Homo sapiens TSC complex subunit 2 (TSC2), transcript variant 12, 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.
Comparative interactome analysis of α-arrestin families in human and Drosophila. [Elife. 2024]
Comparative interactome analysis of α-arrestin families in human and Drosophila.
Lee KT, Pranoto IKA, Kim SY, Choi HJ, To NB, Chae H, Lee JY, Kim JE, Kwon YV, Nam JW. Elife. 2024 Jan 25; 12. Epub 2024 Jan 25.
The role of TSC1 and TSC2 proteins in neuronal axons. [Mol Psychiatry. 2024]
The role of TSC1 and TSC2 proteins in neuronal axons.
Karalis V, Wood D, Teaney NA, Sahin M. Mol Psychiatry. 2024 Apr; 29(4):1165-1178. Epub 2024 Jan 11.

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 12 (NP_001357334.1).

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.
BioSystems
BioSystems
CCDS
Link to Consensus CDS
Components (Core)
Links to Core components
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Functional Class
Functional class of the sequence domain architecture
Gene
Link to related Genes
OMIM
OMIM records associated with Nucleotide sequence
PubMed (RefSeq)
Link to RefSeq PubMed articles
PubMed (Weighted)
Links to pubmed

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Nucleotide