abnormal delivery Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of the birth process. (Human Phenotype Ontology, HP_0001787)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001787
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28 genes associated with the abnormal delivery phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ADAMTS2 ADAM metallopeptidase with thrombospondin type 1 motif, 2
COL1A1 collagen, type I, alpha 1
COL1A2 collagen, type I, alpha 2
COL5A1 collagen, type V, alpha 1
COL5A2 collagen, type V, alpha 2
CRTAP cartilage associated protein
DHCR7 7-dehydrocholesterol reductase
FGA fibrinogen alpha chain
FGB fibrinogen beta chain
FGG fibrinogen gamma chain
HOXA13 homeobox A13
HTR1A 5-hydroxytryptamine (serotonin) receptor 1A, G protein-coupled
JAK2 Janus kinase 2
KLHL41 kelch-like family member 41
LMNA lamin A/C
MGP matrix Gla protein
MKS1 Meckel syndrome, type 1
MPL MPL proto-oncogene, thrombopoietin receptor
MYH3 myosin, heavy chain 3, skeletal muscle, embryonic
ORC1 origin recognition complex, subunit 1
PEX1 peroxisomal biogenesis factor 1
PLOD1 procollagen-lysine, 2-oxoglutarate 5-dioxygenase 1
SERPINH1 serpin peptidase inhibitor, clade H (heat shock protein 47), member 1, (collagen binding protein 1)
SLC26A2 solute carrier family 26 (anion exchanger), member 2
SYCP3 synaptonemal complex protein 3
THPO thrombopoietin
XIST X inactive specific transcript (non-protein coding)
ZMPSTE24 zinc metallopeptidase STE24