PREDICTED: Mus musculus CCCTC-binding factor (Ctcf), transcript varian - Nucleotide

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CTCF mutation at R567 causes developmental disorders via 3D genome rearrangement and abnormal neurodevelopment. [Nat Commun. 2024]
CTCF mutation at R567 causes developmental disorders via 3D genome rearrangement and abnormal neurodevelopment.
Zhang J, Hu G, Lu Y, Ren H, Huang Y, Wen Y, Ji B, Wang D, Wang H, Liu H, et al. Nat Commun. 2024 Jul 1; 15(1):5524. Epub 2024 Jul 1.
Systematic assessment of ISWI subunits shows that NURF creates local accessibility for CTCF. [Nat Genet. 2024]
Systematic assessment of ISWI subunits shows that NURF creates local accessibility for CTCF.
Iurlaro M, Masoni F, Flyamer IM, Wirbelauer C, Iskar M, Burger L, Giorgetti L, Schübeler D. Nat Genet. 2024 Jun; 56(6):1203-1212. Epub 2024 May 30.
A CTCF-binding site in the Mdm1-Il22-Ifng locus shapes cytokine expression profiles and plays a critical role in early Th1 cell fate specification. [Immunity. 2024]
A CTCF-binding site in the Mdm1-Il22-Ifng locus shapes cytokine expression profiles and plays a critical role in early Th1 cell fate specification.
Liu C, Nagashima H, Fernando N, Bass V, Gopalakrishnan J, Signorella S, Montgomery W, Lim AI, Harrison O, Reich L, et al. Immunity. 2024 May 14; 57(5):1005-1018.e7. Epub 2024 May 1.

RefSeq alternative splicing
See 17 reference mRNA sequence splice variants for the Ctcf gene.
RefSeq protein product
See the reference protein sequence for transcriptional repressor CTCF isoform X5 (XP_036009639.1).

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Protein
Protein sequence from Nucleotide coding region
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Nucleotide