Homo sapiens TSC complex subunit 2 (TSC2), transcript variant 4, 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 4 (NP_001070651.1).

Protein
Protein sequence from Nucleotide coding region
PubMed
PubMed articles cited by Nucleotide sequence record
Taxonomy
Taxonomy sequences associated with Nucleotide record
Annotated Genomic
Genomic sequence records that have the current RNA records as annotated features marking the exons of genes.
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BioSystems
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Components (Core)
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Functional Class
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OMIM
OMIM records associated with Nucleotide sequence
PubMed (RefSeq)
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PubMed (Weighted)
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UCSC Genome Browser [UCSC Genome Browser]
UCSC Genome Browser