SIRT2: Sirtuin 2 - A Key Regulator of Aging, Metabolism, and Cancer

Comprehensive gene card for SIRT2, including genomic data, expression, mutations, and disease associations.

Gene Information Card

Symbol SIRT2
Full Name Sirtuin 2
Gene Type Protein coding
Chromosomal Location 19q13.2
NCBI Gene ID 22933 ncbi.nlm.nih.gov/gene/22933
Ensembl ID ENSG00000068903
UniProt ID Q8IXJ6
OMIM ID 604480
HGNC ID 10886
Aliases SIR2L, SIR2L2, SIR2-like 2

Description

SIRT2 is a member of the sirtuin family of NAD-dependent deacetylases, involved in cellular processes such as cell cycle regulation, genome stability, metabolism, and aging. It deacetylates histones and non-histone proteins, including alpha-tubulin and p53, and has been implicated in cancer, neurodegenerative diseases, and metabolic disorders.

Disease Associations

Disease category Pathophysiological mechanism Genomic evidence
Cancer (breast, liver, glioma) SIRT2 deacetylates and stabilizes oncoproteins or tumor suppressors; altered expression promotes proliferation or metastasis. COSMIC, NCBI, ClinVar
Parkinson's disease SIRT2 deacetylates alpha-synuclein and modulates its aggregation; inhibition reduces neurotoxicity. NCBI, OMIM
Metabolic syndrome SIRT2 regulates insulin signaling and lipid metabolism via deacetylation of FOXO1 and other targets. NCBI, UniProt

Expression Profile

Tissue Expression
Tissue nTPM level
Brain 12.5 Medium
Liver 8.3 Low
Breast 6.7 Low
Testis 15.2 Medium
Heart 4.1 Not detected
Cell Line Expression
Cell Line nTPM Notes
HeLa 10.1 Cervical cancer cell line
MCF7 7.8 Breast cancer cell line
HepG2 9.4 Liver cancer cell line
SH-SY5Y 11.2 Neuroblastoma cell line
Data source:Human Protein Atlas(proteinatlas.org)

Mutations & Variants

Hotspot Mutations
Variant Type Frequency Functional Description
c.354G>A (p.Met118Ile) Missense <0.1% Alters deacetylase activity; reported in COSMIC
c.497C>T (p.Thr166Met) Missense <0.1% Found in cancer samples; functional impact unknown
c.1-?_*_del Deletion Rare Loss of function; associated with altered cell cycle
Mutation functional classification

Loss of Function (LOF)

Deletions or missense mutations reducing deacetylase activity may impair cell cycle control and promote genomic instability.

Gain of Function (GOF)

Rare; some missense variants may enhance deacetylase activity, potentially affecting oncogenic pathways.

Dominant Negative (DN)

Not well documented; possible in cases where mutant SIRT2 interferes with wild-type function.

Gene Ontology (GO)

• NAD-dependent histone deacetylase activity (H3K16 specific) • Protein deacetylase activity
• Chromatin binding • Cell cycle
• DNA repair • Microtubule cytoskeleton organization

Pathways

• p53 signaling pathway
• FOXO signaling pathway
• Circadian rhythm
• Longevity regulating pathway

Protein Summary

SIRT2 is a 389-amino acid NAD-dependent deacetylase predominantly cytoplasmic but shuttles to the nucleus. It deacetylates histones (H3K16, H4K16) and non-histone substrates (alpha-tubulin, p53, FOXO1, NF-kB). It regulates cell cycle progression, genomic stability, and metabolic homeostasis. Dysregulation is linked to cancer, neurodegeneration, and aging.

Related Products

Product name Cat.No. Species Gene ID
Sirt2 Knockout MH-S Cell Line EDJ-KQ78173 Mouse 64383 Details Get a Quote
SIRT2 Knockout HEK293 Cell Line EDJ-KQ1129 Human 22933 Details Get a Quote
SIRT2 Knockout A-549 Cell Line EDJ-KQ18084 Human 22933 Details Get a Quote
SIRT2 Knockout HCT 116 Cell Line EDJ-KQ20331 Human 22933 Details Get a Quote
SIRT2 Knockout HeLa Cell Line EDJ-KQ20332 Human 22933 Details Get a Quote

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