Varaico: Literature-Extracted Genetic Variants

Gene:FCGR3A
Variant:p.L66H
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FCGR3A

NM_000569.8:p.L66H

Associated Papers

Complete CD16A Deficiency and Defective NK Cell Function in a Man Living with HIV.

Zhang W et al.

Journal of Clinical Immunology, 2025

Fc gamma receptor polymorphisms in antibody therapy: implications for bioassay development to enhance product quality.

Twomey JD et al.

Antibody Therapeutics, 2025

NK Cytotoxicity Mediated by NK-92 Cell Lines Expressing Combinations of Two Allelic Variants for FCGR3.

Freitas Monteiro M et al.

Antibodies (basel, Switzerland), 2024

ACE Phenotyping in Human Blood and Tissues: Revelation of ACE Outliers and Sex Differences in ACE Sialylation.

Enyedi EE et al.

Biomedicines, 2024

38790902 (PubMed )
Supplement: biomedicines-12-00940-s001.zip › biomedicines-2930173-supplementary.pdf

Association of NK cell subsets and cytotoxicity with FCGR3A gene polymorphism in functional NK cell deficiency.

Karaselek MA et al.

Revista Da Associacao Medica Brasileira (1992), 2024

Undetectable NK Cells due to the FCGR3A Variant, L66H, Which May Not Be Directly Disease-Causing.

Izadi N et al.

Journal of Clinical Immunology, 2021

Allotype-specific processing of the CD16a N45-glycan from primary human natural killer cells and monocytes.

Patel KR et al.

Glycobiology, 2020

Workflow for the Implementation of Precision Genomics in Healthcare.

Mehandziska S et al.

Frontiers in Genetics, 2020

32695137 (PubMed )
Supplement: Data_Sheet_2.XLSX › Rare_diseases

Natural killer cell biology illuminated by primary immunodeficiency syndromes in humans.

Voss M et al.

Clinical Immunology (orlando, Fla.), 2017

iFish: predicting the pathogenicity of human nonsynonymous variants using gene-specific/family-specific attributes and classifiers.

Wang M et al.

Scientific Reports, 2016

27527004 (PubMed )
Supplement: srep31321-s4.xls › SwissvarFilteredMix

Genetic Causes of Human NK Cell Deficiency and Their Effect on NK Cell Subsets.

Mace EM et al.

Frontiers in Immunology, 2016

Natural killer cell deficiency.

Orange JS

The Journal of Allergy and Clinical Immunology, 2013

Human immunodeficiency-causing mutation defines CD16 in spontaneous NK cell cytotoxicity.

Grier JT et al.

The Journal of Clinical Investigation, 2012

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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."