Automated description from the Alliance of Genome Resources (Release 3.1.1)
Predicted to be involved in SCF-dependent proteasomal ubiquitin-dependent protein catabolic process; positive regulation of neuron projection development; and protein K48-linked ubiquitination. Localizes to cytoplasm and nucleus. Is expressed in central nervous system and retina. Human ortholog(s) of this gene implicated in distal hereditary motor neuronopathy type 2D. Orthologous to human FBXO38 (F-box protein 38).