stillbirth Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Death of the fetus in utero after at least 20 weeks of gestation. (Human Phenotype Ontology, HP_0003826)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0003826
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Genes

24 genes associated with the stillbirth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ALPL alkaline phosphatase, liver/bone/kidney
COL11A1 collagen, type XI, alpha 1
COL2A1 collagen, type II, alpha 1
DOK7 docking protein 7
ESCO2 establishment of sister chromatid cohesion N-acetyltransferase 2
FLNA filamin A, alpha
FLNB filamin B, beta
GDF5 growth differentiation factor 5
HBZ hemoglobin, zeta
HYLS1 hydrolethalus syndrome 1
LBR lamin B receptor
LMNA lamin A/C
NEK8 NIMA-related kinase 8
NSDHL NAD(P) dependent steroid dehydrogenase-like
OSTM1 osteopetrosis associated transmembrane protein 1
PHGDH phosphoglycerate dehydrogenase
PTEN phosphatase and tensin homolog
PTH1R parathyroid hormone 1 receptor
RAPSN receptor-associated protein of the synapse
RNU4ATAC RNA, U4atac small nuclear (U12-dependent splicing)
SLC26A2 solute carrier family 26 (anion exchanger), member 2
SLC35D1 solute carrier family 35 (UDP-GlcA/UDP-GalNAc transporter), member D1
TRIP11 thyroid hormone receptor interactor 11
ZMPSTE24 zinc metallopeptidase STE24