MED28 Gene - Mediator Complex Subunit 28

A component of the Mediator complex involved in transcriptional regulation and linked to cancer and developmental disorders.

Gene Information Card

Symbol MED28
Full Name Mediator Complex Subunit 28
Gene Type Protein coding
Chromosomal Location 4p15.32
NCBI Gene ID 80306 ncbi.nlm.nih.gov/gene/80306
Ensembl ID ENSG00000138668
UniProt ID Q9H204
OMIM ID 610311
HGNC ID 24636
Aliases EG1, magicin, 1500003D12Rik

Description

MED28 encodes a subunit of the Mediator complex, a multiprotein coactivator required for RNA polymerase II transcription. The protein interacts with other Mediator subunits and transcription factors, playing roles in cell proliferation, differentiation, and cytoskeletal organization. MED28 is also known as magicin and has been implicated in cancer and developmental processes.

Disease Associations

Disease category Pathophysiological mechanism Genomic evidence
Breast cancer Overexpression of MED28 promotes cell proliferation and migration; potential oncogenic role PMID: 21573169
Colorectal cancer Upregulation associated with poor prognosis; may enhance Wnt signaling PMID: 25132229
Gastric cancer Increased expression linked to tumor progression and metastasis PMID: 27323883

Expression Profile

Tissue Expression
Tissue nTPM level
Testis 15.2 Medium
Thyroid 12.8 Medium
Prostate 10.5 Medium
Breast 8.3 Low
Colon 7.1 Low
Cell Line Expression
Cell Line nTPM Notes
MCF7 (breast cancer) 12.0 Moderate expression
HCT116 (colorectal cancer) 14.5 Moderate-high expression
HEK293 (embryonic kidney) 9.8 Low-moderate expression
K562 (leukemia) 6.2 Low expression
Data source:Human Protein Atlas(proteinatlas.org)

Mutations & Variants

Hotspot Mutations
Variant Type Frequency Functional Description
c.287A>G (p.Asn96Ser) Missense <0.01% Unknown; rare variant in population databases
c.454C>T (p.Arg152Trp) Missense <0.01% Reported in COSMIC; potential loss of function
c.631_633del (p.Lys211del) In-frame deletion <0.01% Unknown functional effect
Mutation functional classification

Loss of Function (LOF)

No confirmed loss-of-function mutations reported in ClinVar or COSMIC.

Gain of Function (GOF)

Overexpression in several cancers suggests potential gain-of-function role, but no specific activating mutations identified.

Dominant Negative (DN)

No evidence for dominant-negative mutations.

Pathways

• Mediator complex (Reactome: R-HSA-212436)
• Transcriptional regulation by TP53 (Reactome: R-HSA-3700989)
• Wnt signaling pathway (KEGG: hsa04310)

Protein Summary

MED28 is a 178-amino acid protein (20 kDa) that localizes to the nucleus and cytoplasm. It contains a coiled-coil domain and interacts with other Mediator subunits (e.g., MED1, MED24) and cytoskeletal proteins. The protein is involved in transcriptional coactivation and may regulate cell adhesion and migration. Its expression is elevated in several cancers, suggesting a role in tumorigenesis.

Related Products

Product name Cat.No. Species Gene ID
MED28 Knockout HEK293 Cell Line EDJ-KQ51745 Human 80306 Details Get a Quote
MED28 Knockout HeLa Cell Line EDJ-KQ57324 Human 80306 Details Get a Quote
MED28 Knockout A-549 Cell Line EDJ-KQ65830 Human 80306 Details Get a Quote
MED28 Knockout HCT 116 Cell Line EDJ-KQ74254 Human 80306 Details Get a Quote
Contact Us
*
*
*
How did you hear about us: