De Novo Myelodysplastic Syndromes Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0280451
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Genes

25 genes associated with the disease De Novo Myelodysplastic Syndromes in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
BCL2L10 BCL2-like 10 (apoptosis facilitator)
CDKN2A cyclin-dependent kinase inhibitor 2A
CDKN2B cyclin-dependent kinase inhibitor 2B (p15, inhibits CDK4)
DCTN6 dynactin 6
DNAI1 dynein, axonemal, intermediate chain 1
FANCB Fanconi anemia, complementation group B
HPGDS hematopoietic prostaglandin D synthase
IDH2 isocitrate dehydrogenase 2 (NADP+), mitochondrial
IFI27 interferon, alpha-inducible protein 27
JAK2 Janus kinase 2
KMT2A lysine (K)-specific methyltransferase 2A
MVD mevalonate (diphospho) decarboxylase
NBN nibrin
NLRP2 NLR family, pyrin domain containing 2
PSMD9 proteasome (prosome, macropain) 26S subunit, non-ATPase, 9
RPS14 ribosomal protein S14
RUNX1 runt-related transcription factor 1
SEPT9 septin 9
SRSF2 serine/arginine-rich splicing factor 2
SSSCA1 Sjogren syndrome/scleroderma autoantigen 1
TICAM2 toll-like receptor adaptor molecule 2
TMED7 transmembrane emp24 protein transport domain containing 7
TMED7-TICAM2 TMED7-TICAM2 readthrough
TP53 tumor protein p53
U2AF1 U2 small nuclear RNA auxiliary factor 1