
CAPN10 Gene - GeneCards | CAN10 Protein | CAN10 Antibody
2025年3月30日 · CAPN10 (Calpain 10) is a Protein Coding gene. Diseases associated with CAPN10 include Type 1 Diabetes Mellitus 2 and Polycystic Ovary Syndrome. Among its related pathways are DREAM Repression and Dynorphin Expression and …
CAPN10 - Wikipedia
It is an atypical calpain in that it lacks the calmodulin-like calcium-binding domain and instead has a divergent C-terminal domain. It therefore cannot heterodimerize with the small subunit. It is similar in organization to calpains 5 and 6.
Type 2 diabetes candidate gene CAPN10: first, but not last
CAPN10, which encodes the cysteine protease calpain 10, was the first type 2 diabetes mellitus (T2DM) susceptibility gene identified through a genome-wide scan followed by positional cloning. A haplotype combination comprising three intronic CAPN10 single-nucleotide polymorphisms (UCSNP-43, -19, and …
11132 - Gene ResultCAPN10 calpain 10 [ (human)] - National …
2025年2月10日 · CAPN10 alleles are associated with polycystic ovary syndrome; We show that the diabetes gene calpain-10 (CAPN10) plays a role in atherosclerosis, insulin sensitivity and insulin secretion in a population enriched for atherosclerosis and insulin resistance. polymorphism influences glucose metabolism in human fat cells
钙蛋白酶 10(CAPN10)基因 | MCE - MCE-生物活性分子大师
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.
CAPN10 - an overview | ScienceDirect Topics
CAPN10 is ubiquitously distributed, and its cellular localization is dynamic. When localized to the mitochondria, it mediates mitochondrial dysfunction by cleaving Complex I subunits and promotes mitochondrial permeability transition. CAPN10 is also involved in GLUT4 vesicle translocation during insulin-stimulated glucose uptake in adipocytes.
CAPN10 calpain 10 - NIH Genetic Testing Registry (GTR) - NCBI
2025年1月4日 · 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.
Calpain-10: from genome search to function - PubMed
Calpain-10 (CAPN10) is the first diabetes gene to be identified through a genome scan. Many investigators, but not all, have subsequently found associations between CAPN10 polymorphism and type 2 diabetes (T2D) as well as insulin action, insulin secretion, aspects of adipocyte biology and microvascu …
CAPN10基因详情-基因数据库-基因云馆 - Genelibs
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.
Entry - *605286 - CALPAIN 10; CAPN10 - OMIM
The CAPN10 gene encodes a ubiquitously expressed member of the calpain-like cysteine protease family. The 672 amino-acid protein shares 81.7% identity with the mouse ortholog. CAPN10 was expressed as major and minor transcripts of 2.7 and 4.0 kb, respectively, present at low levels in all adult and fetal tissues examined, with slightly higher ...