Congenital Thrombocytopenia Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Thrombocytopenia with congenital onset. (Human Phenotype Ontology, HP_0001905)
External Link https://www.disgenet.org/browser/0/1/0/C0272278
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Genes

18 genes associated with the disease Congenital Thrombocytopenia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ANKRD26 ankyrin repeat domain 26
CCR7 chemokine (C-C motif) receptor 7
ETV6 ets variant 6
GATA1 GATA binding protein 1 (globin transcription factor 1)
GNE glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase
HOXA11 homeobox A11
ITGA2B integrin, alpha 2b (platelet glycoprotein IIb of IIb/IIIa complex, antigen CD41)
ITGB3 integrin, beta 3 (platelet glycoprotein IIIa, antigen CD61)
KIF15 kinesin family member 15
MASTL microtubule associated serine/threonine kinase-like
MECOM MDS1 and EVI1 complex locus
MPL MPL proto-oncogene, thrombopoietin receptor
MYH9 myosin, heavy chain 9, non-muscle
NBEAL2 neurobeachin-like 2
PTPN11 protein tyrosine phosphatase, non-receptor type 11
SON SON DNA binding protein
THPO thrombopoietin
WAS Wiskott-Aldrich syndrome