POU2F1, POU class 2 homeobox 1, 5451

N. diseases: 115; N. variants: 7
Disease: Miosis disorder ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0026205
Disease: Miosis disorder
Miosis disorder 		0.010 Biomarker disease BEFREE Volunteers carrying loss-of-function OCT1 polymorphisms had significantly higher plasma concentrations of O-desmethyltramadol (P = 0.002, n = 41) and significantly prolonged miosis, a surrogate marker of opioidergic effects (P = 0.005, n = 24). 21562485 2011