Placental Dysfunction Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C1395512
Similar Terms
Downloads & Tools

Genes

28 genes associated with the disease Placental Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ACO1 aconitase 1, soluble
ADIPOQ adiponectin, C1Q and collagen domain containing
AFP alpha-fetoprotein
ALOX15 arachidonate 15-lipoxygenase
BCL2 B-cell CLL/lymphoma 2
CDKN1C cyclin-dependent kinase inhibitor 1C (p57, Kip2)
ERVW-1 endogenous retrovirus group W, member 1
FGR FGR proto-oncogene, Src family tyrosine kinase
FLT1 fms-related tyrosine kinase 1
FPR2 formyl peptide receptor 2
HMOX1 heme oxygenase 1
HSD11B2 hydroxysteroid (11-beta) dehydrogenase 2
IGF1 insulin-like growth factor 1 (somatomedin C)
IGF2 insulin-like growth factor 2
IL1A interleukin 1, alpha
IL1B interleukin 1, beta
KNG1 kininogen 1
MAPK14 mitogen-activated protein kinase 14
PAPPA pregnancy-associated plasma protein A, pappalysin 1
PGF placental growth factor
PHLDA2 pleckstrin homology-like domain, family A, member 2
PPARG peroxisome proliferator-activated receptor gamma
PTH1R parathyroid hormone 1 receptor
RAMP2 receptor (G protein-coupled) activity modifying protein 2
RASSF1 Ras association (RalGDS/AF-6) domain family member 1
TGIF1 TGFB-induced factor homeobox 1
THBD thrombomodulin
TNF tumor necrosis factor