MED12
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Template:Short description Template:Cs1 config Template:Infobox gene Mediator of RNA polymerase II transcription, subunit 12 homolog (S. cerevisiae), also known as MED12, is a human gene found on the X chromosome.[1]
Clinical significance
Mutations in MED12 are responsible for at least two different forms of X-linked dominant mental retardation, Lujan-Fryns syndrome and FG syndrome, as well as instances of prostate cancer.[2]
Mutations in MED12 are associated with uterine leiomyomas[3] and breast fibroepithelial tumors (e.g. fibroadenoma and phyllodes tumors).[4]
Interactions
MED12 has been shown to interact with:
- Calcitriol receptor,[5]
- Cyclin-dependent kinase 8[5][6]
- Estrogen receptor alpha,[6]
- Gli3, G9a, PPARGC1A,[7]
- MED26,[8]
- SOX9,[9] and
- Thyroid hormone receptor alpha.[5]
References
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Further reading
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