SIRT1 - sirtuin 1 Gene

Also Known as SIR2; SIR2L1; SIR2alpha

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 23411

About SIRT1

Cytogenetic location: 10q21.3 Genomic coordinates (GRCh38): 10:67,884,656-67,918,390 (from NCBI)

This gene has 6 transcripts (splice variants), 156 orthologues and 6 paralogues. Ubiquitous expression in adrenal (RPKM 17.4), testis (RPKM 16.6) 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. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2008]

SIRT1 Products (3)

mRNA Protein Name
NM_001142498.2 NP_001135970.1 NAD-dependent protein deacetylase sirtuin-1 isoform b
NM_001314049.1 NP_001300978.1 NAD-dependent protein deacetylase sirtuin-1 isoform c
NM_012238.5 NP_036370.2 NAD-dependent protein deacetylase sirtuin-1 isoform a
Molecular Function GO Annotation Evidence References Source
enables DNA-binding transcription factor binding IPI
IPI: Inferred from physical interaction
20955178 GOA
enables HLH domain binding IPI
IPI: Inferred from physical interaction
12535671 GOA
enables NAD-dependent histone H3K14 deacetylase activity IDA
IDA: Inferred from direct assay
15469825 GOA
enables NAD-dependent histone H3K9 deacetylase activity IDA
IDA: Inferred from direct assay
15469825 GOA
enables NAD-dependent histone H4K16 deacetylase activity IDA
IDA: Inferred from direct assay
15469825 GOA
enables NAD-dependent histone deacetylase activity IDA
IDA: Inferred from direct assay
12006491 GOA
enables NAD-dependent histone decrotonylase activity IDA
IDA: Inferred from direct assay
28497810 GOA
enables NAD-dependent protein lysine deacetylase activity IDA
IDA: Inferred from direct assay
15692560 GOA
enables NAD-dependent protein lysine deacetylase activity IMP
IMP: Inferred from mutant phenotype
11672523 GOA
enables bHLH transcription factor binding IPI
IPI: Inferred from physical interaction
12535671 GOA
enables deacetylase activity IDA
IDA: Inferred from direct assay
18203716 GOA
enables enzyme binding IPI
IPI: Inferred from physical interaction
23382074 GOA
enables histone H3K deacetylase activity IDA
IDA: Inferred from direct assay
20027304 GOA
enables histone H4K12 deacetylase activity IDA
IDA: Inferred from direct assay
15469825 GOA
enables histone binding IPI
IPI: Inferred from physical interaction
15469825 GOA
enables histone deacetylase activity EXP
EXP: Inferred from Experiment
18485871 GOA
enables identical protein binding IPI
IPI: Inferred from physical interaction
15469825 GOA
enables keratin filament binding IPI
IPI: Inferred from physical interaction
23382074 GOA
enables mitogen-activated protein kinase binding IPI
IPI: Inferred from physical interaction
20027304 GOA
enables nuclear receptor binding IPI
IPI: Inferred from physical interaction
24043310 GOA
enables p53 binding IPI
IPI: Inferred from physical interaction
11672523 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
11672523 GOA
enables protein lysine deacetylase activity IDA
IDA: Inferred from direct assay
19934257 GOA
enables protein lysine deacetylase activity IMP
IMP: Inferred from mutant phenotype
20203304 GOA
enables protein lysine delactylase activity IDA
IDA: Inferred from direct assay
38512451 GOA
enables transcription corepressor activity IDA
IDA: Inferred from direct assay
12535671 GOA
enables transcription corepressor activity IMP
IMP: Inferred from mutant phenotype
17505061 GOA
Biological Process GO Annotation Evidence References Source
involved in DNA damage response IDA
IDA: Inferred from direct assay
18203716 GOA
involved in DNA repair-dependent chromatin remodeling IDA
IDA: Inferred from direct assay
20100829 GOA
involved in UV-damage excision repair IMP
IMP: Inferred from mutant phenotype
20670893 GOA
involved in angiogenesis IDA
IDA: Inferred from direct assay
20620956 GOA
involved in cellular response to glucose starvation IMP
IMP: Inferred from mutant phenotype
18485871 GOA
involved in cellular response to hydrogen peroxide IDA
IDA: Inferred from direct assay
20027304 GOA
involved in cellular response to hypoxia IMP
IMP: Inferred from mutant phenotype
20620956 GOA
involved in cellular response to tumor necrosis factor IDA
IDA: Inferred from direct assay
15152190 GOA
involved in chromatin organization IMP
IMP: Inferred from mutant phenotype
22956909 GOA
involved in circadian regulation of gene expression IMP
IMP: Inferred from mutant phenotype
18662546 GOA
involved in energy homeostasis IMP
IMP: Inferred from mutant phenotype
18485871 GOA
involved in heterochromatin formation IDA
IDA: Inferred from direct assay
15469825 GOA
involved in intrinsic apoptotic signaling pathway in response to DNA damage by p53 class mediator IMP
IMP: Inferred from mutant phenotype
20100829 GOA
involved in maintenance of nucleus location IDA
IDA: Inferred from direct assay
15692560 GOA
involved in negative regulation of DNA damage response, signal transduction by p53 class mediator IDA
IDA: Inferred from direct assay
11672523 GOA
involved in negative regulation of DNA-binding transcription factor activity IDA
IDA: Inferred from direct assay
11672523 GOA
involved in negative regulation of DNA-templated transcription IDA
IDA: Inferred from direct assay
11672523 GOA
involved in negative regulation of DNA-templated transcription IMP
IMP: Inferred from mutant phenotype
18485871 GOA
involved in negative regulation of NF-kappaB transcription factor activity IDA
IDA: Inferred from direct assay
15152190 GOA
involved in negative regulation of TOR signaling IMP
IMP: Inferred from mutant phenotype
20169165 GOA
involved in negative regulation of androgen receptor signaling pathway IMP
IMP: Inferred from mutant phenotype
17505061 GOA
involved in negative regulation of apoptotic process IMP
IMP: Inferred from mutant phenotype
16892051 GOA
involved in negative regulation of attachment of mitotic spindle microtubules to kinetochore IDA
IDA: Inferred from direct assay
30409912 GOA
involved in negative regulation of canonical NF-kappaB signal transduction IDA
IDA: Inferred from direct assay
17680780 GOA
involved in negative regulation of cell cycle IMP
IMP: Inferred from mutant phenotype
18485871 GOA
involved in negative regulation of cellular response to testosterone stimulus IMP
IMP: Inferred from mutant phenotype
17505061 GOA
involved in negative regulation of cellular senescence IDA
IDA: Inferred from direct assay
20203304 GOA
involved in negative regulation of cellular senescence IMP
IMP: Inferred from mutant phenotype
20424141 GOA
involved in negative regulation of gene expression IMP
IMP: Inferred from mutant phenotype
17916362 GOA
involved in negative regulation of helicase activity IDA
IDA: Inferred from direct assay
18203716 GOA
involved in negative regulation of oxidative stress-induced intrinsic apoptotic signaling pathway IMP
IMP: Inferred from mutant phenotype
17317627 GOA
involved in negative regulation of peptidyl-lysine acetylation IDA
IDA: Inferred from direct assay
20100829 GOA
involved in negative regulation of phosphatidylinositol 3-kinase/protein kinase B signal transduction IMP
IMP: Inferred from mutant phenotype
21149730 GOA
involved in negative regulation of phosphorylation IMP
IMP: Inferred from mutant phenotype
17612497 GOA
involved in negative regulation of protein acetylation IMP
IMP: Inferred from mutant phenotype
17916362 GOA
involved in negative regulation of signal transduction by p53 class mediator IDA
IDA: Inferred from direct assay
29681526 GOA
involved in negative regulation of transcription by RNA polymerase II IDA
IDA: Inferred from direct assay
12535671 GOA
involved in negative regulation of transcription by RNA polymerase II IMP
IMP: Inferred from mutant phenotype
17505061 GOA
involved in negative regulation of triglyceride biosynthetic process IDA
IDA: Inferred from direct assay
29765047 GOA
involved in peptidyl-lysine acetylation IMP
IMP: Inferred from mutant phenotype
18004385 GOA
involved in positive regulation of DNA repair IMP
IMP: Inferred from mutant phenotype
19934257 GOA
involved in positive regulation of MHC class II biosynthetic process IDA
IDA: Inferred from direct assay
21890893 GOA
involved in positive regulation of adaptive immune response IDA
IDA: Inferred from direct assay
21890893 GOA
involved in positive regulation of angiogenesis IDA
IDA: Inferred from direct assay
23960241 GOA
involved in positive regulation of angiogenesis IMP
IMP: Inferred from mutant phenotype
20424141 GOA
involved in positive regulation of apoptotic process IDA
IDA: Inferred from direct assay
15152190 GOA
involved in positive regulation of apoptotic process IMP
IMP: Inferred from mutant phenotype
19047049 GOA
involved in positive regulation of blood vessel endothelial cell migration IDA
IDA: Inferred from direct assay
23960241 GOA
involved in positive regulation of cAMP-dependent protein kinase activity IMP
IMP: Inferred from mutant phenotype
18687677 GOA
involved in positive regulation of cell population proliferation IMP
IMP: Inferred from mutant phenotype
21807113 GOA
involved in positive regulation of cellular senescence IDA
IDA: Inferred from direct assay
18687677 GOA
involved in positive regulation of cysteine-type endopeptidase activity involved in apoptotic process IMP
IMP: Inferred from mutant phenotype
19047049 GOA
involved in positive regulation of double-strand break repair IDA
IDA: Inferred from direct assay
32538779 GOA
involved in positive regulation of endothelial cell proliferation IMP
IMP: Inferred from mutant phenotype
20203304 GOA
involved in positive regulation of gluconeogenesis IDA
IDA: Inferred from direct assay
15692560 GOA
involved in positive regulation of insulin receptor signaling pathway IDA
IDA: Inferred from direct assay
21241768 GOA
involved in positive regulation of macroautophagy IDA
IDA: Inferred from direct assay
18296641 GOA
involved in positive regulation of proteasomal ubiquitin-dependent protein catabolic process IMP
IMP: Inferred from mutant phenotype
20203304 GOA
involved in positive regulation of transcription by RNA polymerase II IDA
IDA: Inferred from direct assay
12837246 GOA
involved in proteasome-mediated ubiquitin-dependent protein catabolic process IMP
IMP: Inferred from mutant phenotype
21841822 GOA
involved in protein deacetylation IDA
IDA: Inferred from direct assay
18203716 GOA
involved in protein deacetylation IMP
IMP: Inferred from mutant phenotype
11672523 GOA
involved in protein ubiquitination IDA
IDA: Inferred from direct assay
21841822 GOA
involved in pyrimidine dimer repair by nucleotide-excision repair IMP
IMP: Inferred from mutant phenotype
21149730 GOA
involved in rDNA heterochromatin formation IDA
IDA: Inferred from direct assay
18485871 GOA
involved in rDNA heterochromatin formation IMP
IMP: Inferred from mutant phenotype
18485871 GOA
involved in regulation of apoptotic process IMP
IMP: Inferred from mutant phenotype
19934257 GOA
involved in regulation of cell population proliferation IMP
IMP: Inferred from mutant phenotype
12006491 GOA
involved in regulation of centrosome duplication IDA
IDA: Inferred from direct assay
31722219 GOA
involved in regulation of endodeoxyribonuclease activity IMP
IMP: Inferred from mutant phenotype
19934257 GOA
involved in regulation of mitotic cell cycle IDA
IDA: Inferred from direct assay
15692560 GOA
involved in regulation of transcription by glucose IMP
IMP: Inferred from mutant phenotype
18485871 GOA
involved in response to hydrogen peroxide IDA
IDA: Inferred from direct assay
19934257 GOA
involved in response to oxidative stress IDA
IDA: Inferred from direct assay
14976264 GOA
involved in single strand break repair IMP
IMP: Inferred from mutant phenotype
20097625 GOA
involved in stress-induced premature senescence IMP
IMP: Inferred from mutant phenotype
17916362 GOA
involved in transforming growth factor beta receptor signaling pathway IDA
IDA: Inferred from direct assay
23960241 GOA
Cellular Component GO Annotation Evidence References Source
part of ESC/E(Z) complex IDA
IDA: Inferred from direct assay
15684044 GOA
located in PML body IDA
IDA: Inferred from direct assay
12006491 GOA
located in chromatin IDA
IDA: Inferred from direct assay
17505061 GOA
part of chromatin silencing complex IDA
IDA: Inferred from direct assay
18485871 GOA
NOT located in cytoplasm IDA
IDA: Inferred from direct assay
15469825 GOA
located in cytoplasm IDA
IDA: Inferred from direct assay
20027304 GOA
is active in cytosol IDA
IDA: Inferred from direct assay
20027304 GOA
part of eNoSc complex IPI
IPI: Inferred from physical interaction
18485871 GOA
located in euchromatin IDA
IDA: Inferred from direct assay
15469825 GOA
located in heterochromatin IDA
IDA: Inferred from direct assay
15469825 GOA
located in nuclear envelope IDA
IDA: Inferred from direct assay
15469825 GOA
located in nuclear inner membrane IDA
IDA: Inferred from direct assay
15469825 GOA
NOT located in nucleolus IDA
IDA: Inferred from direct assay
16079181 GOA
located in nucleolus IDA
IDA: Inferred from direct assay
15469825 GOA
located in nucleoplasm IDA
IDA: Inferred from direct assay
16079181 GOA
located in nucleus IDA
IDA: Inferred from direct assay
11672523 GOA
located in rDNA heterochromatin IDA
IDA: Inferred from direct assay
18485871 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

SIRT1 Protein Structure

SIR2

SIR2: Sir2 family (261 - 447)

  • 0
  • 200
  • 400
  • 600
  • 747 a.a.
Protein Preferred Names Protein Names

NAD-dependent protein deacetylase sirtuin-1

  • NAD-dependent protein deacylase sirtuin-1

  • SIR2-like protein 1

  • regulatory protein SIR2 homolog 1

  • sirtuin type 1

SIRT1 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
SIRT1 Q96EB6 APEX1 Homo sapiens P27695 19934257
Intra
SIRT1 Q96EB6 APEX1 Homo sapiens P27695
IF
19934257
Intra
SIRT1 Q96EB6 IRS2 Homo sapiens Q9Y4H2 21241768
Intra
SIRT1 Q96EB6 IRS2 Homo sapiens Q9Y4H2 17901049
Intra
SIRT1 Q96EB6 FOXO1 Homo sapiens Q12778 15692560
Intra
SIRT1 Q96EB6 FOXO1 Homo sapiens Q12778 18235501
Intra
SIRT1 Q96EB6 SETD7 Homo sapiens Q8WTS6 21245319
Cross
SIRT1 Q96EB6 Foxo1 Mus musculus Q9R1E0 22510882
Intra
SIRT1 Q96EB6 MECOM Homo sapiens Q03112 21555002
Intra
SIRT1 Q96EB6 CIITA Homo sapiens P33076 21890893
Intra
SIRT1 Q96EB6 RPTOR Homo sapiens Q8N122 21471201
Intra
SIRT1 Q96EB6 FOXO3 Homo sapiens O43524 15126506
Intra
SIRT1 Q96EB6 FOXO3 Homo sapiens O43524 14976264
Intra
SIRT1 Q96EB6 FOXO3 Homo sapiens O43524 14976264
Intra
SIRT1 Q96EB6 CSAG2 Homo sapiens Q9Y5P2 32761762
Intra
SIRT1 Q96EB6 CSAG2 Homo sapiens Q9Y5P2 32761762
Intra
SIRT1 Q96EB6 CSAG2 Homo sapiens Q9Y5P2 32761762
Intra
SIRT1 Q96EB6 HES1 Homo sapiens Q14469 12535671
Intra
SIRT1 Q96EB6 XPA Homo sapiens P23025 20670893
Intra
SIRT1 Q96EB6 XPA Homo sapiens P23025 20670893
Intra
SIRT1 Q96EB6 AKT1 Homo sapiens P31749 21775285
Intra
SIRT1 Q96EB6 AKT1 Homo sapiens P31749 21775285
Intra
SIRT1 Q96EB6 CSNK2A1 Homo sapiens P68400 21968188
Intra
SIRT1 Q96EB6 CSNK2A1 Homo sapiens P68400 19680552
Intra
SIRT1 Q96EB6 CSNK2A1 Homo sapiens P68400 20439735
Intra
SIRT1 Q96EB6 CSNK2B Homo sapiens P67870
Y2H
21968188
Intra
SIRT1 Q96EB6 CSNK2B Homo sapiens P67870 21968188
Intra
SIRT1 Q96EB6 CSNK2B Homo sapiens P67870 21968188
Cross
SIRT1 Q96EB6 Ncor1 Mus musculus Q60974 15175761
Intra
SIRT1 Q96EB6 SUV39H1 Homo sapiens O43463 18004385
Intra
SIRT1 Q96EB6 SUV39H1 Homo sapiens O43463 18004385
Intra
SIRT1 Q96EB6 XRCC6 Homo sapiens P12956 17334224
Intra
SIRT1 Q96EB6 XRCC6 Homo sapiens P12956 15205477
Intra
SIRT1 Q96EB6 XRCC6 Homo sapiens P12956 15205477
Intra
SIRT1 Q96EB6 CCAR2 Homo sapiens Q8N163 18235501
Intra
SIRT1 Q96EB6 CCAR2 Homo sapiens Q8N163 18235502
Intra
SIRT1 Q96EB6 CCAR2 Homo sapiens Q8N163 18235502
Intra
SIRT1 Q96EB6 CCAR2 Homo sapiens Q8N163 18235502
Intra
SIRT1 Q96EB6 CCAR2 Homo sapiens Q8N163
GMS
18235502
Intra
SIRT1 Q96EB6 CCAR2 Homo sapiens Q8N163 18235501
Intra
SIRT1 Q96EB6 CCAR2 Homo sapiens Q8N163 18235501
Intra
SIRT1 Q96EB6 MTOR Homo sapiens P42345 21471201
Intra
SIRT1 Q96EB6 MTOR Homo sapiens P42345 21471201
Intra
SIRT1 Q96EB6 TP53 Homo sapiens P04637 18235502
Intra
SIRT1 Q96EB6 TP53 Homo sapiens P04637 11672523
Intra
SIRT1 Q96EB6 TP53 Homo sapiens P04637 18235502
Intra
SIRT1 Q96EB6 TP53 Homo sapiens P04637 12006491
Intra
SIRT1 Q96EB6 TP53 Homo sapiens P04637 21245319
Intra
SIRT1 Q96EB6 TP53 Homo sapiens P04637 32761762
Intra
SIRT1 Q96EB6 TP53 Homo sapiens P04637 18235501
Intra
SIRT1 Q96EB6 TP53 Homo sapiens P04637 18235501
Intra
SIRT1 Q96EB6 TP53 Homo sapiens P04637 17964266
Intra
SIRT1 Q96EB6 WRN Homo sapiens Q14191 19343720
Intra
SIRT1 Q96EB6 WRN Homo sapiens Q14191 18203716
Intra
SIRT1 Q96EB6 WRN Homo sapiens Q14191 19343720
Intra
SIRT1 Q96EB6 MAP1LC3B Homo sapiens Q9GZQ8 18296641
Intra
SIRT1 Q96EB6 MAP1LC3B Homo sapiens Q9GZQ8 18296641
Intra
SIRT1 Q96EB6 TP73 Homo sapiens O15350 16998810
Intra
SIRT1 Q96EB6 NR0B2 Homo sapiens Q15466 20375098
Intra
SIRT1 Q96EB6 NR0B2 Homo sapiens Q15466 20375098
Intra
SIRT1 Q96EB6 NR0B2 Homo sapiens Q15466 20375098
Intra
SIRT1 Q96EB6 NMNAT1 Homo sapiens Q9HAN9 19478080
Intra
SIRT1 Q96EB6 HCFC1 Homo sapiens P51610 21909281
Intra
SIRT1 Q96EB6 TSC2 Homo sapiens P49815 20169165
Intra
SIRT1 Q96EB6 RARA Homo sapiens P10276 19934264
Intra
SIRT1 Q96EB6 EP300 Homo sapiens Q09472 19047049
Intra
SIRT1 Q96EB6 EP300 Homo sapiens Q09472 20660480
Intra
SIRT1 Q96EB6 MYC Homo sapiens P01106 21807113
Intra
SIRT1 Q96EB6 MYC Homo sapiens P01106 21807113
Intra
SIRT1 Q96EB6 RPS19BP1 Homo sapiens Q86WX3 17964266
Intra
SIRT1 Q96EB6 RPS19BP1 Homo sapiens Q86WX3 17964266
Intra
SIRT1 Q96EB6 RPS19BP1 Homo sapiens Q86WX3
Y2H
17964266
Intra
SIRT1 Q96EB6 FOXO4 Homo sapiens P98177 15126506
Intra
SIRT1 Q96EB6 E2F1 Homo sapiens Q01094 19188449
Intra
SIRT1 Q96EB6 E2F1 Homo sapiens Q01094 16892051
Intra
SIRT1 Q96EB6 KAT2B Homo sapiens Q92831 19188449
Intra
SIRT1 Q96EB6 KAT2B Homo sapiens Q92831 19188449
Intra
SIRT1 Q96EB6 NBN Homo sapiens O60934 17612497
Intra
SIRT1 Q96EB6 NBN Homo sapiens O60934 17612497
Intra
SIRT1 Q96EB6 NBN Homo sapiens O60934 17612497
Cross
SIRT1 Q96EB6 Pparg Mus musculus P37238 22863012
Cross
SIRT1 Q96EB6 Nr1h3 Mus musculus Q9Z0Y9 17936707
Intra
SIRT1 Q96EB6 NHLH2 Homo sapiens Q02577 22169038
Cross
SIRT1 Q96EB6 Pparg Mus musculus P37238-1 22863012
Cross
SIRT1 Q96EB6 Pparg Mus musculus P37238-1 22863012
Intra
SIRT1 Q96EB6 SNW1 Homo sapiens Q13573
IF
19934264
Intra
SIRT1 Q96EB6 SNW1 Homo sapiens Q13573 19934264
Intra
SIRT1 Q96EB6 SNW1 Homo sapiens Q13573
Y2H
19934264
Intra
SIRT1 Q96EB6 FHL2 Homo sapiens Q14192 15692560
Intra
SIRT1 Q96EB6 TLE1 Homo sapiens Q04724
Y2H
17680780
Intra
SIRT1 Q96EB6 ACACA Homo sapiens Q13085 19343720
Intra
SIRT1 Q96EB6 ACACA Homo sapiens Q13085 19343720
Intra
SIRT1 Q96EB6 DNMT1 Homo sapiens P26358 21947282
Intra
SIRT1 Q96EB6 DNMT1 Homo sapiens P26358 22094255
Intra
SIRT1 Q96EB6 DNMT1 Homo sapiens P26358 21947282
Intra
SIRT1 Q96EB6 DNMT1 Homo sapiens P26358 21947282
Intra
SIRT1 Q96EB6 DNMT1 Homo sapiens P26358 21947282
Intra
SIRT1 Q96EB6 DVL1 Homo sapiens O14640 20439735
Intra
SIRT1 Q96EB6 RELA Homo sapiens Q04206 15152190
Intra
SIRT1 Q96EB6 RELA Homo sapiens Q04206 15152190
Intra
SIRT1 Q96EB6 DVL3 Homo sapiens Q92997 20439735
Intra
SIRT1 Q96EB6 DVL3 Homo sapiens Q92997 20439735
Intra
SIRT1 Q96EB6 PPARG Homo sapiens P37231 20660480
Intra
SIRT1 Q96EB6 PPARG Homo sapiens P37231 20660480
Intra
SIRT1 Q96EB6 PPARG Homo sapiens P37231 20660480
Intra
SIRT1 Q96EB6 PIK3R1 Homo sapiens P27986 21241768
Intra
SIRT1 Q96EB6 MYCN Homo sapiens P04198 21698133
Intra
SIRT1 Q96EB6 SREBF1 Homo sapiens P36956-3 20817729
Intra
SIRT1 Q96EB6 SREBF1 Homo sapiens P36956-3 20817729
Intra
SIRT1 Q96EB6 ATG7 Homo sapiens O95352 18296641
Intra
SIRT1 Q96EB6 ATG7 Homo sapiens O95352 18296641
Cross: Cross-species interaction Intra: Intraspecies interaction

Recombinant SIRT1 Proteins

Cat. No. Product Name Accession Purity
HY-P71596 SIRT1 Protein, Human (His) Q96EB6-1 (A2-S747) ≥ 90%, as determined by reducing SDS-PAGE.

SIRT1 Antibodies

Cat. No. Product Name Application Reactivity
HY-P80319 SIRT1 Antibody (YA082) WB, IHC-P, ICC/IF, ChIP Human, Mouse
HY-P81303 Phospho-SIRT1 (Ser47) Antibody (YA1036) WB, IHC-P, ICC/IF Human
HY-P81303A Phospho-SIRT1 (Thr530) Antibody (YA1037) WB Human
HY-P84728 SIRT1 Antibody (YA4425) WB, IHC-P, ICC/IF, FC, ELISA Human, Mouse, Rat, Rabbit, Monkey
HY-P84728A SIRT1 Antibody (YA4425)(PBS only) WB, IHC-P, ICC/IF, FC, ELISA Human, Mouse, Rat, Rabbit, Monkey
HY-P86635 SIRT1 Antibody (YA6327) WB, IHC-P, ICC/IF, IP, ELISA Human, Rat

Related Diseases

Diseases Alias
Neuroblastoma
  • Nb

  • Neuroblastoma, Susceptibility To

  • Neuroblastomas

  • Central Neuroblastoma

Osteonecrosis Of The Jaw
Aging
Non-Syndromic X-Linked Intellectual Disability
  • X-Linked Non-Syndromic Intellectual Disability

  • Non-Specific X-Linked Mental Retardation

  • X-Linked Non-Specific Intellectual Disability

Diabetic Encephalopathy
Prostate Cancer
  • Prostate Carcinoma

  • Prostate Cancer, Familial

  • Prostate Neoplasm

  • Prostate Cancer, Somatic

  • Prostate Cancer, Susceptibility To

  • Prostatic Cancer

  • Prostatic Neoplasms

  • Hereditary Prostate Cancer

  • Prostatic Neoplasm

  • Cancer Of Prostate

  • Carcinoma Of Prostate

  • Familial Prostate Cancer

  • Familial Prostate Carcinoma

  • Malignant Tumor Of Prostate

  • Malignant Neoplasm Of Prostate

  • Prostate Cancer, Familial, Susceptibility To

  • Malignant Tumor Of The Prostate

  • Ngp - New Growth Of Prostate

  • Tumor Of The Prostate

  • Prostate Cancer, Hereditary

  • Cancer Of The Prostate

  • Malignant Neoplasm Of The Prostate

  • Prostatic Carcinoma

  • PC

  • Prca

  • Cancer, Prostate

  • Malignant Prostatic Tumour

  • Malignant Tumour Of Prostate

  • Primary Prostate Cancer

  • Primary Malignant Neoplasm Of Prostate

  • Prostate Gland Cancer

Pulpitis
  • Pulp Stones

  • Pulpitis Nos

Fatty Liver Disease
  • Alcoholic Fatty Liver

  • Fatty Liver

  • Fatty Liver, Alcoholic

  • Fatty Change Of Liver

  • Hepatic Lipidosis

  • Steatosis Of Liver

  • Fatty Liver Alcoholic

  • Steatohepatitis

  • Etoh Fatty Liver

  • Etoh Fatty Liver Metamorphosis

  • Fatty Etoh Liver Necrosis

Cataract
  • Cataracts

  • Cat - [Cataract]

  • Cataract Form

  • Lens Opacity

  • Lens Opacities

Non-Alcoholic Steatohepatitis
  • Nonalcoholic Steatohepatitis

  • Nash

  • Nash - [Non-Alcoholic Steatohepatitis]

  • Non-Alcoholic Steatohepatosis

Myopathy
  • Muscular Diseases

  • Myopathies

Acquired Metabolic Disease
Colorectal Cancer
  • Colon Cancer

  • Colorectal Carcinoma

  • Colon Carcinoma

  • Colorectal Cancer, Susceptibility To

  • Carcinoma Of Colon

  • CRC

  • Colorectal Cancer With Chromosomal Instability, Somatic

  • Colon Cancer, Somatic

  • Colon Cancer, Susceptibility To

  • Colonic Neoplasms

  • Colorectal Neoplasms

  • Colorectal Cancer, Somatic

  • Colon Cancer, Advanced, Somatic

  • Colonic Carcinoma

  • Colorectal Carcinomas

  • Colon Cancers

  • Colorectal Cancers

  • Cancer, Colorectal, Somatic

  • Cancer, Colon

  • Cancer, Colorectal, Susceptibility To

  • Colorectal Neoplasm

  • Colonic Neoplasm

  • Malignant Tumor Of Colon

Overnutrition
Cardiovascular System Disease
  • Abnormality Of The Cardiovascular System

  • Disease Of Subdivision Of Hemolymphoid System

  • Disorder Of Cardiovascular System

  • Cardiovascular Diseases

  • Cardiovascular Disease

Werner Syndrome
  • Werner'S Syndrome

  • WRN

  • Adult Progeria

  • Ws

  • Adult Premature Ageing Syndrome

  • Adult Premature Aging Syndrome

  • Werners Syndrome

Dilated Cardiomyopathy
  • Familial Dilated Cardiomyopathy

  • Primary Dilated Cardiomyopathy

  • Idiopathic Dilated Cardiomyopathy

  • Congestive Cardiomyopathy

  • Idiopathic Dilation Cardiomyopathy

  • Primary Familial Dilated Cardiomyopathy

  • Cardiomyopathy, Dilated

  • DCM

  • Cardiomyopathy, Familial Dilated

  • Dilated Cardiomyopathy, Familial

  • Hypokinetic Dilated Cardiomyopathy, Familial

  • Familial Idiopathic Cardiomyopathy

  • Fdc

  • Cardiomyopathy, Familial Idiopathic

  • Idiopathic Cardiomegaly

  • Dilated Congestive Cardiomyopathy

  • Chronic Dilated Cardiomyopathy

  • Ccm - [Congestive Cardiomyopathy]

  • Cocm - [Congestive Cardiomyopathy]

  • Dcm - [Dilated Cardiomyopathy]

  • Dilated-Hypokinetic Cardiomyopathy

  • Congestive Idiopathic Cardiomyopathy

  • Primary Idiopathic Dilated Cardiomyopathy

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

Breast Cancer
  • Breast Carcinoma

  • Breast Cancer, Familial

  • Malignant Neoplasm Of Breast

  • Male Breast Cancer

  • Breast Cancer, Susceptibility To

  • Breast Cancer, Early-Onset

  • Malignant Tumor Of Breast

  • Carcinoma Of Male Breast

  • Breast Cancer, Invasive Ductal

  • Breast Cancer, Protection Against

  • Breast Cancer, Somatic

  • Breast Cancer, Male

  • Breast Cancer, Lobular, Somatic

  • Breast Tumor

  • Mammary Cancer

  • Mammary Tumor

  • Malignant Neoplasm Of Male Breast

  • Mammary Carcinoma

  • Male Breast Carcinoma

  • Familial Cancer Of Breast

  • Invasive Ductal Breast Carcinoma

  • Breast Cancer Susceptibility

  • Breast Cancer, Male, Susceptibility To

  • Breast Cancer, Early-Onset, Susceptibility To

  • Malignant Tumor Of The Breast

  • Mammary Neoplasm

  • Primary Breast Cancer

  • Neoplasm Of Male Breast

  • Carcinoma Of Breast

  • Breast Cancer In Men

  • Familial Breast Cancer

  • Cancer Of Breast

  • BC

  • Breast Cancer Familial

  • Breast Cancer Familial Male

  • Breast Cancer, Familial Male

  • Breast Male Carcinoma

  • Breast Neoplasms

  • Breast Neoplasms, Male

  • Mammary Tumors

  • Mammary Carcinomas

  • Cancer, Breast

  • Cancer, Breast, Susceptibility

  • Invasive Breast Ductal Carcinoma

  • Breast Neoplasm

  • Susceptibility To Breast Cancer

  • Mammary Neoplasms

  • Animal Mammary Neoplasms

  • Primary Malignant Neoplasm Of Breast

  • Infiltrating Ductal Carcinoma Of Breast

  • Infiltrating Duct Carcinoma Of Unspecified Site

  • Infiltrating Ductular Carcinoma Of Unspecified Site

  • Invasive Breast Carcinoma Of No Special Type

  • Microinvasive Carcinoma Of Breast

  • Carcinoma With Apocrine Differentiation

Retinoblastoma
  • RB

  • Trilateral Retinoblastoma

  • RB1

  • Retinoblastoma, Trilateral

  • Neuroblastoma Of Retina

  • Rb - Retinoblastoma

  • Eye Cancer, Retinoblastoma

  • Retinal Cancer

  • Retinal Tumor

  • Glioma, Retinal

  • Non-Hereditary Retinoblastoma

  • Childhood Cancer Retinoblastoma

  • Malignant Neoplasm Of Retina

  • Retinal Neoplasms

Periapical Periodontitis
  • Apical Periodontitis

  • Periodontitis Apical

Eye Disease
  • Eye Diseases

  • Abnormality Of The Eye

  • Toxoplasma Oculopathy

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

Huntington Disease
  • Huntington'S Disease

  • Huntington Chorea

  • HD

  • Huntington'S Chorea

  • Huntington Chronic Progressive Hereditary Chorea

  • Juvenile Huntington Disease

  • Chronic Progressive Chorea

  • Chronic Progressive Hereditary Chorea

  • Hc - [Huntington Chorea]

  • Hereditary Chorea

  • Progressive Hereditary Chorea

Retinitis Pigmentosa
  • RP

  • Rod-Cone Dystrophy

  • Autosomal Recessive Retinitis Pigmentosa

  • Non-Syndromic Retinitis Pigmentosa

  • Pericentral Pigmentary Retinopathy

  • Pigmentary Retinopathy

  • Tapetoretinal Degeneration

  • Rcd

  • Retinitis Pigmentosa Autosomal Recessive

  • ARRP

  • Retinitis Pigmentosa, Autosomal Recessive

  • Retinitis Pigmentosa 1

Alzheimer Disease, Familial, 1
  • Alzheimer Disease

  • Alzheimer'S Disease

  • Presenile And Senile Dementia

  • AD1

  • Alzheimer Disease, Susceptibility To

  • Alzheimer Disease, Late-Onset, Susceptibility To

  • Alzheimer Disease 1, Familial

  • AD

  • Familial Alzheimer Disease

  • Alzheimer Disease, Late-Onset

  • Alzheimers Dementia

  • Alzheimer Dementia

  • Alzheimer Sclerosis

  • Alzheimer Syndrome

  • Alzheimer-Type Dementia

  • Dat

  • Primary Senile Degenerative Dementia

  • Sdat

  • Alzheimer Disease 1

  • Autosomal Dominant Alzheimer Disease

  • Early-Onset Alzheimer Disease With Cerebral Amyloid Angiopathy

  • Late Onset Alzheimer Disease

  • Alzheimers Disease

  • Alzheimer Disease, Early-Onset, With Cerebral Amyloid Angiopathy

  • Late-Onset Alzheimers Disease

  • Alzheimer'S Disease Pathway Kegg

  • Dementia Due To Alzheimer'S Disease

  • Alzheimer Disease Type 1

  • Alzheimers

Osteoporosis
  • Postmenopausal Osteoporosis

  • Osteoporosis, Postmenopausal

  • Bone Mineral Density Quantitative Trait Locus

  • Bmnd

  • Osteoporosis, Involutional

  • Osteoporosis, Susceptibility To

  • Osteoporosis, Postmenopausal, Susceptibility

  • Bone Mineral Density Variation Qtl, Osteoporosis

  • OSTEOP

  • Involutional Osteoporosis

  • Senile Osteoporosis

  • Osteoporosis Postmenopausal

  • Bone Mineral Density, Quantitative Trait Locus

  • Osteoporosis, Senile

  • Idiopathic Osteoporosis

  • Bone Rarefaction Nos

  • Type 1 Osteoporosis

Inclusion Body Myositis
  • Ibm

  • Sporadic Inclusion Body Myositis

  • Myositis, Inclusion Body

  • Inflammatory Myopathy

  • Inflammatory Myopathies

  • Sibm

  • Myositis Inclusion Body

  • Nonaka Myopathy

  • Inclusion Body Myopathy, Autosomal Recessive

  • Inclusion Body Myopathy, Autosomal Dominant

  • Myositis

  • Inclusion Body Myopathy, Sporadic

Hypertension, Essential
  • Essential Hypertension

  • Hypertension

  • High Blood Pressure

  • Hypertension, Essential, Susceptibility To

  • Hypertensive Disease

  • Primary Hypertension

  • EHT

  • Hypertension, Salt-Sensitive Essential, Susceptibility To

  • Hyperpiesia

  • Idiopathic Hypertension

  • Hypertensive Disorder

  • Hypertension, Essential, Susceptibility To, 3

  • Hypertension, Essential 3

  • Hypertension, Essential, Salt-Sensitive

  • Hypertension, Essential, Susceptibility To, 6

  • Hypertension, Essential 6

  • Hypertension, Salt-Sensitive Essential

  • Hypertension, Susceptibility To

  • Hypertension, Essential, Susceptibility To, 4

  • Hypertension, Essential 4

  • Hypertension, Essential, Susceptibility To, 2

  • Hypertension, Essential 2

  • Hypertension, Essential, Susceptibility To, 1

  • Hypertension, Essential 1

  • Hypertension, Essential, Susceptibility To, 5

  • Hypertension, Essential 5

  • Htn

  • Vascular Hypertensive Disorder

  • Systemic Primary Arterial Hypertension

  • Hbp - [High Blood Pressure]

  • Systemic Arterial Hypertensive Disorder

  • Elevated Blood Pressure

  • Arterial Hypertension Nos

  • Hypertension Nos

  • Benign Hypertension

  • Systemic Arterial Hypertension

  • Systemic Hypertension

  • Artery Htn

  • Benign Htn

  • Vascular Htn

  • Vascular Hypertension

  • Cholesterol Hypertension

  • Cholesterol Htn

  • Idiopathic Htn

  • Malignant Hypertension

  • Malignant Htn

  • Raised Blood Pressure

  • Cardiovascular Hypertension

  • Primary Htn - [Hypertension]

  • High Arterial Tension

  • High Blood Pressure Disorder

  • Ht - [Hypertension]

  • Htn - [Hypertension]

  • Hypertensive Vascular Disease

  • Hypertensive Vascular Degeneration

Cockayne Syndrome
  • Cockayne'S Syndrome

  • Dwarfism-Retinal Atrophy-Deafness Syndrome

  • Neill-Dingwall Syndrome

  • Progeria-Like Syndrome

  • Progeroid Nanism

  • Cs

Nervous System Disease
  • Abnormality Of The Nervous System

  • Nervous System Diseases

  • Nervous System Disorder

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

Stroke, Ischemic
  • Cerebral Infarction

  • Stroke

  • Ischemic Stroke

  • Cerebrovascular Accident

  • Cerebral Infarction, Susceptibility To

  • Stroke, Ischemic, Susceptibility To

  • Cerebral Infarct

  • Ischemic Stroke, Susceptibility To

  • Stroke, Susceptibility To

  • Cva - Cerebral Infarction

  • ISCHSTR

  • Ischemic Cerebrovascular Accident

Interstitial Lung Disease 2
  • Idiopathic Pulmonary Fibrosis

  • Ipf

  • Fibrocystic Pulmonary Dysplasia

  • Pulmonary Fibrosis, Idiopathic

  • Pulmonary Fibrosis, Idiopathic, Susceptibility To

  • ILD2

  • Idiopathic Pulmonary Fibrosis, Familial

  • Fibrosing Alveolitis, Cryptogenic

  • Uip

  • Cryptogenic Fibrosing Alveolitis

  • Fibrosing Alveolitis

  • Interstitial Pneumonitis, Usual

  • Familial Idiopathic Pulmonary Fibrosis

  • Idiopathic Fibrosing Alveolitis, Chronic Form

  • Usual Interstitial Pneumonia

  • Fibrosing Alveolitis Cryptogenic

  • Hamman-Rich Disease

  • Idiopathic Pulmonary Fibrosis Familial

  • Interstitial Pneumonitis Usual

  • Fibrosis Idiopathic Pulmonary

  • Fibrosis, Pulmonary, Idiopathic

  • Hamman-Rich Syndrome

  • Chronic Idiopathic Pulmonary Fibrosis

  • Acute Interstitial Pneumonia

  • Interstitial Pulmonary Fibrosis

  • Ipf - [Idiopathic Pulmonary Fibrosis]

  • Idiopathic Lung Fibrosis

  • Fibrosing Lung Disease

  • Pulmonary Fibrosis Nos

  • Fibrosing Pneumonitis

Medulloblastoma
  • MDB

  • Cpnet

  • Localized Primitive Neuroectodermal Tumor

  • Classic Medulloblastoma

  • Desmoplastic/Nodular Medulloblastoma

  • Medulloblastoma With Extensive Nodularity

  • Desmoplastic Medulloblastoma

  • Medulloblastoma, Somatic

  • Medulloblastoma, Desmoplastic

  • Brain Medulloblastoma

  • Cns Pnet

  • Infratentorial Primitive Neuroectodermal Tumor

  • Mben

  • Medulloblastoma Desmoplastic

  • Neuroectodermal Tumors, Primitive

  • Medulloblastomas

  • Medulloblastoma, With Extensive Nodularity

  • Medulloblastoma Of Unspecified Site

  • Medullomyoblastoma Of Unspecified Site

Diabetes Mellitus
  • Diabetes

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

Hyperphosphatemia
Non-Alcoholic Fatty Liver Disease
  • Fatty Liver

  • Non-Alcoholic Fatty Liver

  • Nafld

  • Nonalcoholic Fatty Liver Disease

  • Nonalcoholic Steatohepatitis

  • Steatosis

  • Nafl

  • Nash

  • Non-Alcoholic Steatohepatitis

  • Susceptibility To Nonalcoholic Fatty Liver Disease

  • Steatohepatitis

  • Fatty Degeneration

  • Non-Alcoholic Fatty Liver Disease Without Mention Of Non-Alcoholic Steatohepatitis

  • Nafld Without Nash

  • Nafld Without Mention Of Nash

Laron Syndrome
  • Growth Hormone Insensitivity Syndrome

  • Growth Hormone Receptor Deficiency

  • Laron Dwarfism

  • Pituitary Dwarfism Ii

  • Laron-Type Isolated Somatotropin Defect

  • Primary Growth Hormone Resistance

  • Laron-Type Dwarfism

  • Laron Type Pituitary Dwarfism I

  • Primary Growth Hormone Insensitivity

  • Primary Gh Resistance

  • Gh-R Deficiency

  • Growth Hormone Receptor Defect

  • Laron-Type Pituitary Dwarfism

  • Laron-Type Short Stature

  • Severe Gh Insensitivity

  • Ghis

  • Short Stature Due To A Defect In Growth Hormone Receptor Or Post-Receptor Pathway

  • Complete Growth Hormone Insensitivity

  • Gh Receptor Deficiency

  • Primary Gh Insensitivity

  • Short Stature Due To Growth Hormone Resistance

  • LARS

Middle East Respiratory Syndrome
  • Mers

  • Mers - [Middle East Respiratory Syndrome]

Myositis
  • Idiopathic Inflammatory Myopathy

  • Idiopathic Inflammatory Myositis

  • Iim

  • Imm

  • Idiopathic Inflammatory Myopathies

  • Myopathy, Familial Idiopathic Inflammatory

  • Inflammatory Disorder Of Muscle

  • Idiopathic Inflammatory Myopathy, Familial

  • Inflammatory Myopathy, Idiopathic

  • Myopathies Idiopathic Inflammatory

  • Familial Idiopathic Inflammatory Myopathy

Leukemia, Acute Myeloid
  • Acute Myeloid Leukemia

  • Leukemia, Acute Myelogenous

  • Acute Myelogenous Leukemia

  • AML

  • Leukemia, Acute Myeloid, Susceptibility To

  • Acute Myeloblastic Leukemia

  • Leukemia, Acute Myeloid, Reduced Survival In, Somatic

  • Acute Myeloid Leukaemia

  • Leukemia, Myelocytic, Acute

  • Therapy Related Acute Myeloid Leukemia And Myelodysplastic Syndrome

  • Secondary Aml

  • Acute Myelocytic Leukemia

  • Leukemia, Myeloid, Acute

  • Acute Myeloid Leukemia, Somatic

  • Leukemia, Acute Myeloid, Somatic

  • Myeloid Leukemia, Acute, M4/M4eo Subtype, Somatic

  • Acute Myeloblastic Leukaemia

  • Acute Myelogenous Leukaemia

  • Aml - Acute Myeloid Leukemia

  • Acute Myeloid Leukemia With Cebpa Somatic Mutations

  • Aml With Cebpa Somatic Mutations

  • Inherited Acute Myeloid Leukemia

  • Familial Aml

  • Inherited Aml

  • Pure Familial Aml

  • Pure Familial Acute Myeloid Leukemia

  • Secondary Acute Myeloid Leukemia

  • Therapy-Related Aml And Myelodysplastic Syndrome

  • Acute Myeloid Leukemia, Secondary

  • Acute Non-Lymphoblastic Leukemia

  • Acute Non-Lymphocytic Leukemia

  • Acute Biphenotypic Leukemia

  • Acute Undifferentiated Leukemia

  • Acute Myeloblastic Leukaemia With Multilineage Dysplasia

  • Acute Myeloid Leukaemia With Multilineage Dysplasia Without Mention Of Remission

  • Acute Myeloid Leukaemia With Myelodysplasia-Related Features

Lipomatosis
  • Benign Symmetrical Lipomatosis

Lipid Storage Disease
  • Lipoidosis

  • Inborn Lipid Storage Disorder

  • Lipoid Storage Diseas

  • Lipid Storage Diseases

  • Lipidoses

Myocardial Infarction
  • Heart Attack

  • Myocardial Infarction, Susceptibility To

  • Myocardial Infarction 1

  • Myocardial Infarction, Protection Against

  • Myocardial Infarction, Decreased Susceptibility To

  • Myocardial Infarction, Decreased

  • Myocardial Infarct

  • MCI1

  • Premature Myocardial Infarction

  • Myocardial Infarction, Susceptibility To, Type 1

Burkitt Lymphoma
  • Burkitt'S Lymphoma

  • BL

  • Burkitt Lymphoma, Somatic

  • Burkitt Lymphoma/Leukaemia

  • Burkitt'S Tumor

  • Burkitt'S Tumor Or Lymphoma

  • Malignant Lymphoma, Burkitt'S Type

  • Small Non-Cleaved Cell Lymphoma, Burkitt'S Type

  • Small Non-Cleaved Cell Lymphoma

  • Burkitt Tumor

  • Burkitts Lymphoma

  • Lymphoma, Small Noncleaved-Cell

  • Burkitt Tumour

  • Diffuse Small Noncleaved Malignant Burkitt Lymphoma

  • Malignant Burkitt Lymphoma

  • “Burkitt-Like” Lymphoma

  • Undifferentiated Burkitt Lymphoma

  • Small Noncleaved Cell Burkitt Lymphoma

Thrombocytopenia
  • Low Platelet Count

  • Low Platelets

  • Decreased Platelets

  • Platelet Dysfunction Nos

Muscular Dystrophy
  • Muscular Dystrophies

  • Congenital Md

  • Congenital Muscular Dystrophy

  • Cmd

  • Mdc

  • Dystrophy, Muscular

  • Gower'S Muscular Dystrophy

  • Progressive Musclular Dystrophy

  • Pseudohypertrophic Atrophy

  • Pseudohypertrophic Muscle Paralysis

  • Pseudohypertrophic Muscular Atrophy

  • Pseudohypertrophic Muscular Dystrophy

  • Pseudohypertrophic Paralysis

  • Pseudomuscular Hypertrophy

Peripheral Nervous System Disease
  • Peripheral Neuropathy

  • Peripheral Nerve Disease

  • Peripheral Nerve Disorders

  • Neuropathy, Peripheral

  • Peripheral Neuropathy Due To Vitamin Pyridoxine Hyperalimentation

Major Depressive Disorder
  • Seasonal Affective Disorder

  • Unipolar Depression

  • Depression

  • MDD

  • Depressive Disorder

  • Unipolar Depression, Susceptibility To

  • Major Depressive Disorder 1

  • Major Depressive Disorder, Response To Citalopram Therapy In

  • Major Depressive Disorder 2

  • Winter Depression

  • Single Major Depressive Episode

  • Sad

  • Clinical Depression

  • Major Depression

  • Depressive Syndrome

  • Major Depressive Disorder And Accelerated Response To Antidepressant Drug Treatment

  • Seasonal Affective Disorder, Susceptibility To

  • Recurrent Major Depression

  • Affective Disorder, Seasonal

  • Depression In A Seasonal Pattern

  • Depression

  • Seasonal

  • Major Depressive Disorder With A Seasonal Pattern

  • Seasonal Depression

  • Seasonal Mood Disorder

  • Mental Depression

  • Recurrent Major Depressive Episodes

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
Macaca mulatta SIRT1 VGNC VGNC:77233
Mus musculus SIRT1 MGD MGI:2135607
Bos taurus SIRT1 VGNC VGNC:34630
Felis catus SIRT1 VGNC VGNC:65155
Rattus norvegicus SIRT1 RGD RGD:1308542
Canis familiaris SIRT1 VGNC VGNC:46183
Others SIRT1 NCBI