Automated description from the Alliance of Genome Resources (Release 7.4.0)
Predicted to enable mRNA binding activity. Acts upstream of or within nuclear-transcribed mRNA catabolic process, nonsense-mediated decay and positive regulation of mRNA cis splicing, via spliceosome. Located in neuronal cell body and nucleus. Is expressed in several structures, including central nervous system. Human ortholog(s) of this gene implicated in syndromic X-linked intellectual disability 14. Orthologous to human UPF3B (UPF3B regulator of nonsense mediated mRNA decay).
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