CRYM Chromosome 16
Crystallin mu
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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
RS1184938651
Conflicting classifications of pathogenicity
Health Risk
RS141936944
Conflicting classifications of pathogenicity
CRYM-related disorder, Autosomal dominant nonsyndromic hearing loss 40, CRYM-related disorder
Health Risk
RS143848148
Conflicting classifications of pathogenicity
Health Risk
RS145787995
Conflicting classifications of pathogenicity
CRYM-related disorder, CRYM-related disorder
Health Risk
RS147233841
Conflicting classifications of pathogenicity
Health Risk
RS149797560
Conflicting classifications of pathogenicity
Health Risk
RS201490017
Conflicting classifications of pathogenicity
Health Risk
RS371633413
Conflicting classifications of pathogenicity
CRYM-related disorder, CRYM-related disorder
Health Risk
RS386789728
Conflicting classifications of pathogenicity
Health Risk
RS727505275
Conflicting classifications of pathogenicity
Autosomal dominant nonsyndromic hearing loss 40, Autosomal dominant nonsyndromic hearing loss 40
Health Risk
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 |