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MED12

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維基百科,自由的百科全書
MED12
識別號
別名MED12;, ARC240, CAGH45, FGS1, HOPA, MED12S, OHDOX, OKS, OPA1, TNRC11, TRAP230, mediator complex subunit 12, Kto, HDKR
外部IDOMIM300188 MGI1926212 HomoloGene68441 GeneCardsMED12
相關疾病
FG syndrome、​blepharophimosis-intellectual disability syndrome, MKB type[1]
基因位置(人類
X染色體
染色體X染色體[2]
X染色體
MED12的基因位置
MED12的基因位置
基因座Xq13.1起始71,118,543 bp[2]
終止71,144,103 bp[2]
RNA表達模式




查閱更多表達數據
直系同源
物種人類小鼠
Entrez
Ensembl
UniProt
mRNA​序列

NM_005120

NM_021521

蛋白序列

NP_005111

NP_067496

基因位置​(UCSC)Chr X: 71.12 – 71.14 MbChr X: 100.32 – 100.34 Mb
PubMed​查找[4][5]
維基數據
檢視/編輯人類檢視/編輯小鼠

MED12Mediator of RNA polymerase II transcription, subunit 12 homolog (S. cerevisiae))是在X染色體發現的人類基因[6]

臨床意義

已隱藏部分未翻譯內容,歡迎參與翻譯

MED12基因上的突變與Lujan-Fryns綜合症FG綜合徵X連鎖顯性遺傳智能障礙,以及前列腺癌有關[7]

Mutations in MED12 are associated with uterine leiomyomas[8] and breast fibroepithelial tumors (e.g. fibroadenoma and phyllodes tumors).[9]

相互作用

MED12可與下列蛋白發生相互作用

參考

  1. ^ 與MED12相關的疾病;在維基數據上查看/編輯參考. 
  2. ^ 2.0 2.1 2.2 GRCh38: Ensembl release 89: ENSG00000184634 - Ensembl, May 2017
  3. ^ 3.0 3.1 3.2 GRCm38: Ensembl release 89: ENSMUSG00000079487 - Ensembl, May 2017
  4. ^ Human PubMed Reference:. National Center for Biotechnology Information, U.S. National Library of Medicine. 
  5. ^ Mouse PubMed Reference:. National Center for Biotechnology Information, U.S. National Library of Medicine. 
  6. ^ Entrez Gene: MED12 mediator of RNA polymerase II transcription, subunit 12 homolog (S. cerevisiae). (原始內容存檔於2010-03-07). 
  7. ^ Barbieri CE, Baca SC, Lawrence MS, Demichelis F, Blattner M, Theurillat JP, White TA, Stojanov P, Van Allen E, Stransky N, Nickerson E, Chae SS, Boysen G, Auclair D, Onofrio RC, Park K, Kitabayashi N, MacDonald TY, Sheikh K, Vuong T, Guiducci C, Cibulskis K, Sivachenko A, Carter SL, Saksena G, Voet D, Hussain WM, Ramos AH, Winckler W, Redman MC, Ardlie K, Tewari AK, Mosquera JM, Rupp N, Wild PJ, Moch H, Morrissey C, Nelson PS, Kantoff PW, Gabriel SB, Golub TR, Meyerson M, Lander ES, Getz G, Rubin MA, Garraway LA. Exome sequencing identifies recurrent SPOP, FOXA1 and MED12 mutations in prostate cancer (PDF). Nature Genetics. Jun 2012, 44 (6): 685–9. PMC 3673022可免費查閱. PMID 22610119. doi:10.1038/ng.2279. 
  8. ^ Kämpjärvi K, Park MJ, Mehine M, Kim NH, Clark AD, Bützow R, Böhling T, Böhm J, Mecklin JP, Järvinen H, Tomlinson IP, van der Spuy ZM, Sjöberg J, Boyer TG, Vahteristo P. Mutations in Exon 1 highlight the role of MED12 in uterine leiomyomas. Human Mutation. Sep 2014, 35 (9): 1136–41. PMID 24980722. S2CID 13931280. doi:10.1002/humu.22612. 
  9. ^ Piscuoglio S, Murray M, Fusco N, Marchiò C, Loo FL, Martelotto LG, Schultheis AM, Akram M, Weigelt B, Brogi E, Reis-Filho JS. MED12 somatic mutations in fibroadenomas and phyllodes tumours of the breast. Histopathology. Nov 2015, 67 (5): 719–29. PMC 4996373可免費查閱. PMID 25855048. doi:10.1111/his.12712. 
  10. ^ 10.0 10.1 10.2 Ito M, Yuan CX, Malik S, Gu W, Fondell JD, Yamamura S, Fu ZY, Zhang X, Qin J, Roeder RG. Identity between TRAP and SMCC complexes indicates novel pathways for the function of nuclear receptors and diverse mammalian activators. Molecular Cell. Mar 1999, 3 (3): 361–70. PMID 10198638. doi:10.1016/S1097-2765(00)80463-3可免費查閱. 
  11. ^ Kitagawa H, Fujiki R, Yoshimura K, Mezaki Y, Uematsu Y, Matsui D, Ogawa S, Unno K, Okubo M, Tokita A, Nakagawa T, Ito T, Ishimi Y, Nagasawa H, Matsumoto T, Yanagisawa J, Kato S. The chromatin-remodeling complex WINAC targets a nuclear receptor to promoters and is impaired in Williams syndrome. Cell. Jun 2003, 113 (7): 905–17. PMID 12837248. doi:10.1016/S0092-8674(03)00436-7可免費查閱. 
  12. ^ 12.0 12.1 Kang YK, Guermah M, Yuan CX, Roeder RG. The TRAP/Mediator coactivator complex interacts directly with estrogen receptors alpha and beta through the TRAP220 subunit and directly enhances estrogen receptor function in vitro. Proceedings of the National Academy of Sciences of the United States of America. Mar 2002, 99 (5): 2642–7. Bibcode:2002PNAS...99.2642K. PMC 122401可免費查閱. PMID 11867769. doi:10.1073/pnas.261715899可免費查閱. 
  13. ^ Wallberg AE, Yamamura S, Malik S, Spiegelman BM, Roeder RG. Coordination of p300-mediated chromatin remodeling and TRAP/mediator function through coactivator PGC-1alpha. Molecular Cell. Nov 2003, 12 (5): 1137–49. PMID 14636573. doi:10.1016/S1097-2765(03)00391-5可免費查閱. 
  14. ^ Sato S, Tomomori-Sato C, Parmely TJ, Florens L, Zybailov B, Swanson SK, Banks CA, Jin J, Cai Y, Washburn MP, Conaway JW, Conaway RC. A set of consensus mammalian mediator subunits identified by multidimensional protein identification technology. Molecular Cell. Jun 2004, 14 (5): 685–91. PMID 15175163. doi:10.1016/j.molcel.2004.05.006可免費查閱. 
  15. ^ Zhou R, Bonneaud N, Yuan CX, de Santa Barbara P, Boizet B, Schomber T, Scherer G, Roeder RG, Poulat F, Berta P, Tibor S. SOX9 interacts with a component of the human thyroid hormone receptor-associated protein complex. Nucleic Acids Research. Jul 2002, 30 (14): 3245–52. PMC 135763可免費查閱. PMID 12136106. doi:10.1093/nar/gkf443. 

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