MED4
Mediator of RNA polymerase II transcription subunit 4
Also known as: DRIP36, HSPC126, MED4_HUMAN, TRAP36, VDRIP
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9NPJ6
- Gene
- MED4
- Ensembl
- ENSG00000136146
- Chromosome
- 13
- Canonical length
- 270 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm
OverviewNCBI Gene
This gene encodes a component of the Mediator complex. The Mediator complex interacts with DNA-binding gene-specific transcription factors to modulate transcription by RNA polymerase II. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jul 2012]
Canonical amino-acid sequenceUniProt
270 residues, UniProt reviewed canonical sequence.
>Q9NPJ6|MED4
1 MAASSSGEKE KERLGGGLGV AGGNSTRERL LSALEDLEVL SRELIEMLAI SRNQKLLQAG
61 EENQVLELLI HRDGEFQELM KLALNQGKIH HEMQVLEKEV EKRDSDIQQL QKQLKEAEQI
121 LATAVYQAKE KLKSIEKARK GAISSEEIIK YAHRISASNA VCAPLTWVPG DPRRPYPTDL
181 EMRSGLLGQM NNPSTNGVNG HLPGDALAAG RLPDVLAPQY PWQSNDMSMN MLPPNHSSDF
241 LLEPPGHNKE NEDDVEIMST DSSSSSSESDLocalizationUniProt · AlphaFold · HPA
Whether an antibody against MED4 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)
- 0.56
- Highest tissue expression
- 74 nTPM
Expression across tissuesHPA
Tissue
- bone marrow: 74 nTPM
- thymus: 59 nTPM
- tongue: 55 nTPM
- skeletal muscle: 54 nTPM
- testis: 52 nTPM
- tonsil: 52 nTPM
Single-cell type
- late spermatids: 270 nCPM
- differentiating spermatogonia: 207 nCPM
- syncytiotrophoblasts: 178 nCPM
- late primary spermatocytes: 168 nCPM
- megakaryocytes: 167 nCPM
- esophageal apical cells: 164 nCPM
Immune cell
- eosinophil: 107 nTPM
- basophil: 106 nTPM
- T-reg: 102 nTPM
- total PBMC: 91 nTPM
- NK-cell: 87 nTPM
- memory CD4 T-cell: 85 nTPM
Brain region
- cerebellum: 43 nTPM
- white matter: 32 nTPM
- cerebral cortex: 30 nTPM
- pons: 30 nTPM
- hypothalamus: 29 nTPM
- amygdala: 29 nTPM
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)
- 0.79
- gnomAD pLI
- 0.01
- gnomAD missense Z
- 1.02
- DepMap mean gene effect
- -1.28
- DepMap dependency class
- common
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 7% 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
- transcription coregulator activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Mediator complex, subunit Med4
- Vitamin-D-receptor interacting Mediator subunit 4
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of MED4 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 MED4 as an antibody target. Whether an autoantibody or antibody against MED4 could matter depends on whether native MED4 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
MED4 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 MED4 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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