alacrima Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Absence of tear secretion. (Human Phenotype Ontology, HP_0000522)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000522
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Genes

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

Symbol Name
AAAS achalasia, adrenocortical insufficiency, alacrimia
DST dystonin
FGF10 fibroblast growth factor 10
FGFR2 fibroblast growth factor receptor 2
FGFR3 fibroblast growth factor receptor 3
GMPPA GDP-mannose pyrophosphorylase A
IKBKAP inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase complex-associated protein
PAX1 paired box 1
SETBP1 SET binding protein 1
SOX10 SRY (sex determining region Y)-box 10