For example, the p. Gly380Arg mutation in the FGFR3 protein is believed to be responsible for achondroplasia, [28]; the p. Gly185Arg change in the NRAMP2 protein results in microcytic aneamia in humans [29]; the p. Gly796Arg variation in the Band3 protein causes hereditary stomatocytosis [30]. Here, SLC11A2 is linked to achondroplasia.