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...
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FG syndrome (section MED12 gene)
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...
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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...
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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...
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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...
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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...
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higher incidence of phyllodes tumors include Mediator Complex Subunit 12 (MED12) exon 2, Telomerase Reverse Transcriptase (TERT) promoter, and Retinoic...
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MFAP5, TGFB2, SMAD4, MYH11 dominant Feingold syndrome MYCN FG syndrome MED12 FBXW7 neurodevelopmental syndrome FBXW7 Fibular aplasia-ectrodactyly syndrome...
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HGNC:25487 Q9NWA0 9408 MED10 HGNC:28760 Q9BTT4 9409 MED11 HGNC:32687 Q9P086 9410 MED12 HGNC:11957 Q93074 9411 MED12L HGNC:16050 Q86YW9 9412 MED13 HGNC:22474 Q9UHV7...
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many other factors which will affect transcription activation: BAG1, CAV3, MED12, MED24, NCOR1, NCOR2, NCOA2 RXRA, RUNX1, RUNX1T1, SNW1, STAT1, and ZBTB16...
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Oculodentodigital dysplasia 164200 GJA1 Optiz–Kaveggia syndrome 305450 MED12 Otopalatodigital syndrome 2 304120 FLNA Periventricular heterotopia X‐linked...
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modules in regulating T cell effector differentiation and demonstrated that MED12 knockout increased the potency of human T cells in preclinical models. Mackall...
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EP300 ESR2 FOXO1 GREB1 GTF2H1 HSPA1A HSPA8 HSP90AA1 ISL1 JARID1A MVP MED1 MED12 MED14 MED16 MED24 MED6 MGMT MNAT1 MTA1 NCOA6 NCOA1 NCOA2 NCOA3 NRIP1 PDLIM1...
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complex of Mediator proteins (see Figure), especially Mediator subunit 12 (MED12), appears to be essential in forming the chromosome loop that brings the...
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Garraway LA (Jun 2012). "Exome sequencing identifies recurrent SPOP, FOXA1 and MED12 mutations in prostate cancer". Nature Genetics. 44 (6): 685–9. doi:10.1038/ng...
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estrogen-related receptor gamma (ERR-γ). Farnesoid X receptor FBXW7 MED1, MED12, MED14, MED17, NRF1 Peroxisome proliferator-activated receptor gamma Retinoid...
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in males. SOX9 has been shown to interact with steroidogenic factor 1, MED12, MAF, SWI/SNF, MLL3 and MLL4. Loss of function mutations with Sox9 can lead...
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complex. The product of this gene is proposed to form a sub-complex with MED12, cyclin C, and CDK8 that can negatively regulate transactivation by mediator...
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611818; CAV3 Lowe syndrome; 309000; OCRL Lujan–Fryns syndrome; 309520; MED12 Lung cancer; 211980; DLEC1 Lung cancer; 211980; RASSF1 Lung cancer; 211980;...
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THR1 has been shown to interact with: COPS2, EP300, ITGB3BP, MED1, MED6, MED12, MED16, MEF2A, NCOA6, TRIP11, and UBC. GRCh38: Ensembl release 89: ENSG00000126351...
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8 has been shown to interact with: CCNC CREB binding protein CRSP3 MED1 MED12 MED14 MED16 MED17 MED21 MED24 MED26 MED6 Notch proteins POLR2A SMARCB1 STAT1...
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has been shown to interact with MED8, Cyclin-dependent kinase 8, POLR2A, MED12 and MED28. It also acts synergistically to mediate the interaction between...
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Modification of signaling pathways and genes (e.g. CYP1A1, CYP1b1, and MED12) exhibits a correlation with the development and growth of tumors in the...
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