MED16
Mediator of RNA polymerase II transcription subunit 16
Also known as: DRIP92, MED16_HUMAN, THRAP5, TRAP95
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9Y2X0
- Gene
- MED16
- Ensembl
- ENSG00000175221
- Chromosome
- 19
- Canonical length
- 877 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoli
OverviewNCBI Gene
Enables nuclear thyroid hormone receptor binding activity and transcription coactivator activity. Involved in positive regulation of transcription initiation by RNA polymerase II. Located in nucleus. Part of core mediator complex and mediator complex. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
877 residues, UniProt reviewed canonical sequence.
>Q9Y2X0|MED16
1 MCDLRRPAAG GMMDLAYVCE WEKWSKSTHC PSVPLACAWS CRNLIAFTMD LRSDDQDLTR
61 MIHILDTEHP WDLHSIPSEH HEAITCLEWD QSGSRLLSAD ADGQIKCWSM ADHLANSWES
121 SVGSLVEGDP IVALSWLHNG VKLALHVEKS GASSFGEKFS RVKFSPSLTL FGGKPMEGWI
181 AVTVSGLVTV SLLKPSGQVL TSTESLCRLR GRVALADIAF TGGGNIVVAT ADGSSASPVQ
241 FYKVCVSVVS EKCRIDTEIL PSLFMRCTTD LNRKDKFPAI THLKFLARDM SEQVLLCASS
301 QTSSIVECWS LRKEGLPVNN IFQQISPVVG DKQPTILKWR ILSATNDLDR VSAVALPKLP
361 ISLTNTDLKV ASDTQFYPGL GLALAFHDGS VHIVHRLSLQ TMAVFYSSAA PRPVDEPAMK
421 RPRTAGPAVH LKAMQLSWTS LALVGIDSHG KLSVLRLSPS MGHPLEVGLA LRHLLFLLEY
481 CMVTGYDWWD ILLHVQPSMV QSLVEKLHEE YTRQTAALQQ VLSTRILAMK ASLCKLSPCT
541 VTRVCDYHTK LFLIAISSTL KSLLRPHFLN TPDKSPGDRL TEICTKITDV DIDKVMINLK
601 TEEFVLDMNT LQALQQLLQW VGDFVLYLLA SLPNQGSLLR PGHSFLRDGT SLGMLRELMV
661 VIRIWGLLKP SCLPVYTATS DTQDSMSLLF RLLTKLWICC RDEGPASEPD EALVDECCLL
721 PSQLLIPSLD WLPASDGLVS RLQPKQPLRL QFGRAPTLPG SAATLQLDGL ARAPGQPKID
781 HLRRLHLGAC PTEECKACTR CGCVTMLKSP NRTTAVKQWE QRWIKNCLAV EGRGPDACVT
841 SRASEEAPAF VQLGPQSTHH SPRTPRSLDH LHPEDRPLocalizationUniProt · AlphaFold · HPA
Whether an antibody against MED16 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.27
- Highest tissue expression
- 47 nTPM
Expression across tissuesHPA
Tissue
- liver: 47 nTPM
- pancreas: 44 nTPM
- skeletal muscle: 36 nTPM
- prostate: 34 nTPM
- kidney: 34 nTPM
- ovary: 32 nTPM
Single-cell type
- oocytes: 92 nCPM
- platelets: 70 nCPM
- cytotrophoblasts: 57 nCPM
- syncytiotrophoblasts: 55 nCPM
- foveolar cells: 47 nCPM
- migrating cytotrophoblasts: 42 nCPM
Immune cell
- total PBMC: 37 nTPM
- T-reg: 36 nTPM
- memory CD8 T-cell: 30 nTPM
- memory CD4 T-cell: 28 nTPM
- gdT-cell: 28 nTPM
- neutrophil: 26 nTPM
Brain region
- cerebral cortex: 45 nTPM
- basal ganglia: 42 nTPM
- medulla oblongata: 42 nTPM
- amygdala: 40 nTPM
- thalamus: 39 nTPM
- hippocampal formation: 38 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about MED16.
Disease | AllUniProt
Conditions MED16 is implicated in, by any mechanism.
- Guillouet-Gordon syndrome (GGNS) MIM:621220
Disease | GeneticClinVar
17 pathogenic / likely-pathogenic of 288 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
- Guillouet-Gordon syndrome
- Syndromic intellectual disability
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 1.03
- gnomAD pLI
- 0
- gnomAD missense Z
- -1.67
- DepMap mean gene effect
- -0.16
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- positive regulation of DNA-templated transcription
- positive regulation of transcription elongation by RNA polymerase II
- positive regulation of transcription initiation by RNA polymerase II
- regulation of transcription by RNA polymerase II
- RNA polymerase II preinitiation complex assembly
- transcription by RNA polymerase II
Molecular functions
- nuclear thyroid hormone receptor binding
- nuclear vitamin D receptor binding
- transcription coactivator activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
- WD40 repeat
- Soluble quinoprotein glucose/sorbosone dehydrogenase, beta-propeller domain superfamily
- WD40/YVTN repeat-like-containing domain superfamily
- WD40-repeat-containing domain superfamily
- WD domain, G-beta repeat
- Mediator complex, subunit Med16, N-terminal
- Mediator complex, subunit Med16
- Mediator complex subunit 16, C-terminal
- Mediator of RNA polymerase II transcription subunit 16 , central helical bridge
- Mediator complex subunit 16, N-terminal
- Mediator complex subunit 16, central helical bridge
- Mediator complex subunit 16, C-terminal
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of MED16 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads MED16 as an antibody target. Whether an autoantibody or antibody against MED16 could matter depends on whether native MED16 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
MED16 is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label MED16 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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