1. Gene
  2. SIRT7 - sirtuin 7 Gene

SIRT7 - sirtuin 7 Gene

Homo sapiens

Also known as SIR2L7

Gene ID: 51547 | Gene type: protein coding

About SIRT7

Cytogenetic location: 17q25.3 Genomic coordinates (GRCh38): 17:81,911,939-81,918,176 (from NCBI)

This gene has 21 transcripts (splice variants), 189 orthologues and 6 paralogues. Ubiquitous expression in stomach (RPKM 8.5), bone marrow (RPKM 8.5) 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 IV of the Sirtuin family. [provided by RefSeq, Jul 2008]

SIRT7 Products(6)

mRNA Protein Name
XM_011523580.2 XP_011521882.1 NAD-dependent protein deacetylase sirtuin-7 isoform X1
XM_047436231.1 XP_047292187.1 NAD-dependent protein deacetylase sirtuin-7 isoform X5
XM_047436229.1 XP_047292185.1 NAD-dependent protein deacetylase sirtuin-7 isoform X3
XM_047436228.1 XP_047292184.1 NAD-dependent protein deacetylase sirtuin-7 isoform X2
XM_047436230.1 XP_047292186.1 NAD-dependent protein deacetylase sirtuin-7 isoform X4
NM_016538.3 NP_057622.1 NAD-dependent protein deacetylase sirtuin-7
Gene Ontology
  • Molecular Function
  • Biological Process
  • Cellular Component
Molecular Function GO Annotation Evidence Reference Source
enables NAD-dependent histone H3K18 deacetylase activity IDA
IDA: Inferred from direct assay
22722849 GOA
enables NAD-dependent histone H3K18 deacetylase activity IMP
IMP: Inferred from mutant phenotype
28655758 GOA
enables NAD-dependent protein lysine deacetylase activity IDA
IDA: Inferred from direct assay
24207024 GOA
enables chromatin binding IDA
IDA: Inferred from direct assay
22722849 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
19174463 GOA
enables protein methyltransferase activity IDA
IDA: Inferred from direct assay
24207024 GOA
enables protein-glutaryllysine deglutarylase activity IDA
IDA: Inferred from direct assay
31542297 GOA
enables protein-succinyllysine desuccinylase activity IDA
IDA: Inferred from direct assay
27436229 GOA
Biological Process GO Annotation Evidence Reference Source
involved in DNA damage response IDA
IDA: Inferred from direct assay
30944854 GOA
involved in DNA repair-dependent chromatin remodeling IDA
IDA: Inferred from direct assay
27436229 GOA
involved in R-loop processing IDA
IDA: Inferred from direct assay
28790157 GOA
involved in negative regulation of phosphatidylinositol 3-kinase/protein kinase B signal transduction IDA
IDA: Inferred from direct assay
28147277 GOA
involved in negative regulation of protein ubiquitination IDA
IDA: Inferred from direct assay
28886238 GOA
involved in negative regulation of transcription by RNA polymerase II IDA
IDA: Inferred from direct assay
22722849 GOA
involved in positive regulation of gluconeogenesis IMP
IMP: Inferred from mutant phenotype
28655758 GOA
involved in positive regulation of rRNA processing IDA
IDA: Inferred from direct assay
26867678 GOA
involved in positive regulation of transcription by RNA polymerase I IDA
IDA: Inferred from direct assay
30540930 GOA
involved in protein deacetylation IDA
IDA: Inferred from direct assay
24207024 GOA
involved in protein deglutarylation IDA
IDA: Inferred from direct assay
31542297 GOA
involved in rRNA transcription IMP
IMP: Inferred from mutant phenotype
19174463 GOA
involved in regulation of DNA repair IDA
IDA: Inferred from direct assay
30944854 GOA
involved in regulation of mitochondrion organization IMP
IMP: Inferred from mutant phenotype
30420520 GOA
involved in regulation of transcription by RNA polymerase II IDA
IDA: Inferred from direct assay
28426094 GOA
involved in regulation of transcription of nucleolar large rRNA by RNA polymerase I IDA
IDA: Inferred from direct assay
24207024 GOA
involved in transcription initiation-coupled chromatin remodeling IDA
IDA: Inferred from direct assay
28655758 GOA
Cellular Component GO Annotation Evidence Reference Source
located in chromatin IDA
IDA: Inferred from direct assay
30944854 GOA
located in nucleolus IDA
IDA: Inferred from direct assay
16079181 GOA
located in nucleolus organizer region IDA
IDA: Inferred from direct assay
19174463 GOA
located in nucleoplasm IDA
IDA: Inferred from direct assay
24207024 GOA
is active in nucleus IDA
IDA: Inferred from direct assay
36646384 GOA
located in nucleus IDA
IDA: Inferred from direct assay
31075303 GOA
located in site of double-strand break IDA
IDA: Inferred from direct assay
27436229 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

SIRT7 Protein Structure

SIR2

SIR2: Sir2 family (141 - 274)

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

NAD-dependent protein deacetylase sirtuin-7

NAD-dependent deacetylase sirtuin-7

NAD-dependent protein deacylase sirtuin-7

SIR2-like protein 7

regulatory protein SIR2 homolog 7

silent mating type information regulation 2, S.cerevisiae, homolog 7

sir2-related protein type 7

sirtuin type 7

SIRT7 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra
SIRT7 Q9NRC8 ELK4 Homo sapiens P28324
Anti Bait CoIP
22722849
Intra
SIRT7 Q9NRC8 ELK4 Homo sapiens P28324
Anti Tag CoIP
22722849
Intra
SIRT7 Q9NRC8 NRF1 Homo sapiens Q16656
Anti Bait CoIP
25792330
Intra
SIRT7 Q9NRC8 NRF1 Homo sapiens Q16656
Anti Tag CoIP
25792330
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
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

Nervous System Disease

Abnormality Of The Nervous System

Nervous System Diseases

Nervous System Disorder

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

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

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

Monckeberg Arteriosclerosis

Monckeberg Medial Calcific Sclerosis

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
Felis catus SIRT7 VGNC VGNC:65161
Canis familiaris SIRT7 VGNC VGNC:46188
Macaca mulatta SIRT7 VGNC VGNC:77487
Mus musculus SIRT7 MGD MGI:2385849
Bos taurus SIRT7 VGNC VGNC:34636
Rattus norvegicus SIRT7 RGD RGD:1305876