Gene: P3H2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 55214
Gene Symbol: P3H2
P3H2 		0.310 Biomarker disease BEFREE In this study, differences in prolyl 3-hydroxylation were screened in eye tissues from P3h2-null (P3h2(n/n)) and wild-type mice to seek tissue-specific effects due the lack of P3H2 activity on post-translational collagen chemistry that could explain myopia. 25645914 2015
Entrez Id: 55214
Gene Symbol: P3H2
P3H2 		0.310 GermlineCausalMutation disease ORPHANET High myopia caused by a mutation in LEPREL1, encoding prolyl 3-hydroxylase 2. 21885030 2011