Homo sapiens semaphorin 6B isoform 2 (SEMA6B) mRNA, complete cds

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Progressive myoclonus epilepsies due to SEMA6B mutations. New variants and appraisal of published phenotypes. [Epilepsia Open. 2023]
Progressive myoclonus epilepsies due to SEMA6B mutations. New variants and appraisal of published phenotypes.
Castellotti B, Canafoglia L, Freri E, Tappatà M, Messina G, Magri S, DiFrancesco JC, Fanella M, Di Bonaventura C, Morano A, et al. Epilepsia Open. 2023 Jun; 8(2):645-650. Epub 2023 Feb 9.
A dual-activity topoisomerase complex regulates mRNA translation and turnover. [Nucleic Acids Res. 2022]
A dual-activity topoisomerase complex regulates mRNA translation and turnover.
Su S, Xue Y, Sharov A, Zhang Y, Lee SK, Martindale JL, Li W, Ku WL, Zhao K, De S, et al. Nucleic Acids Res. 2022 Jul 8; 50(12):7013-7033.
SEMA6B variants cause intellectual disability and alter dendritic spine density and axon guidance. [Hum Mol Genet. 2022]
SEMA6B variants cause intellectual disability and alter dendritic spine density and axon guidance.
Cordovado A, Schaettin M, Jeanne M, Panasenkava V, Denommé-Pichon AS, Keren B, Mignot C, Doco-Fenzy M, Rodan L, Ramsey K, et al. Hum Mol Genet. 2022 Sep 29; 31(19):3325-3340.

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Nucleotide