Varaico: Literature-Extracted Genetic Variants

Gene:RGS2
Variant:p.Q2L
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RGS2

NM_002923.4:p.Q2L

Associated Papers

N-Terminal Targeting of Regulator of G Protein Signaling Protein 2 for F-Box Only Protein 44-Mediated Proteasomal Degradation.

McNabb HJ et al.

Molecular Pharmacology, 2020

A Global Map of G Protein Signaling Regulation by RGS Proteins.

Masuho I et al.

Cell, 2020

33007266 (PubMed )
Supplement: mmc5.xlsx › RGS2

Loss-of-Function Mutations in Human Regulator of G Protein Signaling RGS2 Differentially Regulate Pharmacological Reactivity of Resistance Vasculature.

Phan HTN et al.

Molecular Pharmacology, 2019

Genetic Analysis of Rare Human Variants of Regulators of G Protein Signaling Proteins and Their Role in Human Physiology and Disease.

Squires KE et al.

Pharmacological Reviews, 2018

Proteolytic degradation of regulator of G protein signaling 2 facilitates temporal regulation of Gq/11 signaling and vascular contraction.

Kanai SM et al.

The Journal of Biological Chemistry, 2017

Human Missense Mutations in Regulator of G Protein Signaling 2 Affect the Protein Function Through Multiple Mechanisms.

Phan HTN et al.

Molecular Pharmacology, 2017

FBXO44-Mediated Degradation of RGS2 Protein Uniquely Depends on a Cullin 4B/DDB1 Complex.

Sjögren B et al.

Plos One, 2015

The RGS2 gene product from a candidate hypertension allele shows decreased plasma membrane association and inhibition of Gq.

Gu S et al.

Molecular Pharmacology, 2008

N-terminal residues control proteasomal degradation of RGS2, RGS4, and RGS5 in human embryonic kidney 293 cells.

Bodenstein J et al.

Molecular Pharmacology, 2007

Genetic variations of regulator of G-protein signaling 2 in hypertensive patients and in the general population.

Yang J et al.

Journal of Hypertension, 2005

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Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."