CAPN10 Chromosome 2

Calpain 10
7 variants 7 Health Risk

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What This Gene Does
Calpains represent a ubiquitous, well-conserved family of calcium-dependent cysteine proteases. The calpain proteins are heterodimers consisting of an invariant small subunit and variable large subunits. The large catalytic subunit has four domains: domain I, the N-terminal regulatory domain that is processed upon calpain activation; domain II, the protease domain; domain III, a linker domain of unknown function; and domain IV, the calmodulin-like calcium-binding domain. This gene encodes a large subunit. It is an atypical calpain in that it lacks the calmodulin-like calcium-binding domain and instead has a divergent C-terminal domain. It is similar in organization to calpains 5 and 6. This gene is associated with type 2 or non-insulin-dependent diabetes mellitus (NIDDM), and is located within the NIDDM1 region. Multiple alternative transcript variants have been described for this gene. [provided by RefSeq, Sep 2010]
Gene Info
Gene Group
Calpains
Locus Type
gene with protein product
Location
2q37.3
Ensembl
ENSG00000142330
Associated Conditions (4)
Inborn genetic diseases
CAPN10-related disorder
Type 2 diabetes mellitus 1
susceptibility to
Key Variants
All Variants (7)
RSID Category Clinical Significance Conditions
RS1182803771 Health Risk Pathogenic
RS1559425580 Health Risk Pathogenic Inborn genetic diseases, Inborn genetic diseases
RS2536286549 Health Risk Pathogenic CAPN10-related disorder, CAPN10-related disorder
RS2975760 Health Risk risk factor Type 2 diabetes mellitus 1, susceptibility to, Type 2 diabetes mellitus 1
RS3792267 Health Risk risk factor Type 2 diabetes mellitus 1, susceptibility to, Type 2 diabetes mellitus 1
RS3842570 Health Risk risk factor Type 2 diabetes mellitus 1, susceptibility to, Type 2 diabetes mellitus 1
RS5030952 Health Risk risk factor Type 2 diabetes mellitus 1, susceptibility to, Type 2 diabetes mellitus 1
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