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Reported incidences for these genes in an international population of patients with albinism are 7% for SLC45A2 , 1% for TYRP1 , and less than 0.5% for SLC24A5 .[86] SLC45A2 is found in 24% of oculocutaneous albinism cases in Japan, making it the most common type of albinism among Japanese individuals with identifiable variants.[87] A study of 22 individuals of Italian ancestry without pathogenic variants in TYR , OCA2 , or TYRP1 found 5 individuals with biallelic variants in SLC45A2 , 4 of whom met clinical criteria for a diagnosis of oculocutaneous albinism.[88] Collectively, more than 600 unique ocular albinismrelated genetic variants have been identified.[89] OCA4 is thought to be similar to other types of albinism, but the increased risk of SCC of the skin in people with these variants has not been quantified

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Tarbashevich et al., has displayed light-controlled protein expression in Zebrafish embryo in vivo model, where they were able to induce the expression of fluorescent proteins for cell labelling, toxins for targeted cell ablation, and morphogens like Bmp2b and -catenin to influence embryonic development [51]

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