Predicted to enable polyubiquitin modification-dependent protein binding activity. Involved in DNA damage response. Located in nucleus. Expressed widely. Human ortholog(s) of this gene implicated in Ruijs-Aalfs syndrome. Is an ortholog of human SPRTN (SprT-like N-terminal domain).
Map position created from combination of previous interpolated map position (based on known location of sequence) and allele information. Therefore this is not a genetic map position based on recombination frequencies or genetic experiments. This was done on advice of the CGC.