Varaico: Literature-Extracted Genetic Variants

Gene:CSF2RB
Variant:p.P603T
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CSF2RB

NM_000395.3:p.P603T

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

Hereditary pulmonary alveolar proteinosis caused by recessive CSF2RB mutations.

Suzuki T et al.

The European Respiratory Journal, 2011

Genome-wide analysis to predict protein sequence variations that change phosphorylation sites or their corresponding kinases.

Ryu GM et al.

Nucleic Acids Research, 2009

19139070 (PubMed )
Supplement: gkn1008_nar-01723-s-2008-File006.xls › TypeI_
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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."