Source: BEFREE

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4657
Gene Symbol: MYP1
MYP1
CUI: C0271183
Disease: Severe myopia
Severe myopia 		0.080 Biomarker BEFREE The unique LVAVA haplotype in OPN1LW was detected in the family with X-linked nonsyndromic high myopia mapped to MYP1. 26114493

2015
Entrez Id: 4657
Gene Symbol: MYP1
MYP1
CUI: C0271183
Disease: Severe myopia
Severe myopia 		0.080 GeneticVariation BEFREE Refinement of the X-linked nonsyndromic high-grade myopia locus MYP1 on Xq28 and exclusion of 13 known positional candidate genes by direct sequencing. 21357393

2011
Entrez Id: 4657
Gene Symbol: MYP1
MYP1
CUI: C0271183
Disease: Severe myopia
Severe myopia 		0.080 GeneticVariation BEFREE In addition, our results suggest that color visual defects and optic disc hypoplasia are not necessary signs of high myopia attributed to the MYP1 region. 21060050

2010
Entrez Id: 4657
Gene Symbol: MYP1
MYP1
CUI: C0271183
Disease: Severe myopia
Severe myopia 		0.080 GeneticVariation BEFREE Many genetic mutations linked to the development of HM have been described, including high grade myopia, and MYP1-16; different patterns of inheritance may reflect different types of HM. 19865068

2009
Entrez Id: 4657
Gene Symbol: MYP1
MYP1
CUI: C0271183
Disease: Severe myopia
Severe myopia 		0.080 GeneticVariation BEFREE Evaluation of the X-linked high-grade myopia locus (MYP1) with cone dysfunction and color vision deficiencies. 19098318

2009
Entrez Id: 4657
Gene Symbol: MYP1
MYP1
CUI: C0271183
Disease: Severe myopia
Severe myopia 		0.080 Biomarker BEFREE Confirmation of a genetic locus for X-linked recessive high myopia outside MYP1. 17351708

2007
Entrez Id: 4657
Gene Symbol: MYP1
MYP1
CUI: C0271183
Disease: Severe myopia
Severe myopia 		0.080 Biomarker BEFREE Novel locus for X linked recessive high myopia maps to Xq23-q25 but outside MYP1. 16648373

2006
Entrez Id: 4657
Gene Symbol: MYP1
MYP1
CUI: C0271183
Disease: Severe myopia
Severe myopia 		0.080 GeneticVariation BEFREE The disease maps to chromosome Xq28 and is the first designated high-grade myopia locus (MYP1). 15197065

2004