MED30
Mediator of RNA polymerase II transcription subunit 30
Also known as: MED30_HUMAN, THRAP6, TRAP25
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q96HR3
- Gene
- MED30
- Ensembl
- ENSG00000164758
- Chromosome
- 8
- Canonical length
- 178 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm
OverviewNCBI Gene
The multiprotein TRAP/Mediator complex facilitates gene expression through a wide variety of transcriptional activators. MED30 is a component of this complex that appears to be metazoan specific (Baek et al., 2002 [PubMed 11909976]).[supplied by OMIM, Nov 2010]
Canonical amino-acid sequenceUniProt
178 residues, UniProt reviewed canonical sequence.
>Q96HR3|MED30
1 MSTPPLAASG MAPGPFAGPQ AQQAAREVNT ASLCRIGQET VQDIVYRTME IFQLLRNMQL
61 PNGVTYHTGT YQDRLTKLQD NLRQLSVLFR KLRLVYDKCN ENCGGMDPIP VEQLIPYVEE
121 DGSKNDDRAG PPRFASEERR EIAEVNKKLK QKNQQLKQIM DQLRNLIWDI NAMLAMRNLocalizationUniProt · AlphaFold · HPA
Whether an antibody against MED30 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)
- 0.52
- Highest tissue expression
- 42 nTPM
Expression across tissuesHPA
Tissue
- bone marrow: 42 nTPM
- thymus: 23 nTPM
- blood vessel: 19 nTPM
- ovary: 19 nTPM
- adipose tissue: 18 nTPM
- breast: 17 nTPM
Single-cell type
- basal keratinocytes: 131 nCPM
- gastric progenitor cells: 108 nCPM
- suprabasal keratinocytes: 101 nCPM
- neutrophil progenitors: 92 nCPM
- extravillous trophoblasts: 91 nCPM
- fallopian tube ciliated cells: 83 nCPM
Immune cell
- eosinophil: 112 nTPM
- neutrophil: 91 nTPM
- plasmacytoid DC: 83 nTPM
- non-classical monocyte: 70 nTPM
- basophil: 65 nTPM
- naive B-cell: 64 nTPM
Brain region
- white matter: 9.1 nTPM
- spinal cord: 6.9 nTPM
- cerebellum: 6.8 nTPM
- basal ganglia: 6.6 nTPM
- medulla oblongata: 6.1 nTPM
- pons: 5.7 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)
- 0.67
- gnomAD pLI
- 0.4
- gnomAD missense Z
- 0.69
- DepMap mean gene effect
- -1.92
- DepMap dependency class
- pan
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 15% 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
- protein ubiquitination
- RNA polymerase II preinitiation complex assembly
- somatic stem cell population maintenance
Molecular functions
- nuclear thyroid hormone receptor binding
- nuclear vitamin D receptor binding
- transcription coactivator activity
- transcription coregulator activity
- ubiquitin protein ligase activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Mediator complex, subunit Med30, metazoa
- Mediator complex subunit 30
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of MED30 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 MED30 as an antibody target. Whether an autoantibody or antibody against MED30 could matter depends on whether native MED30 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
MED30 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 MED30 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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