Homo sapiens dual serine/threonine and tyrosine protein kinase (DSTYK) - Nucleotide

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Mouse and human studies support DSTYK loss of function as a low-penetrance and variable expressivity risk factor for congenital urinary tract anomalies. [Genet Med. 2023]
Mouse and human studies support DSTYK loss of function as a low-penetrance and variable expressivity risk factor for congenital urinary tract anomalies.
Martino J, Liu Q, Vukojevic K, Ke J, Lim TY, Khan A, Gupta Y, Perez A, Yan Z, Milo Rasouly H, et al. Genet Med. 2023 Dec; 25(12):100983. Epub 2023 Sep 21.
A central chaperone-like role for 14-3-3 proteins in human cells. [Mol Cell. 2023]
A central chaperone-like role for 14-3-3 proteins in human cells.
Segal D, Maier S, Mastromarco GJ, Qian WW, Nabeel-Shah S, Lee H, Moore G, Lacoste J, Larsen B, Lin ZY, et al. Mol Cell. 2023 Mar 16; 83(6):974-993.e15.
Aberrations in FGFR1, FGFR2, and RIP5 Expression in Human Congenital Anomalies of the Kidney and Urinary Tract (CAKUT). [Int J Mol Sci. 2022]
Aberrations in FGFR1, FGFR2, and RIP5 Expression in Human Congenital Anomalies of the Kidney and Urinary Tract (CAKUT).
Kelam N, Racetin A, Polović M, Benzon B, Ogorevc M, Vukojević K, Glavina Durdov M, Dunatov Huljev A, Kuzmić Prusac I, Čarić D, et al. Int J Mol Sci. 2022 Dec 8; 23(24). Epub 2022 Dec 8.

RefSeq alternative splicing
See 14 reference mRNA sequence splice variants for the DSTYK gene.
RefSeq protein product
See the reference protein sequence for dual serine/threonine and tyrosine protein kinase isoform 2 (NP_955749.1).

Protein
Protein sequence from Nucleotide coding region
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Nucleotide