histone-lysine N-methyltransferase SMYD1 isoform 2 [Homo sapiens]

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Lysine Methyltransferase SMYD1 Regulates Myogenesis via skNAC Methylation. [Cells. 2023]
Lysine Methyltransferase SMYD1 Regulates Myogenesis via skNAC Methylation.
Zhu L, Brown MA, Sims RJ, Tiwari GR, Nie H, Mayfield RD, Tucker HO. Cells. 2023 Jun 22; 12(13). Epub 2023 Jun 22.
A de novo mutation of SMYD1 (p.F272L) is responsible for hypertrophic cardiomyopathy in a Chinese patient. [Clin Chem Lab Med. 2019]
A de novo mutation of SMYD1 (p.F272L) is responsible for hypertrophic cardiomyopathy in a Chinese patient.
Fan LL, Ding DB, Huang H, Chen YQ, Jin JY, Xia K, Xiang R. Clin Chem Lab Med. 2019 Mar 26; 57(4):532-539.
SMYD1 is the underlying gene for the AnWj-negative blood group phenotype. [Eur J Haematol. 2018]
SMYD1 is the underlying gene for the AnWj-negative blood group phenotype.
Yahalom V, Pillar N, Zhao Y, Modan S, Fang M, Yosephi L, Asher O, Shinar E, Celniker G, Resnik-Wolf H, et al. Eur J Haematol. 2018 Oct; 101(4):496-501. Epub 2018 Aug 3.

RefSeq mRNA
See reference mRNA sequence for the SMYD1 gene (NM_001330364.2).
RefSeq protein isoforms
See the other reference sequence protein isoform for the SMYD1 gene (NP_938015.1).

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Ensembl [Ensembl]
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GlyGen glycoinformatics resource [GlyGen glycoinformatics resou...]
GlyGen glycoinformatics resource
reagents [ExactAntigen/Labome]
reagents
ExactAntigen/Labome

histone-lysine N-methyltransferase SMYD1 isoform 2 [Homo sapiens]
histone-lysine N-methyltransferase SMYD1 isoform 2 [Homo sapiens]
gi|1060099143|ref|NP_001317293.1|

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