4 gene. Hum Mutat 27(10), 1007–1016, 2006. © 2006 Wiley‐Liss, Inc.