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Lack of association between Connexin 31 (GJB3) alterations and sensorineural deafness in Austria.

Authors: Frei, Klemens  Ramsebner, Reinhard  Hamader, Gertrude  Lucas, Trevor  Schoefer, Christian  Baumgartner, Wolf-Dieter  Wachtler, Franz J  Kirschhofer, Karin 
Citation: Frei K, etal., Hear Res. 2004 Aug;194(1-2):81-6.
Pubmed: (View Article at PubMed) PMID:15276679
DOI: Full-text: DOI:10.1016/j.heares.2004.03.007

Mutations in the gap junction protein beta 3 (GJB3) gene encoding Connexin 31 (Cx31) are known to cause autosomal inherited sensorineural deafness, erythrokeratodermia and neuropathy. The role of Cx31 mutations has not been described in familial cases of non-syndromic hearing impairment (NSHI) in central European populations. To identify mutations in the Austrian population, highly selected familial (n=24) and sporadic (n=21) cases of isolated NSHI were screened by analysis of the complete coding sequence of Cx31, after exclusion of a common Cx26 causing deafness. Three different variations occurring in a total of 37% of all cases were identified. A C94T (R32W) missense mutation was seen in 4.4% of cases and two silent alterations C357T and C798T were detected in 8.9% and 24.4% of cases exclusively in a heterozygous pattern. No correlation between Cx31 alterations and deafness was found. To investigate the role of heterozygous Cx31 variations for a possibly combination allelic disease inheritance with Cx26 mutations as shown for Connexin 30 and Connexin 26, patients with Cx26 variations were tested. Our data suggest that Cx31 alterations are common but have no or a low genetic relevance in the Austrian hearing impaired population with or without Cx26 alterations.


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RGD Object Information
RGD ID: 12050154
Created: 2017-01-23
Species: All species
Last Modified: 2017-01-23
Status: ACTIVE


RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.