Homo sapiens calpain-like protease CAPN10d mRNA, complete cds

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Molecular role of non-exonic variants in CALPAIN 10 gene in polycystic ovarian syndrome in Saudi women. [Front Endocrinol (Lausanne). 2...]
Molecular role of non-exonic variants in CALPAIN 10 gene in polycystic ovarian syndrome in Saudi women.
Alageel AA, Alshammary AF, Ali Khan I. Front Endocrinol (Lausanne). 2023; 14:1303747. Epub 2023 Dec 27.
Correlation between TCF7L2 and CAPN10 gene polymorphisms and gestational diabetes mellitus in different geographical regions: a meta-analysis. [BMC Pregnancy Childbirth. 2024]
Correlation between TCF7L2 and CAPN10 gene polymorphisms and gestational diabetes mellitus in different geographical regions: a meta-analysis.
He J, Zhang M, Ren J, Jiang X. BMC Pregnancy Childbirth. 2024 Jan 2; 24(1):15. Epub 2024 Jan 2.
Dysregulated miRNA-375, IL-17, TGF-β, and Microminerals Are Associated with Calpain-10 SNP 19 in Diabetic Patients: Correlation with Diabetic Nephropathy Stages. [Int J Mol Sci. 2023]
Dysregulated miRNA-375, IL-17, TGF-β, and Microminerals Are Associated with Calpain-10 SNP 19 in Diabetic Patients: Correlation with Diabetic Nephropathy Stages.
Ezzat GM, Azoz NMA, El Zohne RA, Abdellatif H, Saleem TH, Emam WA, Mohammed AR, Mohamed SA, Muhammed AA, Abd El-Rady NM, et al. Int J Mol Sci. 2023 Dec 13; 24(24). Epub 2023 Dec 13.

RefSeq alternative splicing
See 2 reference mRNA sequence splice variants for the CAPN10 gene.

Homo sapiens calpain-like protease CAPN10d mRNA, complete cds
Homo sapiens calpain-like protease CAPN10d mRNA, complete cds
gi|10503943|gb|AF089092.1|

Nucleotide
LOC127888520 [Homo sapiens]
LOC127888520 [Homo sapiens]
Gene ID:127888520

Gene
LOC127888514 [Homo sapiens]
LOC127888514 [Homo sapiens]
Gene ID:127888514

Gene
Enuresis
Enuresis
Involuntary discharge of URINE after expected age of completed development of urinary control. This can happen during the daytime (DIURNAL ENURESIS) while one is awake or duri...<br/>

MeSH
Neurodevelopmental Disorders
Neurodevelopmental Disorders
These are a group of conditions with onset in the developmental period. The disorders typically manifest early in development, often before the child enters grade school, and ...<br/>Year introduced: 2015 (1998)

MeSH

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Nucleotide