High Risk Myelodysplastic Syndrome Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C4528176
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Genes

18 genes associated with the disease High Risk Myelodysplastic Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ABCB1 ATP-binding cassette, sub-family B (MDR/TAP), member 1
ATM ATM serine/threonine kinase
CBL Cbl proto-oncogene, E3 ubiquitin protein ligase
CD34 CD34 molecule
CSF3R colony stimulating factor 3 receptor (granulocyte)
DCK deoxycytidine kinase
FLT3 fms-related tyrosine kinase 3
IL1RAP interleukin 1 receptor accessory protein
IL2 interleukin 2
MLLT11 myeloid/lymphoid or mixed-lineage leukemia (trithorax homolog, Drosophila); translocated to, 11
NFKB1 nuclear factor of kappa light polypeptide gene enhancer in B-cells 1
NPM1 nucleophosmin (nucleolar phosphoprotein B23, numatrin)
NR0B2 nuclear receptor subfamily 0, group B, member 2
PLCB1 phospholipase C, beta 1 (phosphoinositide-specific)
PTPN6 protein tyrosine phosphatase, non-receptor type 6
RPS14 ribosomal protein S14
RUNX1 runt-related transcription factor 1
TBC1D9 TBC1 domain family, member 9 (with GRAM domain)