TEX28, testis expressed 28, 1527

N. diseases: 6; N. variants: 0
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0155015
Disease: Color Blindness, Red
Color Blindness, Red 		0.010 GeneticVariation disease BEFREE Genomic DNA from five pedigrees (with high myopia and either protanopia or deuteranopia) that mapped to Xq28 were screened for TEX28 copy number variations (CNVs) and sequence variants. 19098318 2009
CUI: C0155016
Disease: Color Blindness, Red-Green
Color Blindness, Red-Green 		0.010 GeneticVariation disease BEFREE Genomic DNA from five pedigrees (with high myopia and either protanopia or deuteranopia) that mapped to Xq28 were screened for TEX28 copy number variations (CNVs) and sequence variants. 19098318 2009
CUI: C0271183
Disease: Severe myopia
Severe myopia 		0.010 GeneticVariation disease BEFREE Genomic DNA from five pedigrees (with high myopia and either protanopia or deuteranopia) that mapped to Xq28 were screened for TEX28 copy number variations (CNVs) and sequence variants. 19098318 2009
CUI: C1839612
Disease: MYOPIA 1, X-LINKED
MYOPIA 1, X-LINKED 		0.010 GeneticVariation disease BEFREE TEX28 gene CNVs appear to be associated with the MYP1 X-linked myopia phenotypes. 19098318 2009
CUI: C4551635
Disease: Deuteranopia
Deuteranopia 		0.010 GeneticVariation disease BEFREE Genomic DNA from five pedigrees (with high myopia and either protanopia or deuteranopia) that mapped to Xq28 were screened for TEX28 copy number variations (CNVs) and sequence variants. 19098318 2009
CUI: C4551767
Disease: Protanopia
Protanopia 		0.010 GeneticVariation disease BEFREE Genomic DNA from five pedigrees (with high myopia and either protanopia or deuteranopia) that mapped to Xq28 were screened for TEX28 copy number variations (CNVs) and sequence variants. 19098318 2009