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.