rs4984

This is a regulatory region variant variant in the ADD2 gene.

Research that mentions this SNP (1)

α- and β-Adducin polymorphisms affect podocyte proteins and proteinuria in rodents and decline of renal function in human IgA nephropathy
AssociationN=328Mara Ferrandi et al.(2010)· Journal of Molecular Medicine

This study demonstrates that α- and β-adducin polymorphisms affect podocyte protein expression and proteinuria in rodent models and are associated with the rate of renal function decline in human IgA nephropathy patients. The ADD2 1797T variant (rs4984) showed significant association with GFR decline (β=-4.66, p=0.0043), with significant interaction with ADD1 460Trp (rs4961, p=0.0174). Targeted deletion of β-adducin in mice reduced proteinuria and increased podocyte protein expression, while introduction of the polymorphic MHS β-adducin locus in normotensive rats caused early reduction in podocyte proteins, glomerular lesions, and proteinuria.

Traits studied:Blood pressureGlomerular diseaseIgA nephropathyProteinuriaRenal function decline

About ADD2

Adducins are heteromeric proteins composed of different subunits referred to as adducin alpha, beta and gamma. The three subunits are encoded by distinct genes and belong to a family of membrane skeletal proteins involved in the assembly of spectrin-actin network in erythrocytes and at sites of cell-cell contact in epithelial tissues. While adducins alpha and gamma are ubiquitously expressed, the expression of adducin beta is restricted to brain and hematopoietic tissues. Adducin, originally purified from human erythrocytes, was found to be a heterodimer of adducins alpha and beta. Polymorphisms resulting in amino acid substitutions in these two subunits have been associated with the regulation of blood pressure in an animal model of hypertension. Heterodimers consisting of alpha and gamma subunits have also been described. Structurally, each subunit is comprised of two distinct domains. The amino-terminal region is protease resistant and globular in shape, while the carboxy-terminal region is protease sensitive. The latter contains multiple phosphorylation sites for protein kinase C, the binding site for calmodulin, and is required for association with spectrin and actin. Alternatively spliced transcript variants have been described. [provided by RefSeq, Jun 2010]

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Gene information from NCBI Gene. Variant classifications from ClinVar.

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