1. Gene
  2. MED28 - mediator complex subunit 28 Gene

MED28 - mediator complex subunit 28 Gene

Homo sapiens

Also known as EG1; magicin; 1500003D12Rik

Gene ID: 80306 | Gene type: protein coding

About MED28

Cytogenetic location: 4p15.32 Genomic coordinates (GRCh38): 4:17,614,641-17,634,105 (from NCBI)

This gene has 4 transcripts (splice variants) and 230 orthologues. Ubiquitous expression in ovary (RPKM 18.1), placenta (RPKM 17.9) and 25 other tissues.

Summary

Predicted to enable actin binding activity. Predicted to act upstream of or within negative regulation of smooth muscle cell differentiation and stem cell population maintenance. Located in nucleoplasm. [provided by Alliance of Genome Resources, Apr 2022]

MED28 Products(1)

mRNA Protein Name
NM_025205.5 NP_079481.2 mediator of RNA polymerase II transcription subunit 28
Gene Ontology
  • Molecular Function
  • Cellular Component
Molecular Function GO Annotation Evidence Reference Source
enables protein binding IPI
IPI: Inferred from physical interaction
10656681 GOA
Cellular Component GO Annotation Evidence Reference Source
part of core mediator complex IPI
IPI: Inferred from physical interaction
24882805 GOA
located in nucleus IDA
IDA: Inferred from direct assay
24882805 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

MED28 Protein Structure

Med28

Med28: Mediator complex subunit 28 (72 - 174)

  • 0
  • 100
  • 178 a.a.
Protein Preferred Names Protein Names

mediator of RNA polymerase II transcription subunit 28

endothelial-derived gene 1

MED28 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra
MED28 Q9H204 NF2 Homo sapiens P35240 15467741
Intra
MED28 Q9H204 NF2 Homo sapiens P35240-1 15467741
Intra
MED28 Q9H204 NF2 Homo sapiens P35240-1 15467741
Intra
MED28 Q9H204 PUF60 Homo sapiens Q9UHX1 25416956
Intra
MED28 Q9H204 PUF60 Homo sapiens Q9UHX1 25416956
Intra
MED28 Q9H204 PUF60 Homo sapiens Q9UHX1
Y2H
21516116
Intra
MED28 Q9H204 CBY2 Homo sapiens Q8NA61-2 32296183
Intra
MED28 Q9H204 CBY2 Homo sapiens Q8NA61-2 32296183
Intra
MED28 Q9H204 LCK Homo sapiens P06239 16899217
Intra
MED28 Q9H204 LCK Homo sapiens P06239 16899217
Intra
MED28 Q9H204 MIIP Homo sapiens Q5JXC2 32296183
Intra
MED28 Q9H204 MIIP Homo sapiens Q5JXC2 32296183
Cross
MED28 Q9H204 Med30 Mus musculus Q9CQI9 24882805
Intra
MED28 Q9H204 MAGI3 Homo sapiens Q5TCQ9 16964398
Intra
MED28 Q9H204 MED17 Homo sapiens Q9NVC6 35271311
Intra
MED28 Q9H204 MED17 Homo sapiens Q9NVC6 33961781
Intra
MED28 Q9H204 MED17 Homo sapiens Q9NVC6 24882805
Intra
MED28 Q9H204 MED27 Homo sapiens Q6P2C8 33961781
Intra
MED28 Q9H204 MED27 Homo sapiens Q6P2C8 35271311
Intra
MED28 Q9H204 MED6 Homo sapiens O75586 33961781
Intra
MED28 Q9H204 MED6 Homo sapiens O75586 35271311
Intra
MED28 Q9H204 MED29 Homo sapiens Q9NX70 35271311
Intra
MED28 Q9H204 MED29 Homo sapiens Q9NX70 33961781
Intra
MED28 Q9H204 MED29 Homo sapiens Q9NX70 24882805
Intra
MED28 Q9H204 MED30 Homo sapiens Q96HR3 33961781
Intra
MED28 Q9H204 MED30 Homo sapiens Q96HR3 32296183
Intra
MED28 Q9H204 MED30 Homo sapiens Q96HR3 32296183
Intra
MED28 Q9H204 MED30 Homo sapiens Q96HR3 35271311
Intra
MED28 Q9H204 MED22 Homo sapiens Q15528 33961781
Intra
MED28 Q9H204 MED22 Homo sapiens Q15528 24882805
Intra
MED28 Q9H204 MED22 Homo sapiens Q15528 35271311
Intra
MED28 Q9H204 GRB2 Homo sapiens P62993 16899217
Intra
MED28 Q9H204 FYN Homo sapiens P06241 16899217
Intra
MED28 Q9H204 FYN Homo sapiens P06241
Y2H
16899217
Intra
MED28 Q9H204 YES1 Homo sapiens P07947 16964398
Intra
MED28 Q9H204 SRC Homo sapiens P12931 16899217
Intra
MED28 Q9H204 SRC Homo sapiens P12931 16964398
Intra
MED28 Q9H204 SRC Homo sapiens P12931 16964398
Intra
MED28 Q9H204 NDRG1 Homo sapiens Q92597 32814053
Intra
MED28 Q9H204 NDRG1 Homo sapiens Q92597 32814053
Intra
MED28 Q9H204 NDRG1 Homo sapiens Q92597 32814053
Cross
MED28 Q9H204 Med8 Mus musculus Q9D7W5 24882805
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Med23

Intellectual Disability, Autosomal Recessive 18

Autosomal Recessive Nonsyndromic Intellectual Disability-18

Neurofibromatosis, Type Ii

Neurofibromatosis 2

Neurofibromatosis, Type 2

NF2

Neurofibromatosis Type Ii

Bilateral Acoustic Neurofibromatosis

Banf

Acn

Central Neurofibromatosis

Neurofibromatosis, Central Type

Acoustic Schwannomas, Bilateral

Acoustic Neurinoma, Bilateral

Bilateral Acoustic Neurinoma

Bilateral Acoustic Schwannomas

Familial Acoustic Neuromas

Neutropenia, Severe Congenital, X-Linked

X-Linked Severe Congenital Neutropenia

XLN

SCNX

Severe Congenital Neutropenia X-Linked

Neutropenia, Congenital, Severe, X-Linked

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Felis catus MED28 VGNC VGNC:107347
Rattus norvegicus MED28 RGD RGD:1305875
Canis familiaris MED28 VGNC VGNC:43135
Macaca mulatta MED28 VGNC VGNC:74569
Mus musculus MED28 MGD MGI:1914249
Bos taurus MED28 VGNC VGNC:31364