OLFM2, olfactomedin 2, 93145

N. diseases: 14; N. variants: 7
Disease: Disorder of eye ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0015397
Disease: Disorder of eye
Disorder of eye 		0.020 GeneticVariation group BEFREE Identification and functional characterisation of genetic variants in OLFM2 in children with developmental eye disorders. 27844144 2017
CUI: C0015397
Disease: Disorder of eye
Disorder of eye 		0.020 Biomarker group BEFREE Noelin 1 and Noelin 2 could be tested as candidate genes for eye diseases based on their expressions in the eye and shared olfactomedin domains with Myocilin in the C-termini of the respective proteins. 15123989 2004