MED9
Mediator complex subunit 9 (Med9) is a protein that in humans is encoded by the MED9 gene. [4]
| MED9 | |||||||||||||||||||||||||
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| Aliases | MED9, MED25, mediator complex subunit 9 | ||||||||||||||||||||||||
| External IDs | OMIM: 609878 MGI: 2183151 HomoloGene: 32385 GeneCards: MED9 | ||||||||||||||||||||||||
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| Species | Human | Mouse | |||||||||||||||||||||||
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| Location (UCSC) | Chr 17: 17.48 – 17.49 Mb | n/a | |||||||||||||||||||||||
| PubMed search | [2] | [3] | |||||||||||||||||||||||
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Function
The 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
References
- GRCh38: Ensembl release 89: ENSG00000141026 - 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
This article incorporates text from the United States National Library of Medicine, which is in the public domain.
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