abnormality of the lacrimal punctum Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of the lacrimal punctum, an opening on the eyelid close to the medial canthus that drains tears from the conjunctival sac into the lacrimal duct in the same eyelid. (Human Phenotype Ontology, HP_0011479)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0011479
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Genes

5 genes associated with the abnormality of the lacrimal punctum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
FGF10 fibroblast growth factor 10
FGFR2 fibroblast growth factor receptor 2
FGFR3 fibroblast growth factor receptor 3
TP63 tumor protein p63
UBR1 ubiquitin protein ligase E3 component n-recognin 1