Anti-Human /Mouse RCC1L Polyclonal Antibody

This gene encodes a protein containing regulator of chromosome condensation 1-like repeats. The encoded protein may function as a guanine nucleotide exchange factor. This gene is located in a region of chromosome 7 that is deleted in Williams-Beuren syndrome, a multisystem developmental disorder. Alternative splicing results in multiple transcript variants. RCC1L (RCC1 Like) is a Protein Coding gene. Diseases associated with RCC1L include Williams-Beuren Syndrome. An important paralog of this gene is RPGR.