Homo sapiens mediator complex subunit 11 (MED11), transcript variant 1 - Nucleotide

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A homozygous MED11 C-terminal variant causes a lethal neurodegenerative disease. [Genet Med. 2022]
A homozygous MED11 C-terminal variant causes a lethal neurodegenerative disease.
Calì E, Lin SJ, Rocca C, Sahin Y, Al Shamsi A, El Chehadeh S, Chaabouni M, Mankad K, Galanaki E, Efthymiou S, et al. Genet Med. 2022 Oct; 24(10):2194-2203. Epub 2022 Aug 24.
OpenCell: Endogenous tagging for the cartography of human cellular organization. [Science. 2022]
OpenCell: Endogenous tagging for the cartography of human cellular organization.
Cho NH, Cheveralls KC, Brunner AD, Kim K, Michaelis AC, Raghavan P, Kobayashi H, Savy L, Li JY, Canaj H, et al. Science. 2022 Mar 11; 375(6585):eabi6983. Epub 2022 Mar 11.
CFTR interactome mapping using the mammalian membrane two-hybrid high-throughput screening system. [Mol Syst Biol. 2022]
CFTR interactome mapping using the mammalian membrane two-hybrid high-throughput screening system.
Lim SH, Snider J, Birimberg-Schwartz L, Ip W, Serralha JC, Botelho HM, Lopes-Pacheco M, Pinto MC, Moutaoufik MT, Zilocchi M, et al. Mol Syst Biol. 2022 Feb; 18(2):e10629.

RefSeq alternative splicing
See the other reference mRNA sequence splice variant for the MED11 gene (NM_001305000.2).
RefSeq protein product
See the reference protein sequence for mediator of RNA polymerase II transcription subunit 11 isoform a (NP_001001683.1).

Protein
Protein sequence from Nucleotide coding region
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OMIM
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Order MED11 cDNA clone/Protein/Antibody/RNAi [OriGene]
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Homo sapiens mediator complex subunit 11 (MED11), transcript variant 1, mRNA
Homo sapiens mediator complex subunit 11 (MED11), transcript variant 1, mRNA
gi|1519241667|ref|NM_001001683.4|

Nucleotide

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Nucleotide