SIRT2 - sirtuin 2 Gene

Also Known as SIR2; SIR2L; SIR2L2

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 22933

About SIRT2

Cytogenetic location: 19q13.2 Genomic coordinates (GRCh38): 19:38,878,555-38,899,618 (from NCBI)

This gene has 18 transcripts (splice variants), 1 gene allele, 187 orthologues and 6 paralogues. Ubiquitous expression in brain (RPKM 37.1), ovary (RPKM 15.7) and 25 other tissues.

Summary

This gene encodes a member of the Sirtuin family of proteins, homologs to the yeast Sir2 protein. Members of the Sirtuin family are characterized by a Sirtuin core domain and grouped into four classes. The functions of human sirtuins have not yet been determined; however, yeast Sirtuin proteins are known to regulate epigenetic gene silencing and suppress recombination of rDNA. Studies suggest that the human sirtuins may function as intracellular regulatory proteins with mono-ADP-ribosyltransferase activity. The protein encoded by this gene is included in class I of the Sirtuin family. Several transcript variants are resulted from alternative splicing of this gene. [provided by RefSeq, Jul 2010]

SIRT2 Products (7)

mRNA Protein Name
NM_001193286.2 NP_001180215.1 NAD-dependent protein deacetylase sirtuin-2 isoform 3
XM_047438469.1 XP_047294425.1 NAD-dependent protein deacetylase sirtuin-2 isoform X3
NM_030593.3 NP_085096.1 NAD-dependent protein deacetylase sirtuin-2 isoform 2
XM_047438468.1 XP_047294424.1 NAD-dependent protein deacetylase sirtuin-2 isoform X1
NR_034146.1
XM_011526655.2 XP_011524957.1 NAD-dependent protein deacetylase sirtuin-2 isoform X2
NM_012237.4 NP_036369.2 NAD-dependent protein deacetylase sirtuin-2 isoform 1
Molecular Function GO Annotation Evidence References Source
enables DNA-binding transcription factor binding IPI
IPI: Inferred from physical interaction
12887892 GOA
enables NAD+ binding IDA
IDA: Inferred from direct assay
11427894 GOA
enables NAD+-protein poly-ADP-ribosyltransferase activity IDA
IDA: Inferred from direct assay
10381378 GOA
enables NAD-dependent histone H4K16 deacetylase activity IDA
IDA: Inferred from direct assay
16648462 GOA
NOT enables NAD-dependent histone deacetylase activity IDA
IDA: Inferred from direct assay
24177535 GOA
enables NAD-dependent histone deacetylase activity IDA
IDA: Inferred from direct assay
11427894 GOA
enables NAD-dependent protein demyristoylase activity IDA
IDA: Inferred from direct assay
25704306 GOA
enables NAD-dependent protein depalmitoylase activity IDA
IDA: Inferred from direct assay
32103017 GOA
enables NAD-dependent protein lysine deacetylase activity IDA
IDA: Inferred from direct assay
18722353 GOA
enables NAD-dependent protein lysine deacetylase activity IMP
IMP: Inferred from mutant phenotype
24681946 GOA
enables chromatin binding IDA
IDA: Inferred from direct assay
23908241 GOA
enables histone acetyltransferase binding IPI
IPI: Inferred from physical interaction
12887892 GOA
enables histone deacetylase activity IDA
IDA: Inferred from direct assay
17488717 GOA
enables histone deacetylase binding IPI
IPI: Inferred from physical interaction
12620231 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
12697818 GOA
enables protein lysine deacetylase activity IDA
IDA: Inferred from direct assay
17172643 GOA
enables protein lysine deacetylase activity IMP
IMP: Inferred from mutant phenotype
23908241 GOA
NOT enables tubulin deacetylase activity IDA
IDA: Inferred from direct assay
24177535 GOA
enables tubulin deacetylase activity IDA
IDA: Inferred from direct assay
12620231 GOA
enables ubiquitin binding IDA
IDA: Inferred from direct assay
12697818 GOA
enables zinc ion binding IDA
IDA: Inferred from direct assay
11427894 GOA
Biological Process GO Annotation Evidence References Source
involved in cellular response to hypoxia IDA
IDA: Inferred from direct assay
24681946 GOA
involved in epigenetic regulation of gene expression IMP
IMP: Inferred from mutant phenotype
23908241 GOA
involved in negative regulation of DNA-templated transcription IDA
IDA: Inferred from direct assay
12887892 GOA
involved in negative regulation of autophagy IMP
IMP: Inferred from mutant phenotype
20543840 GOA
involved in negative regulation of protein catabolic process IMP
IMP: Inferred from mutant phenotype
20543840 GOA
involved in negative regulation of striated muscle tissue development IDA
IDA: Inferred from direct assay
12887892 GOA
involved in negative regulation of transcription by RNA polymerase II IDA
IDA: Inferred from direct assay
18722353 GOA
involved in negative regulation of transcription by RNA polymerase II IMP
IMP: Inferred from mutant phenotype
24681946 GOA
involved in peptidyl-lysine deacetylation IDA
IDA: Inferred from direct assay
23932781 GOA
involved in positive regulation of fatty acid biosynthetic process IDA
IDA: Inferred from direct assay
23932781 GOA
involved in positive regulation of proteasomal ubiquitin-dependent protein catabolic process IMP
IMP: Inferred from mutant phenotype
24681946 GOA
involved in proteasome-mediated ubiquitin-dependent protein catabolic process IMP
IMP: Inferred from mutant phenotype
21841822 GOA
NOT involved in protein deacetylation IDA
IDA: Inferred from direct assay
24177535 GOA
involved in protein deacetylation IDA
IDA: Inferred from direct assay
20543840 GOA
involved in regulation of cell cycle IMP
IMP: Inferred from mutant phenotype
17726514 GOA
NOT involved in tubulin deacetylation IDA
IDA: Inferred from direct assay
24177535 GOA
involved in tubulin deacetylation IDA
IDA: Inferred from direct assay
18722353 GOA
Cellular Component GO Annotation Evidence References Source
located in centriole IDA
IDA: Inferred from direct assay
17726514 GOA
located in centrosome IDA
IDA: Inferred from direct assay
17488717 GOA
located in chromosome IDA
IDA: Inferred from direct assay
16648462 GOA
located in cytoplasm IDA
IDA: Inferred from direct assay
12697818 GOA
located in cytosol IDA
IDA: Inferred from direct assay
24681946 GOA
located in microtubule IDA
IDA: Inferred from direct assay
12620231 GOA
located in midbody IDA
IDA: Inferred from direct assay
17726514 GOA
located in mitotic spindle IDA
IDA: Inferred from direct assay
17488717 GOA
located in nucleus IDA
IDA: Inferred from direct assay
15213244 GOA
located in spindle IDA
IDA: Inferred from direct assay
17726514 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

SIRT2 Protein Structure

SIR2

SIR2: Sir2 family (84 - 268)

  • 0
  • 100
  • 200
  • 300
  • 389 a.a.
Protein Preferred Names Protein Names

NAD-dependent protein deacetylase sirtuin-2

  • NAD-dependent deacetylase sirtuin-2

  • NAD-dependent protein defatty-acylase sirtuin-2

  • SIR2-like protein 2

  • regulatory protein SIR2 homolog 2

  • silent information regulator 2

  • sir2-related protein type 2

  • sirtuin type 2

SIRT2 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
SIRT2 Q8IXJ6 BUB1B Homo sapiens O60566 24825348
Intra
SIRT2 Q8IXJ6 SHANK3 Homo sapiens Q9BYB0 21653829
Intra
SIRT2 Q8IXJ6 SHANK3 Homo sapiens Q9BYB0 21653829
Intra
SIRT2 Q8IXJ6 G6PD Homo sapiens P11413 24769394
Intra
SIRT2 Q8IXJ6 KAT2B Homo sapiens Q92831 12887892
Intra
SIRT2 Q8IXJ6 RELA Homo sapiens Q04206 21081649
Cross: Cross-species interaction Intra: Intraspecies interaction

SIRT2 Antibodies

Cat. No. Product Name Application Reactivity
HY-P80320 SIRT2 Antibody (YA081) WB, ICC/IF, IP, FC Human, Rat
HY-P85521 SirT2 Antibody (YA5213) WB, ICC/IF Human, Mouse, Rat
HY-P85521A SirT2 Antibody (YA5213)(PBS only) WB, ICC/IF Human, Mouse, Rat

Related Diseases

Diseases Alias
Thrombocytopenia
  • Low Platelet Count

  • Low Platelets

  • Decreased Platelets

  • Platelet Dysfunction Nos

Body Mass Index Quantitative Trait Locus 11
  • OBESITY

  • Obesity, Susceptibility To

  • Leanness, Inherited

  • Obesity, Susceptibility To, Bmiq11

  • Obesity, Mild, Early-Onset

  • Obesity, Association With

  • Obesity, Early-Onset, Susceptibility To

  • Obesity, Severe

  • Obesity, Severe, And Type Ii Diabetes

  • Obesity, Late-Onset

  • BMIQ11

  • Obesity Bmiq11

  • Obesity, Early-Onset

  • Obesity , Susceptibility To

  • Simple Obesity Nos

  • Excess Fat

  • Obesity, Not Elsewhere Classified, Body Mass Index Not Elsewhere Classified

  • Adiposis

Mitochondrial Complex I Deficiency, Nuclear Type 1
  • Mitochondrial Complex I Deficiency

  • Nadh:Q(1) Oxidoreductase Deficiency

  • MC1DN1

  • Nadh-Coenzyme Q Reductase Deficiency

  • Isolated Mitochondrial Respiratory Chain Complex I Deficiency

  • Isolated Nadh-Coenzyme Q Reductase Deficiency

  • Isolated Nadh-Coq Reductase Deficiency

  • Isolated Nadh-Ubiquinone Reductase Deficiency

  • Mitochondrial Nadh Dehydrogenase Component Of Complex I, Deficiency Of

  • Nuclear Type Mitochondrial Complex I Deficiency 1

  • Isolated Complex I Deficiency

  • Complex 1 Mitochondrial Respiratory Chain Deficiency

  • Nadh Coenzyme Q Reductase Deficiency

  • Complex I Mitochondrial Respiratory Chain Deficiency

  • Deficiency Of Mitochondrial Nadh Dehydrogenase Component Of Complex I

  • Nadh:Ubiquinone Oxidoreductase Deficiency

  • Complex I, Mitochondrial Respiratory Chain, Deficiency Of

Wallerian Degeneration
  • Wallerian Degeneration Of The Pyramidal Tract

Monckeberg Arteriosclerosis
  • Monckeberg Medial Calcific Sclerosis

Amyotrophic Lateral Sclerosis 1
  • Amyotrophic Lateral Sclerosis

  • ALS

  • Lou Gehrig Disease

  • Amyotrophic Lateral Sclerosis Type 1

  • Charcot Disease

  • ALS1

  • Amyotrophic Lateral Sclerosis, Susceptibility To

  • Fals

  • Lou Gehrig'S Disease

  • Mnd

  • Motor Neuron Disease

  • Familial Amyotrophic Lateral Sclerosis

  • Amyotrophic Lateral Sclerosis 1, Familial

  • Amyotrophic Lateral Sclerosis 1, Autosomal Dominant

  • Motor Neuron Disease, Bulbar

  • Motor Neurone Disease

  • Amyotrophic Lateral Sclerosis With Dementia

  • Dementia With Amyotrophic Lateral Sclerosis

  • Motor Neuron Disease, Amyotrophic Lateral Sclerosis

  • Sclerosis, Lateral, Amyotrophic

  • Sclerosis, Lateral, Amyotrophic, Type 1

  • Amyotrophic Sclerosis

  • Als - [Amyotrophic Lateral Sclerosis]

  • Wasting Palsy

  • Amyotrophic Paralysis

  • Amyotrophy Lateral Sclerosis

  • Wasting Paralysis

  • Spinal Progressive Amyotrophy

  • Progressive Atrophic Paralysis

Type 2 Diabetes Mellitus
  • Insulin Resistance

  • NIDDM

  • Diabetes Mellitus, Non-Insulin-Dependent

  • Type 2 Diabetes

  • T2D

  • Noninsulin-Dependent Diabetes Mellitus

  • Diabetes Mellitus, Type Ii

  • Maturity-Onset Diabetes

  • Insulin Resistance, Severe, Digenic

  • Diabetes Mellitus, Type 2

  • Diabetes Mellitus, Noninsulin-Dependent

  • Diabetes Mellitus, Noninsulin-Dependent, Association With

  • Diabetes Mellitus, Noninsulin-Dependent, Late Onset

  • Hypertension, Insulin Resistance-Related, Susceptibility To

  • Insulin Resistance, Susceptibility To

  • Non-Insulin-Dependent Diabetes Mellitus

  • Type Ii Diabetes Mellitus

  • Adult-Onset Diabetes Mellitus

  • Maturity-Onset Diabetes Mellitus

  • Diabetes Mellitus Type 2

  • Type Ii Diabetes

  • Type 2 Diabetes Mellitus, Susceptibility To

  • Diabetes, Type 2

  • Diabetes Mellitus, Noninsulin-Dependent, Susceptibility To

  • Diabetes Mellitus, Non-Insulin-Dependent, Susceptibility To

  • Diabetes Mellitus, Type 2, Susceptibility To

  • Diabetes Mellitus, Noninsulin-Dependent, 2

  • Diabetes Mellitus, Type Ii, Susceptibility To

  • Hypertension, Insulin Resistance-Related

  • Adult-Onset Diabetes

  • Aodm

  • Diabetes Mellitus, Adult-Onset

  • Diabetes Mellitus Type Ii

  • Diabetes Mellitus Type 2, Susceptibility To

  • Diabetes, Type Ii, Susceptibility To

  • Diabetes Type 2

  • Diabetes Mellitus

  • Adult Onset Diabetes

  • Maturity Onset Diabetes

  • Nonketotic Diabetes

  • Non-Insulin Dependent Diabetes Mellitus

  • T2dm - [Type 2 Diabetes Mellitus]

  • Niddm - [Non Insulin Dependent Diabetes Mellitus]

  • Dm2

  • Dm Type Ii

  • Diabetic Type 2

  • Insulin Requiring Type 2 Diabetes

  • Noninsulin Dependent Diabetes

  • Non-Insulin-Dependent Diabetes Mellitus Without Complications

  • Diabetes Due To Insulin Secretory Defect

  • Diabetes Mellitus Due To Insulin Secretory Defect

  • Non-Insulin-Dependent Diabetes Of The Young

  • Senile Diabetes

  • Nonketotic Hyperglycaemia

  • Stable Diabetes

Nervous System Disease
  • Abnormality Of The Nervous System

  • Nervous System Diseases

  • Nervous System Disorder

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Bos taurus SIRT2 VGNC VGNC:34631
Felis catus SIRT2 VGNC VGNC:65156
Canis familiaris SIRT2 VGNC VGNC:53983
Rattus norvegicus SIRT2 RGD RGD:621481
Macaca mulatta SIRT2 VGNC VGNC:77219
Mus musculus SIRT2 MGD MGI:1927664
Others SIRT2 NCBI