miosis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Abnormal (non-physiological) constriction of the pupil. (Human Phenotype Ontology, HP_0000616)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000616
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Genes

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

Symbol Name
DDC dopa decarboxylase (aromatic L-amino acid decarboxylase)
NME1 NME/NM23 nucleoside diphosphate kinase 1
ORAI1 ORAI calcium release-activated calcium modulator 1
PHYH phytanoyl-CoA 2-hydroxylase
SIX6 SIX homeobox 6
STIM1 stromal interaction molecule 1