MED9

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

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

AliasesMED9, MED25, mediator complex subunit 9
End17,493,221 bp[1]
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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
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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

Further reading

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