MED21 mediator complex subunit 21
Gene ID: 9412, updated on 10-Oct-2024Gene type: protein coding
Also known as: SRB7; SURB7; hSrb7
- See all available tests in GTR for this gene
- Go to complete Gene record for MED21
- Go to Variation Viewer for MED21 variants
Summary
This gene encodes a member of the mediator complex subunit 21 family. The encoded protein interacts with the human RNA polymerase II holoenzyme and is involved in transcriptional regulation of RNA polymerase II transcribed genes. A pseudogene of this gene is located on chromosome 8. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2012]
Genomic context
- Location:
- 12p11.23
- Sequence:
- Chromosome: 12; NC_000012.12 (27022558..27038951)
- Total number of exons:
- 8
Variation
| Resource | Links for this gene |
|---|---|
| ClinVar | Variants reported to ClinVar |
| dbVar | Studies and variants |
| SNP | Variation Viewer for MED21 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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