Homo sapiens selenophosphate synthetase 1, mRNA (cDNA clone MGC:74471 - Nucleotide

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Genome-wide CRISPR screens identify novel regulators of wild-type and mutant p53 stability. [Mol Syst Biol. 2024]
Genome-wide CRISPR screens identify novel regulators of wild-type and mutant p53 stability.
Lü Y, Cho T, Mukherjee S, Suarez CF, Gonzalez-Foutel NS, Malik A, Martinez S, Dervovic D, Oh RH, Langille E, et al. Mol Syst Biol. 2024 Jun; 20(6):719-740. Epub 2024 Apr 5.
De novo missense variants in exon 9 of SEPHS1 cause a neurodevelopmental condition with developmental delay, poor growth, hypotonia, and dysmorphic features. [Am J Hum Genet. 2024]
De novo missense variants in exon 9 of SEPHS1 cause a neurodevelopmental condition with developmental delay, poor growth, hypotonia, and dysmorphic features.
Mullegama SV, Kiernan KA, Torti E, Pavlovsky E, Tilton N, Sekula A, Gao H, Alaimo JT, Engleman K, Rush ET, et al. Am J Hum Genet. 2024 Apr 4; 111(4):778-790. Epub 2024 Mar 25.
TRIM67 drives tumorigenesis in oligodendrogliomas through Rho GTPase-dependent membrane blebbing. [Neuro Oncol. 2023]
TRIM67 drives tumorigenesis in oligodendrogliomas through Rho GTPase-dependent membrane blebbing.
Demirdizen E, Al-Ali R, Narayanan A, Sun X, Varga JP, Steffl B, Brom M, Krunic D, Schmidt C, Schmidt G, et al. Neuro Oncol. 2023 Jun 2; 25(6):1031-1043.

RefSeq alternative splicing
See 10 reference mRNA sequence splice variants for the SEPHS1 gene.

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Nucleotide