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solute carrier family 26, member 5 (prestin)
This gene is a member of the SLC26A/SulP transporter family. It encodes a protein that is specifically expressed in outer hair cells (OHCs) of the cochlea and is essential in auditory processing. Intracellular anions are thought to act as extrinsic voltage sensors, which bind to this protein and trigger the conformational changes required for rapid length changes in OHCs. Mutations in this gene have been associated with non-syndromic hearing loss. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq]
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| Synovial membrane |
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| Penis |
86
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| Deltoid |
83
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| Cardia of stomach |
81
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| Stomach |
80
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| Methylnitronitrosogu… |
100
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| Lithium |
100
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| Zinc00028150 |
98
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| Gemfibrozil |
94
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| Indomethacin |
93
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| Methylglyoxal |
91
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Authors: Morag A Lewis, Elizabeth Quint, Anne M Glazier, Helmut Fuchs, Martin Hrabé De Angelis, Cordelia Langford, Stijn van Dongen, Cei Abreu-Goodger, Matias Piipari, Nick Redshaw,…
Nature genetics 2009 MayAuthors: Dominik Oliver, Thorsten Schächinger, Bernd Fakler
Novartis Foundation symposium 2006Thought leaders and organizations working on research involving SLC26A5.