Varaico: Literature-Extracted Genetic Variants

Gene:XIAP
Variant:p.K297T
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XIAP

NM_001167.4:p.K297T

Associated Papers

Analysis of Genes Associated With Monogenic Primary Immunodeficiency Identifies Rare Variants in XIAP in Patients With Crohn's Disease.

Amininejad L et al.

Gastroenterology, 2018

Nucleotide-binding oligomerization domain (NOD) signaling defects and cell death susceptibility cannot be uncoupled in X-linked inhibitor of apoptosis (XIAP)-driven inflammatory disease.

Chirieleison SM et al.

The Journal of Biological Chemistry, 2017

A de novo whole gene deletion of XIAP detected by exome sequencing analysis in very early onset inflammatory bowel disease: a case report.

Kelsen JR et al.

Bmc Gastroenterology, 2015

XIAP deficiency syndrome in humans.

Latour S et al.

Seminars in Cell & Developmental Biology, 2015

XIAP variants in male Crohn's disease.

Zeissig Y et al.

Gut, 2015

Inhibitors of apoptosis (IAPs) regulate intestinal immunity and inflammatory bowel disease (IBD) inflammation.

Pedersen J et al.

Trends in Molecular Medicine, 2014

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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."