rectal prolapse Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002035
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Genes

8 genes associated with the rectal prolapse phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
BMPR1A bone morphogenetic protein receptor, type IA
CCBE1 collagen and calcium binding EGF domains 1
CFTR cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7)
LTBP4 latent transforming growth factor beta binding protein 4
NAA10 N(alpha)-acetyltransferase 10, NatA catalytic subunit
RPS6KA3 ribosomal protein S6 kinase, 90kDa, polypeptide 3
SMAD4 SMAD family member 4
STK11 serine/threonine kinase 11