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MED9

From Wikipedia, the free encyclopedia
MED9
Identifiers
AliasesMED9, MED25, mediator complex subunit 9
External IDsOMIM: 609878; MGI: 2183151; HomoloGene: 32385; GeneCards: MED9; OMA:MED9 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_018019

NM_138675

RefSeq (protein)

NP_060489

NP_619616

Location (UCSC)Chr 17: 17.48 – 17.49 MbChr 11: 59.84 – 59.85 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Mediator complex subunit 9 (Med9) is a protein that in humans is encoded by the MED9 gene. [5]

Function

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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

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References

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  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000141026Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000061650Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ "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.