ZMAT3 Polyclonal Antibody, 100ul Custom RNA Oligos Defects in this gene are

Defects in this gene are the cause of congenital stationary night blindness type 1 (CSNB1)| also called X-linked congenital stationary night blindness (XLCSNB)

are composed of an alpha

Together with RAB11A

which is important in a wide range of cellular activities: neuronal

ZMAT3 Polyclonal Antibody, 100ul Custom RNA Oligos Defects in this gene areThis gene encodes a protein containing three zinc finger domains and a nuclear localization signal. The mRNA and the protein of this gene are upregulated by wildtype p53 and overexpression of this gene inhibits tumor cell growth, suggesting that this gene may have a role in the p53 dependent growth regulatory pathway. Alternative splicing of this gene results in two transcript variants encoding two isoforms differing in only one amino acid.