Predicted to enable calcium ion binding activity. Predicted to be involved in several processes, including positive regulation of response to oxidative stress; skeletal muscle fiber development; and skeletal muscle satellite cell maintenance involved in skeletal muscle regeneration. Predicted to act upstream of or within several processes, including cellular response to caffeine; positive regulation of skeletal muscle cell proliferation; and response to muscle activity involved in regulation of muscle adaptation. Predicted to be active in endoplasmic reticulum membrane. Human ortholog(s) of this gene implicated in rigid spine muscular dystrophy 1. Orthologous to human SELENON (selenoprotein N); INTERACTS WITH gentamycin; paracetamol; thioacetamide.
[INS protein co-treated with Dexamethasone co-treated with 1-Methyl-3-isobutylxanthine co-treated with Indomethacin co-treated with bisphenol A] results in decreased expression of SEPN1 mRNA
[INS protein co-treated with Dexamethasone co-treated with 1-Methyl-3-isobutylxanthine co-treated with Indomethacin co-treated with bisphenol A] results in decreased expression of SEPN1 mRNA
[[Gasoline co-treated with 1-Butanol] results in increased abundance of [Particulate Matter co-treated with Polycyclic Aromatic Hydrocarbons]] which results in increased expression of SEPN1 mRNA
[INS protein co-treated with Dexamethasone co-treated with 1-Methyl-3-isobutylxanthine co-treated with Indomethacin co-treated with bisphenol A] results in decreased expression of SEPN1 mRNA
[INS protein co-treated with Dexamethasone co-treated with 1-Methyl-3-isobutylxanthine co-treated with Indomethacin co-treated with bisphenol A] results in decreased expression of SEPN1 mRNA
[[Gasoline co-treated with isobutyl alcohol] results in increased abundance of [Particulate Matter co-treated with Polycyclic Aromatic Hydrocarbons]] which results in increased expression of SEPN1 mRNA