Varaico: Literature-Extracted Genetic Variants

Gene:CSF2RA
Variant:p.A17G
Back to variants list

CSF2RA

NM_172245.4:p.A17G

Associated Papers

Neutrophil GM-CSF signaling in inflammatory bowel disease patients is influenced by non-coding genetic variants.

Venkateswaran S et al.

Scientific Reports, 2019

Genetic and Transcriptomic Variation Linked to Neutrophil Granulocyte-Macrophage Colony-Stimulating Factor Signaling in Pediatric Crohn's Disease.

Denson LA et al.

Inflammatory Bowel Diseases, 2019

Somatic mutations in clonally expanded cytotoxic T lymphocytes in patients with newly diagnosed rheumatoid arthritis.

Savola P et al.

Nature Communications, 2017

28635960 (PubMed )
Supplement: ncomms15869-s2.xlsx › list_of_variants

Characterization of CSF2RA mutation related juvenile pulmonary alveolar proteinosis.

Hildebrandt J et al.

Orphanet Journal of Rare Diseases, 2014

25425184 (PubMed )
Supplement: 13023_2014_171_MOESM1_ESM.docx

Hereditary pulmonary alveolar proteinosis. Could it be triggered by Mycoplasma pneumoniae pneumonia?

Santiago-Burruchaga M et al.

Respiratory Medicine, 2013

Converging evidence for a pseudoautosomal cytokine receptor gene locus in schizophrenia.

Lencz T et al.

Molecular Psychiatry, 2007

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."