hypoplasia of the pons Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Underdevelopment of the pons. (Human Phenotype Ontology, HP_0012110)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0012110
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11 genes associated with the hypoplasia of the pons phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ASNS asparagine synthetase (glutamine-hydrolyzing)
B3GALNT2 beta-1,3-N-acetylgalactosaminyltransferase 2
DOCK7 dedicator of cytokinesis 7
FKRP fukutin related protein
GMPPB GDP-mannose pyrophosphorylase B
LARGE like-glycosyltransferase
PMM2 phosphomannomutase 2
POMGNT1 protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-)
TSEN54 TSEN54 tRNA splicing endonuclease subunit
VRK1 vaccinia related kinase 1
WNT1 wingless-type MMTV integration site family, member 1