non-specific lethal 1, isoform L [Drosophila melanogaster]

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Mutations in the chromatin modifier gene KANSL1 cause the 17q21.31 microdeletion syndrome. [Nat Genet. 2012]
Mutations in the chromatin modifier gene KANSL1 cause the 17q21.31 microdeletion syndrome.
Koolen DA, Kramer JM, Neveling K, Nillesen WM, Moore-Barton HL, Elmslie FV, Toutain A, Amiel J, Malan V, Tsai AC, et al. Nat Genet. 2012 Apr 29; 44(6):639-41. Epub 2012 Apr 29.
Tumor suppressor roles of CENP-E and Nsl1 in Drosophila epithelial tissues. [Cell Cycle. 2014]
Tumor suppressor roles of CENP-E and Nsl1 in Drosophila epithelial tissues.
Clemente-Ruiz M, Muzzopappa M, Milán M. Cell Cycle. 2014; 13(9):1450-5. Epub 2014 Mar 10.
Evolutionary conserved NSL complex/BRD4 axis controls transcription activation via histone acetylation. [Nat Commun. 2020]
Evolutionary conserved NSL complex/BRD4 axis controls transcription activation via histone acetylation.
Gaub A, Sheikh BN, Basilicata MF, Vincent M, Nizon M, Colson C, Bird MJ, Bradner JE, Thevenon J, Boutros M, et al. Nat Commun. 2020 May 7; 11(1):2243. Epub 2020 May 7.

RefSeq mRNA
See reference mRNA sequence for the nsl1 gene (NM_001260195.2).
RefSeq protein isoforms
See 12 reference sequence protein isoforms for the nsl1 gene.

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Dryad Digital Repository [Dryad Digital Repository]
Dryad Digital Repository
Ensembl [Ensembl]
Ensembl
GlyGen glycoinformatics resource [GlyGen glycoinformatics resou...]
GlyGen glycoinformatics resource

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Protein