CAPN10 Chromosome 2
Calpain 10
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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
RS1182803771
Pathogenic
Health Risk
RS1559425580
Pathogenic
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS2536286549
Pathogenic
CAPN10-related disorder, CAPN10-related disorder
Health Risk
RS2975760
risk factor
Type 2 diabetes mellitus 1, susceptibility to, Type 2 diabetes mellitus 1
Health Risk
RS3792267
risk factor
Type 2 diabetes mellitus 1, susceptibility to, Type 2 diabetes mellitus 1
Health Risk
RS3842570
risk factor
Type 2 diabetes mellitus 1, susceptibility to, Type 2 diabetes mellitus 1
Health Risk
RS5030952
risk factor
Type 2 diabetes mellitus 1, susceptibility to, Type 2 diabetes mellitus 1
Health Risk
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 |