Med12 - mediator complex subunit 12-BMKCloudï½ç¾è¿å®¢äº

例如："NBL1", "4681", "drought"

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679693 Med12

基因描述

Type	Description
Definition	mediator complex subunit 12

名称对应

Type	IDs
Gene	UniProtKB-ID: A0A096MKF8_RAT, D3ZDE6_RAT, A0A0G2K4W3_RAT UniprotKB: A0A096MKF8, D3ZDE6, A0A0G2K4W3 UniParc: UPI0000DA4535, UPI0001CF4285, UPI0004E4737A EMBL: AABR07039195 Ensembl: ENSRNOG00000003848 KO: rno:679693
Nucleutide sequences	Ensembl_TRS: ENSRNOT00000076957, ENSRNOT00000040334, ENSRNOT00000090192
Protein sequencees	Ensembl_PRO: ENSRNOP00000068498, ENSRNOP00000048013, ENSRNOP00000073197 RefSeq: XP_008771495.1, XP_006257166.1, NP_001180221.1, XP_008771494.1
Others	UniRef100: UniRef100_A0A096MKF8, UniRef100_A0A0G2K4W3, UniRef100_D3ZDE6 UniRef90: UniRef90_Q93074 UniRef50: UniRef50_Q93074 UniGene: Rn.160193

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mRNA

Protein

UniprotKB

Description

Refseq

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Location

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Pubmed编号	文献信息	发表日期	相关基因
30361391	FMRP recruitment of Î²-catenin to the translation pre-initiation complex represses translation. Saviz Ehyai , Tetsuaki Miyake , Declan Williams , Jyotsna Vinayak , Mark A Bayfield , John C McDermott	2018-12-01	-
26891131	Exome Sequencing of Uterine Leiomyosarcomas Identifies Frequent Mutations in TP53, ATRX, and MED12. PLoS Genet. Netta MÃ¤kinen , Mervi Aavikko , Tuomas Heikkinen , Minna Taipale , Jussi Taipale , Riitta Koivisto-Korander , Ralf BÃ¼tzow , Pia Vahteristo	2016-02-01	-
24039113	Clinical and neurocognitive characterization of a family with a novel MED12 gene frameshift mutation. Am J Med Genet A Gaetan Lesca , Marie-Pierre Moizard , Gerald Bussy , Dominique Boggio , Hao Hu , Stefan A Haas , Hans-Hilger Ropers , Vera M Kalscheuer , Vincent Des Portes , Audrey Labalme , Damien Sanlaville , Patrick Edery , Martine Raynaud , James Lespinasse	2013-12-01	-
24088064	The Mediator complex and transcription regulation. Crit. Rev. Biochem. Mol. Biol. Zachary C Poss , Christopher C Ebmeier , Dylan J Taatjes	2013-10-03	-
23575864	Sox10 cooperates with the mediator subunit 12 during terminal differentiation of myelinating glia. J. Neurosci. Michael R Vogl , Simone Reiprich , Melanie KÃ¼spert , Thomas Kosian , Heinrich Schrewe , Klaus-Armin Nave , Michael Wegner	2013-04-10	-
23395478	Mutations in MED12 cause X-linked Ohdo syndrome. Am. J. Hum. Genet. Anneke T Vulto-van Silfhout , Bert B A de Vries , Bregje W M van Bon , Alexander Hoischen , Martina Ruiterkamp-Versteeg , Christian Gilissen , Fangjian Gao , Marloes van Zwam , Cornelis L Harteveld , Anthonie J van Essen , Ben C J Hamel , Tjitske Kleefstra , MichÃ¨l A A P Willemsen , Helger G Yntema , Hans van Bokhoven , Han G Brunner , Thomas G Boyer , Arjan P M de Brouwer	2013-03-07	-
21873635	Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium. Brief. Bioinformatics Pascale Gaudet , Michael S Livstone , Suzanna E Lewis , Paul D Thomas	2011-09-01	-
20507344	A novel mutation in MED12 causes FG syndrome (Opitz-Kaveggia syndrome). Clin. Genet. P Rump , R C Niessen , K T Verbruggen , O F Brouwer , M de Raad , R Hordijk	2011-02-01	MED12
20720539	Mediator and cohesin connect gene expression and chromatin architecture. Nature Michael H Kagey , Jamie J Newman , Steve Bilodeau , Ye Zhan , David A Orlando , Nynke L van Berkum , Christopher C Ebmeier , Jesse Goossens , Peter B Rahl , Stuart S Levine , Dylan J Taatjes , Job Dekker , Richard A Young	2010-09-23	-
20630950	Med12 is essential for early mouse development and for canonical Wnt and Wnt/PCP signaling. Development Pedro P Rocha , Manuela Scholze , Wilfrid Bleiss , Heinrich Schrewe	2010-08-01	Prickle1, Axin2, Casp3, Ctnnb1, Ccnd1, Cdh1, Cer1, Crabp1, Cyp26a1, Dkk1, Egr2, Fgf17, Fgf8, Fzd3, Hesx1, Il2rg, Lfng, Myc, Otx2, Pax3, Shh, T, Tbx6, Tcf7, Uncx, Wnt5a, Nlgn3, Mixl1, Med12, Vangl2

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