基因名：
MAGOHB
产品别名：
MGN2； mago； magoh； MAGOHB； mago homolog B, exon junction complex subunit； mago homolog B, exon junction complex subunit； protein mago nashi homolog 2； mago homolog B, exon junction complex core component； mago-nashi homolog B； MAGOH蛋白；
背景信息：
MAGOHB (Mago Homolog B, Exon Junction Complex Subunit) is a Protein Coding gene. Diseases associated with MAGOHB include Metaphyseal Chondrodysplasia, Schmid Type and Chromosome 22Q11.2 Deletion Syndrome, Distal. Among its related pathways are Cleavage of Growing Transcript in the Termination Region and Transport of Mature Transcript to Cytoplasm. An important paralog of this gene is MAGOH.
