Homo sapiens SET domain containing 1B, histone lysine methyltransferas - Nucleotide

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Phenotypic spectrum of SETD1B-related disorder: Myoclonic absence seizures and concurrent intellectual disability - Insights from two cases. [Seizure. 2024]
Phenotypic spectrum of SETD1B-related disorder: Myoclonic absence seizures and concurrent intellectual disability - Insights from two cases.
Tiwari R, Viswanathan LG, Chowdary RM, Kenchaiah R, Asranna A, Sinha S. Seizure. 2024 Jan; 114:57-60. Epub 2023 Nov 29.
In Vivo and In Vitro Characterization of the RNA Binding Capacity of SETD1A (KMT2F). [Int J Mol Sci. 2023]
In Vivo and In Vitro Characterization of the RNA Binding Capacity of SETD1A (KMT2F).
Amin HM, Szabo B, Abukhairan R, Zeke A, Kardos J, Schad E, Tantos A. Int J Mol Sci. 2023 Nov 7; 24(22). Epub 2023 Nov 7.
Epigenetic-focused CRISPR/Cas9 screen identifies (absent, small, or homeotic)2-like protein (ASH2L) as a regulator of glioblastoma cell survival. [Cell Commun Signal. 2023]
Epigenetic-focused CRISPR/Cas9 screen identifies (absent, small, or homeotic)2-like protein (ASH2L) as a regulator of glioblastoma cell survival.
Ozyerli-Goknar E, Kala EY, Aksu AC, Bulut I, Cingöz A, Nizamuddin S, Biniossek M, Seker-Polat F, Morova T, Aztekin C, et al. Cell Commun Signal. 2023 Nov 16; 21(1):328. Epub 2023 Nov 16.

RefSeq alternative splicing
See 6 reference mRNA sequence splice variants for the SETD1B gene.
RefSeq protein product
See the reference protein sequence for histone-lysine N-methyltransferase SETD1B (NP_001340274.1).

Protein
Protein sequence from Nucleotide coding region
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Nucleotide