Source: UNIPROT

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 283375
Gene Symbol: SLC39A5
SLC39A5
CUI: C4014762
Disease: MYOPIA 24, AUTOSOMAL DOMINANT
MYOPIA 24, AUTOSOMAL DOMINANT 		0.600 GeneticVariation UNIPROT SLC39A5 mutations interfering with the BMP/TGF-β pathway in non-syndromic high myopia. 24891338

2014
Entrez Id: 283375
Gene Symbol: SLC39A5
SLC39A5
CUI: C4014762
Disease: MYOPIA 24, AUTOSOMAL DOMINANT
MYOPIA 24, AUTOSOMAL DOMINANT 		0.600 GeneticVariation UNIPROT Detection of mutations in LRPAP1, CTSH, LEPREL1, ZNF644, SLC39A5, and SCO2 in 298 families with early-onset high myopia by exome sequencing. 25525168

2014