12 homolog (S. cerevisiae), also known as MED12, is a human gene found on the X chromosome. Mutations in MED12 are responsible for at least two different...

most common of the types, and is found in the MED12 gene. Known types and affected genes include: The MED12 gene codes for the mediator complex subunit...

attributed to a missense mutation in the MED12 gene. There is currently no treatment or therapy for the underlying MED12 malfunction, and the exact cause of...

harbor mutations in the exon (exon 2) of the mediator complex subunit 12 (MED12) gene. In particular, these mutations are restricted to the stromal component...

80–85% of fibroids have a mutation in the mediator complex subunit 12 (MED12) gene. A syndrome (Reed's syndrome) that causes uterine leiomyomata along...

to regulate gene expression in vivo, and are prevented by mutations in MED12 that produce the human disease FG syndrome. Thus, the structure of a mediator...

MFAP5, TGFB2, SMAD4, MYH11 dominant Feingold syndrome MYCN FG syndrome MED12 FBXW7 neurodevelopmental syndrome FBXW7 Fibular aplasia-ectrodactyly syndrome...

higher incidence of phyllodes tumors include Mediator Complex Subunit 12 (MED12) exon 2, Telomerase Reverse Transcriptase (TERT) promoter, and Retinoic...

HGNC:25487 Q9NWA0 9410 MED10 HGNC:28760 Q9BTT4 9411 MED11 HGNC:32687 Q9P086 9412 MED12 HGNC:11957 Q93074 9413 MED12L HGNC:16050 Q86YW9 9414 MED13 HGNC:22474 Q9UHV7...

Oculodentodigital dysplasia 164200 GJA1 Optiz–Kaveggia syndrome 305450 MED12 Otopalatodigital syndrome 2 304120 FLNA Periventricular heterotopia X‐linked...