Mediator complex subunit 9 (Med9) is a protein that in humans is encoded by the MED9 gene. [5]
MED9 | |||||||||||||||||||||||||||||||||||||||||||||||||||
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Aliases | MED9, MED25, mediator complex subunit 9 | ||||||||||||||||||||||||||||||||||||||||||||||||||
External IDs | OMIM: 609878; MGI: 2183151; HomoloGene: 32385; GeneCards: MED9; OMA:MED9 - orthologs | ||||||||||||||||||||||||||||||||||||||||||||||||||
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Function
editThe multiprotein Mediator complex is a coactivator required for activation of RNA polymerase II transcription by DNA bound transcription factors. The protein encoded by this gene is thought to be a subunit of the Mediator complex. This gene is located within the Smith–Magenis syndrome region on chromosome 17. [provided by RefSeq, Jul 2008].
See also
editReferences
edit- ^ a b c GRCh38: Ensembl release 89: ENSG00000141026 – Ensembl, May 2017
- ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000061650 – Ensembl, May 2017
- ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ "Entrez Gene: Mediator complex subunit 9". Retrieved 2018-02-06.
Further reading
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This article incorporates text from the United States National Library of Medicine, which is in the public domain.