CRYM Chromosome 16

Crystallin mu
10 variants 10 Health Risk

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What This Gene Does
Crystallins are separated into two classes: taxon-specific and ubiquitous. The former class is also called phylogenetically-restricted crystallins. The latter class constitutes the major proteins of vertebrate eye lens and maintains the transparency and refractive index of the lens. This gene encodes a taxon-specific crystallin protein that binds NADPH and has sequence similarity to bacterial ornithine cyclodeaminases. The encoded protein does not perform a structural role in lens tissue, and instead it binds thyroid hormone for possible regulatory or developmental roles. Mutations in this gene have been associated with autosomal dominant non-syndromic deafness. [provided by RefSeq, Sep 2014]
Associated Conditions (2)
CRYM-related disorder
Autosomal dominant nonsyndromic hearing loss 40
Key Variants
All Variants (10)
RSID Category Clinical Significance Conditions
RS1184938651 Health Risk Conflicting classifications of pathogenicity
RS141936944 Health Risk Conflicting classifications of pathogenicity CRYM-related disorder, Autosomal dominant nonsyndromic hearing loss 40, CRYM-related disorder
RS143848148 Health Risk Conflicting classifications of pathogenicity
RS145787995 Health Risk Conflicting classifications of pathogenicity CRYM-related disorder, CRYM-related disorder
RS147233841 Health Risk Conflicting classifications of pathogenicity
RS149797560 Health Risk Conflicting classifications of pathogenicity
RS201490017 Health Risk Conflicting classifications of pathogenicity
RS371633413 Health Risk Conflicting classifications of pathogenicity CRYM-related disorder, CRYM-related disorder
RS386789728 Health Risk Conflicting classifications of pathogenicity
RS727505275 Health Risk Conflicting classifications of pathogenicity Autosomal dominant nonsyndromic hearing loss 40, Autosomal dominant nonsyndromic hearing loss 40
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