Neonatal Alloimmune Thrombocytopenia Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Low platelet count associated with maternal platelet-specific alloantibodies. (Human Phenotype Ontology, HP_0004809)
External Link https://www.disgenet.org/browser/0/1/0/C3853779
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Genes

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

Symbol Name
ABO ABO blood group (transferase A, alpha 1-3-N-acetylgalactosaminyltransferase; transferase B, alpha 1-3-galactosyltransferase)
ADAR adenosine deaminase, RNA-specific
CACNB3 calcium channel, voltage-dependent, beta 3 subunit
CD109 CD109 molecule
CD36 CD36 molecule (thrombospondin receptor)
GP1BA glycoprotein Ib (platelet), alpha polypeptide
GP1BB glycoprotein Ib (platelet), beta polypeptide
GP9 glycoprotein IX (platelet)
HLA-DRB3 major histocompatibility complex, class II, DR beta 3
HLA-DRB4 major histocompatibility complex, class II, DR beta 4
HPSE heparanase
IFIH1 interferon induced with helicase C domain 1
ITGA2 integrin, alpha 2 (CD49B, alpha 2 subunit of VLA-2 receptor)
ITGA2B integrin, alpha 2b (platelet glycoprotein IIb of IIb/IIIa complex, antigen CD41)
ITGB3 integrin, beta 3 (platelet glycoprotein IIIa, antigen CD61)
MYH9 myosin, heavy chain 9, non-muscle
PLA2G1B phospholipase A2, group IB (pancreas)
PLA2G2A phospholipase A2, group IIA (platelets, synovial fluid)
PLA2G6 phospholipase A2, group VI (cytosolic, calcium-independent)
POU2F3 POU class 2 homeobox 3
PRB2 proline-rich protein BstNI subfamily 2
RICTOR RPTOR independent companion of MTOR, complex 2
RNASEH2A ribonuclease H2, subunit A
RNASEH2B ribonuclease H2, subunit B
RNASEH2C ribonuclease H2, subunit C
SAMD9 sterile alpha motif domain containing 9
SAMHD1 SAM domain and HD domain 1
SLC10A2 solute carrier family 10 (sodium/bile acid cotransporter), member 2
TREX1 three prime repair exonuclease 1