prominent umbilicus Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Abnormally prominent umbilicus (belly button). (Human Phenotype Ontology, HP_0001544)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001544
Similar Terms
Downloads & Tools

Genes

4 genes associated with the prominent umbilicus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AGPAT2 1-acylglycerol-3-phosphate O-acyltransferase 2
BSCL2 Berardinelli-Seip congenital lipodystrophy 2 (seipin)
FGD1 FYVE, RhoGEF and PH domain containing 1
PTRF polymerase I and transcript release factor