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This gene is a paralog of SMN1 gene, which encodes the survival motor neuron protein, mutations in which are cause of autosomal recessive proximal spinal muscular atrophy. The protein encoded by this gene is a nuclear protein that has been identified as a constituent of the spliceosome complex. This gene is differentially expressed, with abundant levels in skeletal muscle, and may share similar cellular function as the SMN1 gene. Protein function: Necessary for spliceosome assembly. Overexpression causes apoptosis. [The UniProt Consortium]
Keywords:
Anti-SMNR, Anti-SMNDC1, Anti-SMN-related protein, Anti-30 kDa splicing factor SMNrp, Anti-Survival motor neuron domain-containing protein 1, Anti-Survival of motor neuron-related-splicing factor 30, SMNDC1 Polyclonal Antibody
This website uses cookies, which are necessary for the technical operation of the website and are always set. Other cookies, which increase the usability of this website, serve for direct advertising or simplify interaction with other websites and social networks, will only be used with your consent.
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