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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