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.
In-Depth In Vivo Crosslinking in Minutes by a Compact, Membrane-Permeable, and Alkynyl-Enrichable Crosslinker. [Anal Chem. 2022]
In-Depth In Vivo Crosslinking in Minutes by a Compact, Membrane-Permeable, and Alkynyl-Enrichable Crosslinker.
Gao H, Zhao L, Zhong B, Zhang B, Gong Z, Zhao B, Liu Y, Zhao Q, Zhang L, Zhang Y. Anal Chem. 2022 May 31; 94(21):7551-7558. Epub 2022 May 16.
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.

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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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