Create issue ticket

2 Possible Causes for Mutation in the SLC39A5 Gene

  • Autosomal Dominant Myopia Type 24

    Gene Human Gene Mutation Database (HGMD) SLC39A5 SNPedia medical, phenotypic, and genealogical associations of SNPs for SLC39A5 No data available for Polymorphic Variants[genecards.org] Note The disease is caused by mutations affecting the gene represented in this entry.[genecards.org] Additional Disease Information for SLC39A5 No data available for Genatlas for SLC39A5 Gene The mammalian Zip5 protein is a zinc transporter that localizes to the basolateral[genecards.org]

  • Myopia

    […] in the CCDC111 gene (615421) on 4q35; MYP23 (615431), caused by mutation in the LRPAP1 gene (104225) on 4p16; MYP24 (615946), caused by mutation in the SLC39A5 gene (608730[ncbi.nlm.nih.gov] ) on 12q13; MYP25 (617238), caused by mutation in the P4HA2 gene (600608) on 5q31; and MYP26 (301010), caused by mutation in the ARR3 gene (301770) on Xq13.[ncbi.nlm.nih.gov] 14q22-q24; MYP19 (613969) on 5p15.1-p13.3; MYP20 (614166) on 13q12.12; MYP21 (614167), caused by mutation in the ZNF644 gene (614159) on 1p22; MYP22 (615420), caused by mutation[ncbi.nlm.nih.gov]

Further symptoms