PREDICTED: Homo sapiens nuclear receptor binding SET domain protein 2 - Nucleotide

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Clinical details of individuals with Rauch-Steindl syndrome due to NSD2 truncating variants. [Mol Genet Genomic Med. 2024]
Clinical details of individuals with Rauch-Steindl syndrome due to NSD2 truncating variants.
Nishi E, Yanagi K, Kaname T, Okamoto N. Mol Genet Genomic Med. 2024 Feb; 12(2):e2396.
Decreased NSD2 impairs stromal cell proliferation in human endometrium via reprogramming H3K36me2. [Reproduction. 2024]
Decreased NSD2 impairs stromal cell proliferation in human endometrium via reprogramming H3K36me2.
Qin CM, Wei XW, Wu JY, Liu XQ, Lin Y. Reproduction. 2024 Mar 1; 167(3). Epub 2024 Feb 12.
Antagonistic roles of canonical and Alternative-RPA in disease-associated tandem CAG repeat instability. [Cell. 2023]
Antagonistic roles of canonical and Alternative-RPA in disease-associated tandem CAG repeat instability.
Gall-Duncan T, Luo J, Jurkovic CM, Fischer LA, Fujita K, Deshmukh AL, Harding RJ, Tran S, Mehkary M, Li V, et al. Cell. 2023 Oct 26; 186(22):4898-4919.e25. Epub 2023 Oct 11.

RefSeq alternative splicing
See 29 reference mRNA sequence splice variants for the NSD2 gene.
RefSeq protein product
See the reference protein sequence for histone-lysine N-methyltransferase NSD2 isoform X2 (XP_054206778.1).

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Order WHSC1 cDNA clone/Protein/Antibody/RNAi [OriGene]
Order WHSC1 cDNA clone/Protein/Antibody/RNAi
OriGene
Order Nsd2 cDNA clone/Protein/Antibody/RNAi [OriGene]
Order Nsd2 cDNA clone/Protein/Antibody/RNAi
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Nucleotide