MEF-2C Polyclonal Antibody, 50ul Bottles Mutations in this gene cause

Mutations in this gene cause hereditary sensory and autonomic neuropathy with spastic paraplegia (HSNSP)

The V1 domain consists of three A and three B subunits

which are encoded by three separate genes

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Among its related pathways are mRNA Splicing - Major Pathway

MEF-2C Polyclonal Antibody, 50ul Bottles Mutations in this gene causeMEF2C encodes a member of the MADS box transcription enhancer factor 2 (MEF2) family of proteins, which play a role in myogenesis. The encoded protein, MEF2 polypeptide C, has both trans activating and DNA binding activities. This protein may play a role in maintaining the differentiated state of muscle cells. Mutations and deletions at this locus have been associated with severe mental retardation, stereotypic movements, epilepsy, and cerebral