PRR12 Rabbit Polyclonal Antibody, 50ul General Lab Use problems with gluconeogenesis and lipogenesis

problems with gluconeogenesis and lipogenesis

A splice-site mutation in this gene has been associated with a novel progressive myoclonic epilepsy disease with similar symptoms to MERRF syndrome

This gene encodes an enzyme that transfers methyl groups to cytosine nucleotides of genomic DNA

A protein encoded by this human locus has been found to localize to pre-mRNA splicing complexes in the nucleus and is necessary for pre-mRNA splicing

The mature peptide may also form heterodimers with other TGFB family members

PRR12 Rabbit Polyclonal Antibody, 50ul General Lab Use problems with gluconeogenesis and lipogenesisThis gene encodes a proline rich protein that contains two A T hook DNA binding domains. A chromosomal translocation and gene fusion between this gene and zinc finger MIZ type containing 1 (Gene ID: 57178) may underlie intellectual disability and neuropsychiatric problems in a human patient. Enriched expression of this gene in embryonic mouse brain suggests that this gene may play a role in nervous system development.