Varaico: Literature-Extracted Genetic Variants

Gene:FOXN1
Variant:p.P465fs
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FOXN1

NM_001369369.1:p.P465fs

Associated Papers

Informed clinical decisions by outfoxing human FOXN1 variants.

Wysocki CA et al.

The Journal of Allergy and Clinical Immunology, 2025

Utilization of next-generation sequencing to define the role of heterozygous FOXN1 variants in immunodeficiency.

Pasternak Y et al.

The Journal of Allergy and Clinical Immunology. Global, 2024

Comprehensive phenotypic analysis of diverse FOXN1 variants.

Moses A et al.

The Journal of Allergy and Clinical Immunology, 2023

Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations.

Giardino G et al.

Journal of Clinical Immunology, 2021

Heterozygous FOXN1 Variants Cause Low TRECs and Severe T Cell Lymphopenia, Revealing a Crucial Role of FOXN1 in Supporting Early Thymopoiesis.

Bosticardo M et al.

American Journal of Human Genetics, 2019

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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."