MED31
Mediator of RNA polymerase II transcription subunit 31
Also known as: CGI-125, MED31_HUMAN, Soh1
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9Y3C7
- Gene
- MED31
- Ensembl
- ENSG00000108590
- Chromosome
- 17
- Canonical length
- 131 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm
OverviewNCBI Gene
Predicted to enable transcription coregulator activity and ubiquitin protein ligase activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to act upstream of or within limb development and negative regulation of fibroblast proliferation. Located in nucleus. Part of core mediator complex. [provided by Alliance of Genome Resources, Apr 2025]
Canonical amino-acid sequenceUniProt
131 residues, UniProt reviewed canonical sequence.
>Q9Y3C7|MED31
1 MAAAVAMETD DAGNRLRFQL ELEFVQCLAN PNYLNFLAQR GYFKDKAFVN YLKYLLYWKD
61 PEYAKYLKYP QCLHMLELLQ YEHFRKELVN AQCAKFIDEQ QILHWQHYSR KRMRLQQALA
121 EQQQQNNTSG KLocalizationUniProt · AlphaFold · HPA
Whether an antibody against MED31 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)
- 0.37
- Highest tissue expression
- 25 nTPM
Expression across tissuesHPA
Tissue
- epididymis: 25 nTPM
- pituitary gland: 24 nTPM
- esophagus: 24 nTPM
- basal ganglia: 23 nTPM
- hypothalamus: 23 nTPM
- cerebral cortex: 22 nTPM
Single-cell type
- esophageal apical cells: 241 nCPM
- esophageal suprabasal cells: 126 nCPM
- early primary spermatocytes: 124 nCPM
- suprabasal keratinocytes: 119 nCPM
- gastric progenitor cells: 108 nCPM
- late spermatids: 102 nCPM
Immune cell
- basophil: 78 nTPM
- neutrophil: 64 nTPM
- eosinophil: 39 nTPM
- T-reg: 31 nTPM
- gdT-cell: 26 nTPM
- memory CD8 T-cell: 26 nTPM
Brain region
- hypothalamus: 19 nTPM
- basal ganglia: 18 nTPM
- pons: 17 nTPM
- hippocampal formation: 15 nTPM
- midbrain: 15 nTPM
- cerebral cortex: 14 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)
- 1.28
- gnomAD pLI
- 0
- gnomAD missense Z
- 1.32
- DepMap mean gene effect
- -1.47
- DepMap dependency class
- pan
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- limb development
- negative regulation of fibroblast proliferation
- positive regulation of transcription elongation by RNA polymerase II
- positive regulation of transcription initiation by RNA polymerase II
- protein ubiquitination
- regulation of transcription by RNA polymerase II
- RNA polymerase II preinitiation complex assembly
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Mediator complex, subunit Med31
- Mediator of RNA polymerase II, subunit Med31 superfamily
- SOH1
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of MED31 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 MED31 as an antibody target. Whether an autoantibody or antibody against MED31 could matter depends on whether native MED31 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
MED31 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 MED31 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
Loading the interactive Seroatlas protein explorer...