Homo sapiens GTPBP1 full length open reading frame (ORF) cDNA clone (c - Nucleotide

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Bi-allelic genetic variants in the translational GTPases GTPBP1 and GTPBP2 cause a distinct identical neurodevelopmental syndrome. [Am J Hum Genet. 2024]
Bi-allelic genetic variants in the translational GTPases GTPBP1 and GTPBP2 cause a distinct identical neurodevelopmental syndrome.
Salpietro V, Maroofian R, Zaki MS, Wangen J, Ciolfi A, Barresi S, Efthymiou S, Lamaze A, Aughey GN, Al Mutairi F, et al. Am J Hum Genet. 2024 Jan 4; 111(1):200-210. Epub 2023 Dec 20.
Multisite phosphorylation dictates selective E2-E3 pairing as revealed by Ubc8/UBE2H-GID/CTLH assemblies. [Mol Cell. 2024]
Multisite phosphorylation dictates selective E2-E3 pairing as revealed by Ubc8/UBE2H-GID/CTLH assemblies.
Chrustowicz J, Sherpa D, Li J, Langlois CR, Papadopoulou EC, Vu DT, Hehl LA, Karayel Ö, Beier V, von Gronau S, et al. Mol Cell. 2024 Jan 18; 84(2):293-308.e14. Epub 2023 Dec 18.
Antagonistic roles of canonical and Alternative-RPA in disease-associated tandem CAG repeat instability. [Cell. 2023]
Antagonistic roles of canonical and Alternative-RPA in disease-associated tandem CAG repeat instability.
Gall-Duncan T, Luo J, Jurkovic CM, Fischer LA, Fujita K, Deshmukh AL, Harding RJ, Tran S, Mehkary M, Li V, et al. Cell. 2023 Oct 26; 186(22):4898-4919.e25. Epub 2023 Oct 11.

RefSeq alternative splicing
See 15 reference mRNA sequence splice variants for the GTPBP1 gene.

reagents [ExactAntigen/Labome]
reagents
ExactAntigen/Labome
Order full-length cDNA clone [GeneCopoeia Inc.]
Order full-length cDNA clone
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Nucleotide