MAGOHB mago homolog B, exon junction complex subunit
Gene ID: 55110, updated on 17-Jun-2024Gene type: protein coding
Also known as: MGN2; mago; magoh
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- Go to complete Gene record for MAGOHB
- Go to Variation Viewer for MAGOHB variants
Summary
Enables RNA binding activity. Involved in mRNA splicing, via spliceosome and nuclear-transcribed mRNA catabolic process, nonsense-mediated decay. Located in nucleus. Part of U2-type catalytic step 1 spliceosome; U2-type precatalytic spliceosome; and exon-exon junction complex. [provided by Alliance of Genome Resources, Apr 2022]
Genomic context
- Location:
- 12p13.2
- Sequence:
- Chromosome: 12; NC_000012.12 (10599524..10613609, complement)
- Total number of exons:
- 8
Variation
| Resource | Links for this gene |
|---|---|
| ClinVar | Variants reported to ClinVar |
| dbVar | Studies and variants |
| SNP | Variation Viewer for MAGOHB variants |
| Genome viewer | Explore NCBI-annotated and select non-NCBI annotated genome assemblies |
- ClinVarRelated medical variations
- dbVarLink from Gene to dbVar
- OMIMLink to related OMIM entry
- PubMed (OMIM)Gene links to PubMed derived from omim_pubmed_cited links
- RefSeq RNAsLink to Nucleotide RefSeq RNAs
- Variation ViewerRelated Variants
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