DFNB31
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Template:Short description Template:Infobox gene
Whirlin is a protein that in humans is encoded by the DFNB31 gene.[1][2][3]
In rat brain, WHRN interacts with a calmodulin-dependent serine kinase, CASK, and may be involved in the formation of scaffolding protein complexes that facilitate synaptic transmission in the central nervous system (CNS).[4] Mutations in this gene, also known as WHRN, cause autosomal recessive deafness.[3]
References
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Further reading
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