MED9

MED9
Identifiers
Aliases	MED9, MED25, mediator complex subunit 9
External IDs	OMIM: 609878 MGI: 2183151 HomoloGene: 32385 GeneCards: MED9
Gene location (Human) Chr. Chromosome 17 (human)[1] Band 17p11.2 Start 17,476,994 bp[1] End 17,493,221 bp[1]
Gene ontology Molecular function • GO:0001104 transcription coregulator activity • GO:0001948 protein binding Cellular component • mediator complex • nucleus Biological process • regulation of transcription by RNA polymerase II • regulation of transcription, DNA-templated • transcription, DNA-templated Sources:Amigo / QuickGO
Orthologs
Species	Human	Mouse
Entrez	55090	192191
Ensembl	ENSG00000141026	ENSMUSG00000061650
UniProt	Q9NWA0	Q8VCS6
RefSeq (mRNA)	NM_018019	NM_138675
RefSeq (protein)	NP_060489	NP_619616
Location (UCSC)	Chr 17: 17.48 – 17.49 Mb	n/a
PubMed search	[2]	[3]
Wikidata
View/Edit Human View/Edit Mouse

Mediator complex subunit 9 (Med9) is a protein that in humans is encoded by the MED9 gene. ^[4]

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[]

• Mediator

References[]

Further reading[]

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This article incorporates text from the United States National Library of Medicine, which is in the public domain.