Varaico: Literature-Extracted Genetic Variants

Gene:TNFSF13
Variant:p.G67R
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TNFSF13

NM_003808.4:p.G67R

Associated Papers

Population-specific putative causal variants shape quantitative traits.

Koyama S et al.

Nature Genetics, 2024

39363016 (PubMed )
Supplement: 41588_2024_1913_MOESM3_ESM.xlsx › ST8_Missense_PPI___0.1

Association of genetic variation in COL11A1 with adolescent idiopathic scoliosis.

Yu H et al.

Elife, 2024

38277211 (PubMed )
Supplement: elife-89762-supp1.xlsx › Variants

Analysis across Taiwan Biobank, Biobank Japan, and UK Biobank identifies hundreds of novel loci for 36 quantitative traits.

Chen CY et al.

Cell Genomics, 2023

Association of genetic variation in COL11A1 with adolescent idiopathic scoliosis.

Yu H et al.

Biorxiv : the Preprint Server for Biology, 2023

37292598 (PubMed )
Supplement: media-1.xlsx › Variants

Protein and functional isoform levels and genetic variants of the BAFF and APRIL pathway components in systemic lupus erythematosus.

Ortiz-Aljaro P et al.

Scientific Reports, 2022

Variants of genes encoding TNF receptors and ligands and proteins regulating TNF activation in familial multiple sclerosis.

Torre-Fuentes L et al.

Cns Neuroscience & Therapeutics, 2020

32951330 (PubMed )
Supplement: CNS-26-1178-s002.xlsx › Hoja1

Association of Common Variants of TNFSF13 and TNFRSF13B Genes with CLL Risk and Clinical Picture, as Well as Expression of Their Products-APRIL and TACI Molecules.

Jasek M et al.

Cancers, 2020

33036273 (PubMed )
Supplement: cancers-12-02873-s001.pdf

XAF1 as a modifier of p53 function and cancer susceptibility.

Pinto EM et al.

Science Advances, 2020

32637605 (PubMed )
Supplement: aba3231_Table_S1.xlsx › Table_S1

Identification of TNFSF13, SPATC1L, SLC22A25 and SALL4 as novel susceptibility loci for atrial fibrillation by an exome‑wide association study.

Yamada Y et al.

Molecular Medicine Reports, 2017

Neutropenia in Patients with Common Variable Immunodeficiency: a Rare Event Associated with Severe Outcome.

Guffroy A et al.

Journal of Clinical Immunology, 2017

Identification of sequence variants influencing immunoglobulin levels.

Jonsson S et al.

Nature Genetics, 2017

APRIL gene polymorphism and serum sAPRIL levels in children with systemic lupus erythematosus.

Namazi S et al.

Clinical Rheumatology, 2017

Characterization of Disease-Associated Mutations in Human Transmembrane Proteins.

Molnár J et al.

Plos One, 2016

26986070 (PubMed )
Supplement: pone.0151760.s001.xlsx › polymorphism

Effects of APRIL (TNFSF13) polymorphisms and splicing isoforms on the secretion of soluble APRIL.

Furuya T et al.

Modern Rheumatology, 2012

Association of common variants in TNFRSF13B, TNFSF13, and ANXA3 with serum levels of non-albumin protein and immunoglobulin isotypes in Japanese.

Osman W et al.

Plos One, 2012

Genome-wide scan identifies variant in TNFSF13 associated with serum IgM in a healthy Chinese male population.

Yang M et al.

Plos One, 2012

Cumulative association of eight susceptibility genes with systemic lupus erythematosus in a Japanese female population.

Koga M et al.

Journal of Human Genetics, 2011

[IgA subclass and IgA deficiency].

Kaneko H et al.

Nihon Rinsho Men'eki Gakkai Kaishi = Japanese Journal of Clinical Immunology, 2009

Screening of functional and positional candidate genes in families with common variable immunodeficiency.

Salzer U et al.

Bmc Immunology, 2008

APRIL polymorphism and systemic lupus erythematosus (SLE) susceptibility.

Lee YH et al.

Rheumatology (oxford, England), 2007

Role of APRIL (TNFSF13) polymorphisms in the susceptibility to systemic lupus erythematosus in Japanese.

Kawasaki A et al.

Rheumatology (oxford, England), 2007

A novel polymorphism of the human APRIL gene is associated with systemic lupus erythematosus.

Koyama T et al.

Rheumatology (oxford, England), 2003

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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."