Varaico: Literature-Extracted Genetic Variants

Gene:FCN1
Variant:p.A218T
Back to variants list

FCN1

NM_002003.5:p.A218T

Associated Papers

Rare variants in complement system genes associate with endothelial damage after pediatric allogeneic hematopoietic stem cell transplantation.

Leimi L et al.

Frontiers in Immunology, 2023

37771589 (PubMed )
Supplement: DataSheet_2.pdf

Targeted Genotyping of MIS-C Patients Reveals a Potential Alternative Pathway Mediated Complement Dysregulation during COVID-19 Infection.

Gavriilaki E et al.

Current Issues in Molecular Biology, 2022

35877417 (PubMed )
Supplement: cimb-44-00193-s001.zip › cimb-1755355-supplementary.xlsx › AP_and_LP_variant_comparisons

Associations of Ficolins With Hematological Malignancies in Patients Receiving High-Dose Chemotherapy and Autologous Hematopoietic Stem Cell Transplantations.

Świerzko AS et al.

Frontiers in Immunology, 2019

Components of the lectin pathway of complement activation in paediatric patients of intensive care units.

Świerzko AS et al.

Immunobiology, 2016

Non-synonymous polymorphisms in the FCN1 gene determine ligand-binding ability and serum levels of M-ficolin.

Ammitzbøll CG et al.

Plos One, 2012

Select a paper to view details
UCSC Genome Browser·Imprint·Privacy·Terms·Feedback·Email Updates·

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."