Aliases for MAGOHB Gene
External Ids for MAGOHB Gene
Previous GeneCards Identifiers for MAGOHB Gene
GeneCards Summary for MAGOHB Gene
MAGOHB (Mago Homolog B, Exon Junction Complex Subunit) is a Protein Coding gene. Diseases associated with MAGOHB include Metaphyseal Chondrodysplasia, Schmid Type and Primary Autosomal Recessive Microcephaly. Among its related pathways are Gene Expression and Transport of Mature Transcript to Cytoplasm. An important paralog of this gene is MAGOH.
UniProtKB/Swiss-Prot Summary for MAGOHB Gene
Required for pre-mRNA splicing as component of the spliceosome (PubMed:28502770, PubMed:29301961, PubMed:30705154). Plays a redundant role with MAGOH in the exon junction complex and in the nonsense-mediated decay (NMD) pathway (PubMed:23917022).