Fig. 2From: Investigation of SLA4A3 as a candidate gene for human retinal diseaseLocation of potentially pathogenic variants identified in RP patients on the AE3 protein. The number of amino acids that constitute each protein domain are indicated. SNPs_2 and _3 are located in the domains shared by the full-length (b) and cardiac (c) isoforms. SNP_1 is located in the N-terminal cytoplasmic domain unique to the full-length isoform (grey). SNP = single nucleotide polymorphismBack to article page