breech presentation Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A position of the fetus at delivery in which the fetus enters the birth canal with the buttocks or feet first. (Human Phenotype Ontology, HP_0001623)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001623
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Genes

10 genes associated with the breech presentation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
COL1A1 collagen, type I, alpha 1
COL1A2 collagen, type I, alpha 2
CRTAP cartilage associated protein
DHCR7 7-dehydrocholesterol reductase
KLHL41 kelch-like family member 41
MKS1 Meckel syndrome, type 1
MYH3 myosin, heavy chain 3, skeletal muscle, embryonic
ORC1 origin recognition complex, subunit 1
PEX1 peroxisomal biogenesis factor 1
SLC26A2 solute carrier family 26 (anion exchanger), member 2