Homo sapiens TSC complex subunit 2 (TSC2), transcript variant 20, mRNA

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A large deletion in TSC2 causes tuberous sclerosis complex by dysregulating PI3K/AKT/mTOR signaling pathway. [Gene. 2024]
A large deletion in TSC2 causes tuberous sclerosis complex by dysregulating PI3K/AKT/mTOR signaling pathway.
Fu J, Liang P, Zheng Y, Xu C, Xiong F, Yang F. Gene. 2024 May 30; 909:148312. Epub 2024 Feb 25.
CBAP regulates the function of Akt-associated TSC protein complexes to modulate mTORC1 signaling. [J Biol Chem. 2023]
CBAP regulates the function of Akt-associated TSC protein complexes to modulate mTORC1 signaling.
Liao WT, Chiang YJ, Yang-Yen HF, Hsu LC, Chang ZF, Yen JJY. J Biol Chem. 2023 Dec; 299(12):105455. Epub 2023 Nov 8.
Novel MSH2 and TSC2 variants in a Chinese family with Lynch syndrome and their synergistic impact in urothelial carcinoma. [Transl Res. 2024]
Novel MSH2 and TSC2 variants in a Chinese family with Lynch syndrome and their synergistic impact in urothelial carcinoma.
Li M, Yan X, Liu H, Miao W, Wu W, Zhao Y, Wang C, Liu H. Transl Res. 2024 Mar; 265:26-35. Epub 2023 Oct 31.

RefSeq alternative splicing
See 51 reference mRNA sequence splice variants for the TSC2 gene.
RefSeq protein product
See the reference protein sequence for tuberin isoform 20 (NP_001393602.1).

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Nucleotide