Automated description from the Alliance of Genome Resources (Release 7.4.0)
Enables RS domain binding activity and mRNA binding activity. Involved in interleukin-17-mediated signaling pathway; protein localization to organelle; and regulation of gene expression. Acts upstream of or within RNA splicing; cardiac muscle contraction; and in utero embryonic development. Located in nuclear speck. Is expressed in several structures, including central nervous system; foregut; jaw; sensory organ; and thymus. Human ortholog(s) of this gene implicated in neurodevelopmental disorder with dysmorphic facies and behavioral abnormalities. Orthologous to human SRSF1 (serine and arginine rich splicing factor 1).
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