Varaico: Literature-Extracted Genetic Variants

Gene:RHAG
Variant:p.I61R
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RHAG

NM_000324.3:p.I61R

Associated Papers

Next generation sequencing (NGS) interest in deciphering erythrocyte molecular defects' association in red cell disorders: Clinical and erythrocyte phenotypes of patients with mutations inheritance in PIEZO1, Spectrin ß1, RhAG and SLC4A1.

Allegrini B et al.

Blood Cells, Molecules & Diseases, 2023

An erythrocyte-centric view on the MFSD2B sphingosine-1-phosphate transporter.

Ghaderi S et al.

Pharmacology & Therapeutics, 2023

Diagnosis and clinical management of red cell membrane disorders.

Kalfa TA

Hematology. American Society of Hematology. Education Program, 2021

Red Blood Cell Membrane Conductance in Hereditary Haemolytic Anaemias.

Petkova-Kirova P et al.

Frontiers in Physiology, 2019

Overhydrated stomatocytosis associated with a complex RHAG genotype including a novel de novo mutation.

Jamwal M et al.

Journal of Clinical Pathology, 2018

The Molecular Basis for Altered Cation Permeability in Hereditary Stomatocytic Human Red Blood Cells.

Flatt JF et al.

Frontiers in Physiology, 2018

Advances in understanding the pathogenesis of the red cell volume disorders.

Badens C et al.

British Journal of Haematology, 2016

Compound heterozygosity of two novel RHAG alleles leads to a considerable disruption of the Rh complex.

Polin H et al.

Transfusion, 2016

Disorders of erythrocyte volume homeostasis.

Glogowska E et al.

International Journal of Laboratory Hematology, 2015

SNPs altering ammonium transport activity of human Rhesus factors characterized by a yeast-based functional assay.

Deschuyteneer A et al.

Plos One, 2013

Human RhAG ammonia channel is impaired by the Phe65Ser mutation in overhydrated stomatocytic red cells.

Genetet S et al.

American Journal of Physiology. Cell Physiology, 2012

Loss-of-function and gain-of-function phenotypes of stomatocytosis mutant RhAG F65S.

Stewart AK et al.

American Journal of Physiology. Cell Physiology, 2011

Determinants of erythrocyte hydration.

Rinehart J et al.

Current Opinion in Hematology, 2010

The Rh protein family: gene evolution, membrane biology, and disease association.

Huang CH et al.

Cellular and Molecular Life Sciences : Cmls, 2010

A new blood group system, RHAG: three antigens resulting from amino acid substitutions in the Rh-associated glycoprotein.

Tilley L et al.

Vox Sanguinis, 2010

The monovalent cation leak in overhydrated stomatocytic red blood cells results from amino acid substitutions in the Rh-associated glycoprotein.

Bruce LJ et al.

Blood, 2009

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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."