SIRT7 - sirtuin 7 Gene

Also Known as SIR2L7

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 51547

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
Molecular Function GO Annotation Evidence References 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 References 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 References 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 References
Intra
SIRT7 Q9NRC8 ELK4 Homo sapiens P28324 22722849
Intra
SIRT7 Q9NRC8 ELK4 Homo sapiens P28324 22722849
Intra
SIRT7 Q9NRC8 NRF1 Homo sapiens Q16656 25792330
Intra
SIRT7 Q9NRC8 NRF1 Homo sapiens Q16656 25792330
Cross: Cross-species interaction Intra: Intraspecies interaction

SIRT7 Antibodies

Cat. No. Product Name Application Reactivity
HY-P87072 SIRT7 Antibody (YA6765) WB, ICC/IF, IHC-P, IP, ChIP Human, Mouse, Rat

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