rs1009388
This is a regulatory region variant variant in the POMC gene.
▶Research that mentions this SNP (1)
▶Association between variants in the genes for leptin, leptin receptor, and proopiomelanocortin with chronic heart failure in the Czech populationAssociationN=779Julie Anna Bienertová-Vašků et al.(2009)· Heart and Vessels
Case-control study in 372 Czech CHF patients and 407 controls examining variants in leptin, leptin receptor, and proopiomelanocortin genes. While LEP and POMC variants showed no overall case-control association, the LEPR Gln223Arg polymorphism demonstrated significant independent associations with CHF progression: approximately 2-fold increased risk for NYHA class IV (OR=2.10, p<0.0000001) and prediction of reduced LVEF (OR=4.05, p=0.002), with stronger effects in dilated cardiomyopathy (OR=11.87 for LVEF, p=0.004).
About POMC
This gene encodes a preproprotein that undergoes extensive, tissue-specific, post-translational processing via cleavage by subtilisin-like enzymes known as prohormone convertases. There are eight potential cleavage sites within the preproprotein and, depending on tissue type and the available convertases, processing may yield as many as ten biologically active peptides involved in diverse cellular functions. The encoded protein is synthesized mainly in corticotroph cells of the anterior pituitary where four cleavage sites are used; adrenocorticotrophin, essential for normal steroidogenesis and the maintenance of normal adrenal weight, and lipotropin beta are the major end products. In other tissues, including the hypothalamus, placenta, and epithelium, all cleavage sites may be used, giving rise to peptides with roles in pain and energy homeostasis, melanocyte stimulation, and immune modulation. These include several distinct melanotropins, lipotropins, and endorphins that are contained within the adrenocorticotrophin and beta-lipotropin peptides. The antimicrobial melanotropin alpha peptide exhibits antibacterial and antifungal activity. Mutations in this gene have been associated with early onset obesity, adrenal insufficiency, and red hair pigmentation. Alternatively spliced transcript variants encoding the same protein have been described. [provided by RefSeq, Jan 2016]
View all POMC variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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