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PMID: 10369879 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Mutations in the KCNQ4 gene are responsible for autosomal dominant deafness in four DFNA2 families.

Human molecular genetics ·Vol. 8 ·No. 7 ·1999-07-00 ·Pages 1321-8

Coucke PJ, Van Hauwe P, Kelley PM, Kunst H, Schatteman I, Van Velzen D, Meyers J, Ensink RJ, Verstreken M, Declau F, Marres H, Kastury K, Bhasin S, McGuirt WT, Smith RJ, Cremers CW, Van de Heyning P, Willems PJ, Smith SD, Van Camp G

Abstract

We have previously found linkage to chromosome 1p34 in five large families with autosomal dominant non-syndromic hearing impairment (DFNA2). In all five families, the connexin31 gene ( GJB3 ), located at 1p34 and responsible for non-syndromic autosomal dominant hearing loss in two small Chinese families, has been excluded as the responsible gene. Recently, a fourth member of the KCNQ branch of the K+channel family, KCNQ4, has been cloned. KCNQ4 was mapped to chromosome 1p34 and a single mutation was found in three patients from a small French family with non-syndromic autosomal dominant hearing loss. In this study, we have analysed the KCNQ4 gene for mutations in our five DFNA2 families. Missense mutations altering conserved amino acids were found in three families and an inactivating deletion was present in a fourth family. No KCNQ4 mutation could be found in a single DFNA2 family of Indonesian origin. These results indicate that at least two and possibly three genes responsible for hearing impairment are located close together on chromosome 1p34 and suggest that KCNQ4 mutations may be a relatively frequent cause of autosomal dominant hearing loss.

MeSH Terms
Amino Acid Sequence Chromosome Mapping Chromosomes, Human, Pair 1 DNA Mutational Analysis Deafness/genetics Expressed Sequence Tags Female Genetic Linkage Genetic Markers Humans KCNQ Potassium Channels Male Molecular Sequence Data Mutation Potassium Channels/genetics Potassium Channels, Voltage-Gated Sequence Alignment Sequence Homology, Amino Acid
Chemicals
Genetic Markers KCNQ Potassium Channels KCNQ4 protein, human Potassium Channels Potassium Channels, Voltage-Gated
Authors & Affiliations
20 authors, click to expand affiliations / ORCID
Coucke P J
Department of Medical Genetics, University of Antwerp-UIA, Universiteitsplein 1, 2610 Antwerp, Belgium,
Van Hauwe P
Kelley P M
Kunst H
Schatteman I
Van Velzen D
Meyers J
Ensink R J
Verstreken M
Declau F
Marres H
Kastury K
Bhasin S
McGuirt W T
Smith R J
Cremers C W
Van de Heyning P
Willems P J
Smith S D
Van Camp G
Article Info
Journal
Human molecular genetics
Abbr.
Hum Mol Genet
ISSN
0964-6906
Published
1999-07-00
Pages
1321-8
Language
English
Region
England
NLM ID
9208958
Subset
IM
Grants
NCRR NIH HHS · P20RR11145-01 · United States
NIDCD NIH HHS · R01 DC02942-03 · United States
NIDCD NIH HHS · R01DCO2842 · United States
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