MED9

MED9
Identifiers
Aliases	MED9, MED25, mediator complex subunit 9
External IDs	MGI: 2183151 HomoloGene: 32385 GeneCards: MED9
Gene location (Human)
Chr.	Chromosome 17 (human)[1]
End	17,493,226 bp[1]
Gene location (Mouse)
Chr.	Chromosome 11 (mouse)[2]
End	59,962,205 bp[2]
Gene ontology
Molecular function	• RNA polymerase II transcription cofactor activity; • protein binding; • transcription cofactor activity;
Cellular component	• mediator complex; • cell nucleus;
Biological process	• regulation of transcription from RNA polymerase II promoter; • regulation of transcription, DNA-templated; • transcription, DNA-templated;
	Sources:Amigo / QuickGO
Orthologs
	55090
	192191
	ENSG00000141026
	ENSMUSG00000061650
	Q9NWA0
	Q8VCS6
	NM_018019
	NM_138675
	NP_060489
	NP_619616
	Wikidata
View/Edit Human	View/Edit Mouse

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

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].

References

1 2 3 GRCh38: Ensembl release 89: ENSG00000141026 - Ensembl, May 2017
1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000061650 - Ensembl, May 2017
↑ "Human PubMed Reference:".
↑ "Mouse PubMed Reference:".
↑ "Entrez Gene: Mediator complex subunit 9". Retrieved 2018-02-06.

MED9

Function

See also

References

Further reading