SIRT3 (sirtuin 3) - Rat Genome Database

Send us a Message



Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   
Gene: SIRT3 (sirtuin 3) Homo sapiens
Analyze
Symbol: SIRT3
Name: sirtuin 3
RGD ID: 1318106
HGNC Page HGNC:14931
Description: Enables sequence-specific DNA binding activity and zinc ion binding activity. Involved in aerobic respiration. Located in mitochondrial matrix. Part of protein-containing complex. Biomarker of Alzheimer's disease and type 2 diabetes mellitus.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: hSIRT3; mitochondrial nicotinamide adenine dinucleotide-dependent deacetylase; NAD-dependent deacetylase sirtuin-3, mitochondrial; NAD-dependent protein deacetylase sirtuin-3, mitochondrial; regulatory protein SIR2 homolog 3; silent mating type information regulation 2, S.cerevisiae, homolog 3; sir2-like 3; SIR2-like protein 3; SIR2L3; sirtuin; sirtuin type 3
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh3811215,030 - 236,931 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl11215,030 - 236,931 (-)EnsemblGRCh38hg38GRCh38
GRCh3711215,030 - 236,931 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 3611205,030 - 226,362 (-)NCBINCBI36Build 36hg18NCBI36
Build 3411206,138 - 226,416NCBI
Celera11322,773 - 343,832 (+)NCBICelera
Cytogenetic Map11p15.5NCBI
HuRef1135,047 - 56,030 (-)NCBIHuRef
CHM1_111213,704 - 234,799 (-)NCBICHM1_1
T2T-CHM13v2.011256,228 - 277,937 (-)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
(+)-schisandrin B  (ISO)
(-)-epigallocatechin 3-gallate  (ISO)
(1->4)-beta-D-glucan  (ISO)
(R)-lipoic acid  (ISO)
1,1,1-trichloro-2,2-bis(4-hydroxyphenyl)ethane  (ISO)
1,1-dichloroethene  (ISO)
1,2-dimethylhydrazine  (ISO)
1,3,7,9-tetramethyluric acid  (ISO)
17alpha-ethynylestradiol  (ISO)
17beta-estradiol  (ISO)
2,3,7,8-tetrachlorodibenzodioxine  (EXP,ISO)
2,4-dinitrotoluene  (ISO)
3,5-diethoxycarbonyl-1,4-dihydrocollidine  (ISO)
4-hydroxynon-2-enal  (EXP)
6-chloro-2,3,4,9-tetrahydro-1H-carbazole-1-carboxamide  (EXP,ISO)
6-propyl-2-thiouracil  (ISO)
8-Br-cAMP  (ISO)
ADP  (ISO)
aldehydo-D-glucose  (EXP,ISO)
alpha-mangostin  (EXP,ISO)
amitrole  (ISO)
antimycin A  (EXP)
arsenous acid  (ISO)
ATP  (ISO)
atrazine  (EXP,ISO)
benzo[a]pyrene  (EXP,ISO)
benzo[a]pyrene diol epoxide I  (EXP)
berberine  (EXP)
bisphenol A  (ISO)
Butylbenzyl phthalate  (EXP,ISO)
caffeine  (EXP)
carbon nanotube  (ISO)
CGS-21680  (EXP)
chloroquine  (EXP)
choline  (ISO)
chromium(6+)  (EXP)
cisplatin  (EXP,ISO)
copper(II) sulfate  (EXP)
curcumin  (EXP,ISO)
D-glucose  (EXP,ISO)
deguelin  (EXP)
diarsenic trioxide  (ISO)
diazinon  (EXP)
dibutyl phthalate  (ISO)
diethylstilbestrol  (ISO)
diisononyl phthalate  (EXP)
doxorubicin  (EXP,ISO)
estriol  (ISO)
ethanol  (ISO)
flutamide  (ISO)
folic acid  (ISO)
gentamycin  (ISO)
glucose  (EXP,ISO)
hesperetin  (EXP)
hexadecanoic acid  (EXP)
Honokiol  (ISO)
hydrogen peroxide  (EXP,ISO)
hydrogen sulfide  (EXP,ISO)
hydroquinone  (EXP)
icariin  (ISO)
L-methionine  (ISO)
lead diacetate  (ISO)
linalool  (EXP)
lipoic acid  (ISO)
lipopolysaccharide  (ISO)
mancozeb  (EXP)
maneb  (EXP)
metformin  (EXP,ISO)
methimazole  (ISO)
methotrexate  (ISO)
metiram  (EXP)
mono(2-ethylhexyl) phthalate  (ISO)
N-acetyl-L-cysteine  (EXP,ISO)
N-methyl-4-phenylpyridinium  (ISO)
nebivolol  (ISO)
nicotinamide  (EXP)
paracetamol  (ISO)
paraquat  (ISO)
perfluorooctane-1-sulfonic acid  (EXP,ISO)
perfluorooctanoic acid  (ISO)
pregnenolone 16alpha-carbonitrile  (ISO)
propiconazole  (ISO)
propionic acid  (EXP)
reactive oxygen species  (EXP)
resveratrol  (EXP,ISO)
rotenone  (EXP,ISO)
sodium arsenite  (ISO)
sodium fluoride  (EXP,ISO)
sodium sulfide (anhydrous)  (ISO)
Soman  (ISO)
stavudine  (EXP)
sulfadimethoxine  (ISO)
tenofovir disoproxil fumarate  (EXP)
tert-butyl hydroperoxide  (EXP)
tetrachloromethane  (ISO)
thapsigargin  (EXP)
thioacetamide  (ISO)
trichloroethene  (ISO)
trilobatin  (ISO)
triptonide  (ISO)
tris(2-chloroethyl) phosphate  (EXP)
tunicamycin  (EXP)
urethane  (EXP)
valdecoxib  (ISO)
valproic acid  (EXP)
vancomycin  (ISO)
zidovudine  (EXP)

Molecular Pathway Annotations     Click to see Annotation Detail View
References

References - curated
# Reference Title Reference Citation
1. Maternal obesity during gestation impairs fatty acid oxidation and mitochondrial SIRT3 expression in rat offspring at weaning. Borengasser SJ, etal., PLoS One. 2011;6(8):e24068. doi: 10.1371/journal.pone.0024068. Epub 2011 Aug 25.
2. Sirtuin 3 regulates mouse pancreatic beta cell function and is suppressed in pancreatic islets isolated from human type 2 diabetic patients. Caton PW, etal., Diabetologia. 2013 May;56(5):1068-77. doi: 10.1007/s00125-013-2851-y. Epub 2013 Feb 9.
3. Non-histone lysine acetylated proteins in heart failure. Grillon JM, etal., Biochim Biophys Acta. 2012 Apr;1822(4):607-14. doi: 10.1016/j.bbadis.2011.11.016. Epub 2011 Dec 3.
4. Aerobic interval training protects against myocardial infarction-induced oxidative injury by enhancing antioxidase system and mitochondrial biosynthesis. Jiang HK, etal., Clin Exp Pharmacol Physiol. 2014 Mar;41(3):192-201. doi: 10.1111/1440-1681.12211.
5. Physical and functional HAT/HDAC interplay regulates protein acetylation balance. Peserico A and Simone C, J Biomed Biotechnol. 2011;2011:371832. doi: 10.1155/2011/371832. Epub 2010 Dec 5.
6. Pre-diabetes alters testicular PGC1-alpha/SIRT3 axis modulating mitochondrial bioenergetics and oxidative stress. Rato L, etal., Biochim Biophys Acta. 2014 Mar;1837(3):335-44. doi: 10.1016/j.bbabio.2013.12.008. Epub 2013 Dec 20.
7. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
8. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
9. Lipoic acid improves mitochondrial function in nonalcoholic steatosis through the stimulation of sirtuin 1 and sirtuin 3. Valdecantos MP, etal., Obesity (Silver Spring). 2012 Oct;20(10):1974-83. doi: 10.1038/oby.2012.32. Epub 2012 Feb 13.
10. NAD(+) in aging, metabolism, and neurodegeneration. Verdin E Science. 2015 Dec 4;350(6265):1208-13. doi: 10.1126/science.aac4854.
11. CNS SIRT3 expression is altered by reactive oxygen species and in Alzheimer's disease. Weir HJ, etal., PLoS One. 2012;7(11):e48225. doi: 10.1371/journal.pone.0048225. Epub 2012 Nov 6.
12. Age-Related Decrease in the Mitochondrial Sirtuin Deacetylase Sirt3 Expression Associated with ROS Accumulation in the Auditory Cortex of the Mimetic Aging Rat Model. Zeng L, etal., PLoS One. 2014 Feb 4;9(2):e88019. doi: 10.1371/journal.pone.0088019. eCollection 2014.
Additional References at PubMed
PMID:8889548   PMID:10381378   PMID:10873683   PMID:11056054   PMID:12186850   PMID:12374852   PMID:12477932   PMID:15489334   PMID:15676284   PMID:15719057   PMID:16079181   PMID:16169070  
PMID:16189514   PMID:16788062   PMID:17059877   PMID:17437997   PMID:17456799   PMID:17715127   PMID:17957139   PMID:18215119   PMID:18680753   PMID:18710944   PMID:18781224   PMID:19209188  
PMID:19240061   PMID:19343720   PMID:19367319   PMID:19535340   PMID:19680556   PMID:19714312   PMID:20129246   PMID:20132432   PMID:20198340   PMID:20463968   PMID:20661474   PMID:20800603  
PMID:20819778   PMID:20877624   PMID:20945913   PMID:21358671   PMID:21397863   PMID:21449565   PMID:21460842   PMID:21566644   PMID:21701047   PMID:21840382   PMID:21873635   PMID:22016654  
PMID:22155639   PMID:22309213   PMID:22326535   PMID:22416140   PMID:22585829   PMID:22589271   PMID:22595756   PMID:22609775   PMID:22674009   PMID:22750084   PMID:22770219   PMID:23045395  
PMID:23046812   PMID:23075334   PMID:23272146   PMID:23283301   PMID:23494737   PMID:23665396   PMID:23790338   PMID:23800187   PMID:23839864   PMID:23842789   PMID:23856293   PMID:23868064  
PMID:23898059   PMID:23928404   PMID:23956348   PMID:24026423   PMID:24121500   PMID:24194516   PMID:24252090   PMID:24287180   PMID:24322174   PMID:24324009   PMID:24339251   PMID:24344202  
PMID:24464653   PMID:24486017   PMID:24491532   PMID:24503539   PMID:24746213   PMID:24771001   PMID:24774224   PMID:24877629   PMID:24889606   PMID:24909164   PMID:24924131   PMID:25005846  
PMID:25103363   PMID:25105144   PMID:25109285   PMID:25128872   PMID:25162939   PMID:25165814   PMID:25194924   PMID:25210848   PMID:25221980   PMID:25227106   PMID:25231870   PMID:25284742  
PMID:25329972   PMID:25361925   PMID:25369635   PMID:25562154   PMID:25607838   PMID:25755250   PMID:25755722   PMID:25811481   PMID:25829495   PMID:25915406   PMID:25915842   PMID:25961022  
PMID:26042459   PMID:26045440   PMID:26109058   PMID:26120888   PMID:26121130   PMID:26121691   PMID:26138757   PMID:26141949   PMID:26186194   PMID:26223796   PMID:26225774   PMID:26317998  
PMID:26456643   PMID:26520405   PMID:26577410   PMID:26625292   PMID:26631723   PMID:26667041   PMID:26701732   PMID:26722027   PMID:26743598   PMID:26787646   PMID:26893145   PMID:26950437  
PMID:27034011   PMID:27053302   PMID:27078640   PMID:27114304   PMID:27125970   PMID:27164052   PMID:27216459   PMID:27232755   PMID:27270321   PMID:27277143   PMID:27295248   PMID:27337034  
PMID:27367026   PMID:27420645   PMID:27483432   PMID:27501476   PMID:27604398   PMID:27628218   PMID:27732568   PMID:27773814   PMID:27815257   PMID:27856259   PMID:27881304   PMID:27925196  
PMID:28032248   PMID:28108513   PMID:28161643   PMID:28196907   PMID:28197634   PMID:28213977   PMID:28239025   PMID:28248093   PMID:28258190   PMID:28347248   PMID:28368421   PMID:28380382  
PMID:28429188   PMID:28459202   PMID:28514442   PMID:28526626   PMID:28536275   PMID:28567457   PMID:28711502   PMID:28717408   PMID:28737710   PMID:28760703   PMID:28867266   PMID:28878358  
PMID:28947845   PMID:29072685   PMID:29103158   PMID:29130578   PMID:29136592   PMID:29220206   PMID:29243781   PMID:29277324   PMID:29323702   PMID:29330215   PMID:29411439   PMID:29421536  
PMID:29445193   PMID:29466723   PMID:29509190   PMID:29567426   PMID:29568061   PMID:29574628   PMID:29683756   PMID:29898623   PMID:29915029   PMID:30021354   PMID:30091830   PMID:30095923  
PMID:30107294   PMID:30126181   PMID:30132870   PMID:30216853   PMID:30250024   PMID:30367038   PMID:30412732   PMID:30487699   PMID:30572719   PMID:30641770   PMID:30683653   PMID:30691320  
PMID:30736780   PMID:30774023   PMID:30829051   PMID:30958373   PMID:30993888   PMID:31037127   PMID:31055111   PMID:31108370   PMID:31153640   PMID:31185214   PMID:31188638   PMID:31189433  
PMID:31201798   PMID:31292999   PMID:31677030   PMID:31723239   PMID:31740222   PMID:31812668   PMID:31894331   PMID:31930676   PMID:31991048   PMID:32195489   PMID:32229158   PMID:32305451  
PMID:32329068   PMID:32403131   PMID:32428596   PMID:32462533   PMID:32495859   PMID:32507768   PMID:32681437   PMID:32703935   PMID:32724473   PMID:32747616   PMID:32814053   PMID:32951306  
PMID:33003340   PMID:33115805   PMID:33143333   PMID:33147367   PMID:33160987   PMID:33184465   PMID:33231084   PMID:33241954   PMID:33273545   PMID:33282964   PMID:33393034   PMID:33423553  
PMID:33461161   PMID:33530998   PMID:33565085   PMID:33610576   PMID:33624391   PMID:33655712   PMID:33662874   PMID:33669567   PMID:33706382   PMID:33845483   PMID:33857259   PMID:33861984  
PMID:33872694   PMID:33945069   PMID:33961781   PMID:34001853   PMID:34079125   PMID:34148409   PMID:34232204   PMID:34244482   PMID:34271087   PMID:34278469   PMID:34338986   PMID:34363948  
PMID:34396428   PMID:34446002   PMID:34500051   PMID:34514931   PMID:34518519   PMID:34630854   PMID:34664305   PMID:34686511   PMID:34747319   PMID:34747550   PMID:34758305   PMID:34768083  
PMID:35086984   PMID:35104011   PMID:35150983   PMID:35195783   PMID:35418250   PMID:35580464   PMID:35594990   PMID:35729330   PMID:35791925   PMID:35832490   PMID:35976439   PMID:35980861  
PMID:36010644   PMID:36012382   PMID:36083252   PMID:36134579   PMID:36215168   PMID:36374406   PMID:36437337   PMID:36594098   PMID:36596388   PMID:36598711   PMID:36657406   PMID:36675125  
PMID:36688989   PMID:36692509   PMID:36708431   PMID:36739437   PMID:36740765   PMID:36871142   PMID:36871899   PMID:36974538   PMID:36991356   PMID:37028501   PMID:37073806   PMID:37163276  
PMID:37196680   PMID:37238605   PMID:37343939   PMID:37392543   PMID:37481555   PMID:37537789   PMID:37651673   PMID:37789393   PMID:37996927   PMID:38233193   PMID:38242748   PMID:38255792  
PMID:38261767   PMID:38285890   PMID:38395990  


Genomics

Comparative Map Data
SIRT3
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh3811215,030 - 236,931 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl11215,030 - 236,931 (-)EnsemblGRCh38hg38GRCh38
GRCh3711215,030 - 236,931 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 3611205,030 - 226,362 (-)NCBINCBI36Build 36hg18NCBI36
Build 3411206,138 - 226,416NCBI
Celera11322,773 - 343,832 (+)NCBICelera
Cytogenetic Map11p15.5NCBI
HuRef1135,047 - 56,030 (-)NCBIHuRef
CHM1_111213,704 - 234,799 (-)NCBICHM1_1
T2T-CHM13v2.011256,228 - 277,937 (-)NCBIT2T-CHM13v2.0
Sirt3
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm397140,443,576 - 140,462,222 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl7140,443,579 - 140,462,222 (-)EnsemblGRCm39 Ensembl
GRCm387140,863,663 - 140,882,309 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl7140,863,666 - 140,882,309 (-)EnsemblGRCm38mm10GRCm38
MGSCv377148,049,562 - 148,068,208 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv367140,714,990 - 140,733,629 (-)NCBIMGSCv36mm8
Celera7140,655,950 - 140,674,596 (-)NCBICelera
Cytogenetic Map7F4- F5NCBI
cM Map786.07NCBI
Sirt3
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81205,371,703 - 205,394,145 (-)NCBIGRCr8
mRatBN7.21195,942,066 - 195,964,472 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1195,942,073 - 195,964,808 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx1204,294,536 - 204,318,293 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01211,421,447 - 211,445,196 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.01204,095,300 - 204,119,047 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.01213,613,502 - 213,636,061 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1213,613,513 - 213,635,546 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01220,539,132 - 220,561,380 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41201,021,391 - 201,043,756 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.11201,172,601 - 201,193,816 (-)NCBI
Celera1193,586,014 - 193,607,810 (-)NCBICelera
Cytogenetic Map1q41NCBI
Sirt3
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495547611,794,951 - 11,826,237 (+)EnsemblChiLan1.0
ChiLan1.0NW_00495547611,794,951 - 11,826,244 (+)NCBIChiLan1.0ChiLan1.0
SIRT3
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v292,582,959 - 2,605,626 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan1111,737,925 - 1,761,366 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v011210,052 - 233,969 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.111255,191 - 863,031 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl11255,191 - 278,732 (-)Ensemblpanpan1.1panPan2
SIRT3
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.11825,369,183 - 25,388,126 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl1825,369,382 - 25,388,118 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha1825,019,130 - 25,038,115 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.01825,895,720 - 25,914,839 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl1825,895,722 - 25,914,795 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.11825,463,734 - 25,482,834 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.01825,108,512 - 25,127,612 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.01825,721,366 - 25,740,351 (-)NCBIUU_Cfam_GSD_1.0
Sirt3
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440494763,131 - 78,513 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_00493688863,546 - 77,950 (-)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_00493688863,131 - 78,536 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
SIRT3
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl238,464 - 55,101 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1238,465 - 55,074 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.22162,169,820 - 162,186,214 (+)NCBISscrofa10.2Sscrofa10.2susScr3
SIRT3
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1125,740 - 49,471 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl126,927 - 48,944 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366603897,040,657 - 97,063,458 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Sirt3
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_00462476622,199,601 - 22,233,933 (+)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_00462476622,199,741 - 22,233,933 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in SIRT3
32 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 11p15.5(chr11:196966-244236)x1 copy number loss Abnormal facial shape [RCV000050265]|See cases [RCV000050265] Chr11:196966..244236 [GRCh38]
Chr11:196966..244236 [GRCh37]
Chr11:11p15.5
uncertain significance
GRCh38/hg38 11p15.5-15.4(chr11:196966-3377077)x3 copy number gain See cases [RCV000050947] Chr11:196966..3377077 [GRCh38]
Chr11:196966..3398307 [GRCh37]
Chr11:186966..3354883 [NCBI36]
Chr11:11p15.5-15.4
pathogenic
GRCh38/hg38 11p15.5-15.4(chr11:196966-4435344)x3 copy number gain See cases [RCV000050927] Chr11:196966..4435344 [GRCh38]
Chr11:196966..4456574 [GRCh37]
Chr11:186966..4413150 [NCBI36]
Chr11:11p15.5-15.4
pathogenic
GRCh38/hg38 11p15.5(chr11:196966-251588)x3 copy number gain See cases [RCV000051693] Chr11:196966..251588 [GRCh38]
Chr11:196966..251588 [GRCh37]
Chr11:186966..241588 [NCBI36]
Chr11:11p15.5
uncertain significance
GRCh38/hg38 11p15.5-15.4(chr11:218365-3377077)x3 copy number gain See cases [RCV000053614] Chr11:218365..3377077 [GRCh38]
Chr11:218365..3398307 [GRCh37]
Chr11:208365..3354883 [NCBI36]
Chr11:11p15.5-15.4
pathogenic
GRCh38/hg38 11p15.5-15.4(chr11:196966-3624139)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053592]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053592]|See cases [RCV000053592] Chr11:196966..3624139 [GRCh38]
Chr11:196966..3645369 [GRCh37]
Chr11:186966..3601945 [NCBI36]
Chr11:11p15.5-15.4
pathogenic
GRCh38/hg38 11p15.5-13(chr11:202758-31726224)x3 copy number gain See cases [RCV000053613] Chr11:202758..31726224 [GRCh38]
Chr11:202758..31747772 [GRCh37]
Chr11:192758..31704348 [NCBI36]
Chr11:11p15.5-13
pathogenic
NM_012239.5(SIRT3):c.414G>A (p.Gln138=) single nucleotide variant Malignant melanoma [RCV000069299] Chr11:233402 [GRCh38]
Chr11:233402 [GRCh37]
Chr11:223402 [NCBI36]
Chr11:11p15.5
not provided
GRCh37/hg19 11p15.5-15.4(chr11:10701-5080415)x2 copy number gain See cases [RCV001310286] Chr11:10701..5080415 [GRCh37]
Chr11:11p15.5-15.4
pathogenic
GRCh38/hg38 11p15.5(chr11:196966-244236)x1 copy number loss See cases [RCV000050265] Chr11:196966..244236 [GRCh38]
Chr11:196966..244236 [GRCh37]
Chr11:186966..234236 [NCBI36]
Chr11:11p15.5
uncertain significance
GRCh38/hg38 11p15.5(chr11:196966-244236)x3 copy number gain See cases [RCV000133626] Chr11:196966..244236 [GRCh38]
Chr11:196966..244236 [GRCh37]
Chr11:186966..234236 [NCBI36]
Chr11:11p15.5
benign
GRCh38/hg38 11p15.5-15.4(chr11:61793-10727969)x3 copy number gain See cases [RCV000139987] Chr11:61793..10727969 [GRCh38]
Chr11:61793..10749516 [GRCh37]
Chr11:51793..10706092 [NCBI36]
Chr11:11p15.5-15.4
pathogenic
GRCh38/hg38 11p15.5(chr11:200222-237805)x3 copy number gain See cases [RCV000140063] Chr11:200222..237805 [GRCh38]
Chr11:200222..237805 [GRCh37]
Chr11:190222..227805 [NCBI36]
Chr11:11p15.5
benign
GRCh38/hg38 11p15.5-15.4(chr11:196855-5321874)x3 copy number gain See cases [RCV000142890] Chr11:196855..5321874 [GRCh38]
Chr11:196855..5343104 [GRCh37]
Chr11:186855..5299680 [NCBI36]
Chr11:11p15.5-15.4
pathogenic
GRCh38/hg38 11p15.5(chr11:196855-2116185)x3 copy number gain See cases [RCV000142923] Chr11:196855..2116185 [GRCh38]
Chr11:196855..2137415 [GRCh37]
Chr11:186855..2093991 [NCBI36]
Chr11:11p15.5
pathogenic
GRCh37/hg19 11p15.5(chr11:193142-299384)x3 copy number gain See cases [RCV000240198] Chr11:193142..299384 [GRCh37]
Chr11:11p15.5
uncertain significance
GRCh37/hg19 11p15.5-15.4(chr11:193187-5291338)x3 copy number gain See cases [RCV000446036] Chr11:193187..5291338 [GRCh37]
Chr11:11p15.5-15.4
pathogenic
GRCh37/hg19 11p15.5(chr11:210300-487062)x3 copy number gain not provided [RCV000762783] Chr11:210300..487062 [GRCh37]
Chr11:11p15.5
uncertain significance
GRCh37/hg19 11p15.5(chr11:193842-475940)x3 copy number gain See cases [RCV000449391] Chr11:193842..475940 [GRCh37]
Chr11:11p15.5
likely benign
GRCh37/hg19 11p15.5-15.4(chr11:230615-6644927)x3 copy number gain See cases [RCV000449417] Chr11:230615..6644927 [GRCh37]
Chr11:11p15.5-15.4
pathogenic
GRCh37/hg19 11p15.5(chr11:230615-378405)x1 copy number loss See cases [RCV000510242] Chr11:230615..378405 [GRCh37]
Chr11:11p15.5
uncertain significance
GRCh37/hg19 11p15.5-q25(chr11:230616-134938470) copy number gain See cases [RCV000511729] Chr11:230616..134938470 [GRCh37]
Chr11:11p15.5-q25
pathogenic
GRCh37/hg19 11p15.5-12(chr11:230615-37698540)x3 copy number gain See cases [RCV000511561] Chr11:230615..37698540 [GRCh37]
Chr11:11p15.5-12
pathogenic
GRCh37/hg19 11p15.5(chr11:230615-253390)x1 copy number loss See cases [RCV000511701] Chr11:230615..253390 [GRCh37]
Chr11:11p15.5
uncertain significance
GRCh37/hg19 11p15.5-q25(chr11:230616-134938470)x3 copy number gain See cases [RCV000510881] Chr11:230616..134938470 [GRCh37]
Chr11:11p15.5-q25
pathogenic
NM_012239.6(SIRT3):c.1108G>A (p.Val370Met) single nucleotide variant Inborn genetic diseases [RCV003284626] Chr11:218903 [GRCh38]
Chr11:218903 [GRCh37]
Chr11:11p15.5
uncertain significance
NM_012239.6(SIRT3):c.946C>T (p.Leu316Phe) single nucleotide variant Inborn genetic diseases [RCV003241774] Chr11:224101 [GRCh38]
Chr11:224101 [GRCh37]
Chr11:11p15.5
uncertain significance
GRCh37/hg19 11p15.5-14.3(chr11:230615-25584362)x3 copy number gain See cases [RCV000512225] Chr11:230615..25584362 [GRCh37]
Chr11:11p15.5-14.3
pathogenic
GRCh37/hg19 11p15.5-13(chr11:230615-31995219)x3 copy number gain See cases [RCV000512477] Chr11:230615..31995219 [GRCh37]
Chr11:11p15.5-13
pathogenic
GRCh37/hg19 11p15.5-15.1(chr11:230615-17099213)x3 copy number gain not provided [RCV000683372] Chr11:230615..17099213 [GRCh37]
Chr11:11p15.5-15.1
pathogenic
GRCh37/hg19 11p15.5-15.4(chr11:230615-9704511)x3 copy number gain not provided [RCV000683369] Chr11:230615..9704511 [GRCh37]
Chr11:11p15.5-15.4
pathogenic
GRCh37/hg19 11p15.5-q25(chr11:198510-134934063)x3 copy number gain not provided [RCV000737348] Chr11:198510..134934063 [GRCh37]
Chr11:11p15.5-q25
pathogenic
GRCh37/hg19 11p15.5-q25(chr11:70864-134938470)x3 copy number gain not provided [RCV000749874] Chr11:70864..134938470 [GRCh37]
Chr11:11p15.5-q25
pathogenic
GRCh37/hg19 11p15.5(chr11:122751-257030)x3 copy number gain not provided [RCV000737344] Chr11:122751..257030 [GRCh37]
Chr11:11p15.5
benign
GRCh37/hg19 11p15.5(chr11:198510-247972)x3 copy number gain not provided [RCV000737346] Chr11:198510..247972 [GRCh37]
Chr11:11p15.5
benign
GRCh37/hg19 11p15.5(chr11:198510-396308)x3 copy number gain not provided [RCV000737347] Chr11:198510..396308 [GRCh37]
Chr11:11p15.5
benign
GRCh37/hg19 11p15.5-15.3(chr11:193146-12643136) copy number gain Silver-Russell syndrome 1 [RCV000767567] Chr11:193146..12643136 [GRCh37]
Chr11:11p15.5-15.3
pathogenic
NM_012239.6(SIRT3):c.785C>A (p.Pro262His) single nucleotide variant not provided [RCV000963938] Chr11:230474 [GRCh38]
Chr11:230474 [GRCh37]
Chr11:11p15.5
benign
GRCh37/hg19 11p15.5(chr11:210898-461373)x3 copy number gain not provided [RCV000849684] Chr11:210898..461373 [GRCh37]
Chr11:11p15.5
uncertain significance
GRCh37/hg19 11p15.5(chr11:230615-253390)x1 copy number loss not provided [RCV000846299] Chr11:230615..253390 [GRCh37]
Chr11:11p15.5
uncertain significance
NM_012239.6(SIRT3):c.242G>A (p.Arg81Lys) single nucleotide variant Inborn genetic diseases [RCV003240391] Chr11:236087 [GRCh38]
Chr11:236087 [GRCh37]
Chr11:11p15.5
uncertain significance
NM_012239.6(SIRT3):c.488G>A (p.Gly163Asp) single nucleotide variant Inborn genetic diseases [RCV003252687] Chr11:233201 [GRCh38]
Chr11:233201 [GRCh37]
Chr11:11p15.5
uncertain significance
NM_012239.6(SIRT3):c.235T>C (p.Phe79Leu) single nucleotide variant SIRT3-related condition [RCV003930498]|not provided [RCV000880116] Chr11:236094 [GRCh38]
Chr11:236094 [GRCh37]
Chr11:11p15.5
benign|likely benign
GRCh37/hg19 11p15.5-13(chr11:235934-33826995)x3 copy number gain not provided [RCV001006372] Chr11:235934..33826995 [GRCh37]
Chr11:11p15.5-13
pathogenic
GRCh37/hg19 11p15.5-15.4(chr11:230615-4851537)x3 copy number gain See cases [RCV001263059] Chr11:230615..4851537 [GRCh37]
Chr11:11p15.5-15.4
pathogenic
GRCh37/hg19 11p15.5(chr11:230615-1150353)x3 copy number gain not provided [RCV001259592] Chr11:230615..1150353 [GRCh37]
Chr11:11p15.5
uncertain significance
GRCh37/hg19 11p15.5-15.4(chr11:210300-8664358)x3 copy number gain Silver-Russell syndrome 1 [RCV001263222] Chr11:210300..8664358 [GRCh37]
Chr11:11p15.5-15.4
pathogenic
GRCh37/hg19 11p15.5-15.4(chr11:230615-5525355)x3 copy number gain not provided [RCV001825269] Chr11:230615..5525355 [GRCh37]
Chr11:11p15.5-15.4
not provided
NC_000011.9:g.(?_216698)_(720766_?)dup duplication Immunodeficiency 39 [RCV001923869] Chr11:216698..720766 [GRCh37]
Chr11:11p15.5
uncertain significance
NC_000011.9:g.(?_216698)_(299504_?)dup duplication not provided [RCV001916212] Chr11:216698..299504 [GRCh37]
Chr11:11p15.5
uncertain significance
GRCh37/hg19 11p15.5-14.2(chr11:230615-26881146)x3 copy number gain See cases [RCV002286351] Chr11:230615..26881146 [GRCh37]
Chr11:11p15.5-14.2
pathogenic
GRCh37/hg19 11p15.5-15.4(chr11:230616-8250724)x3 copy number gain not provided [RCV002472435] Chr11:230616..8250724 [GRCh37]
Chr11:11p15.5-15.4
pathogenic
NM_012239.6(SIRT3):c.197C>G (p.Pro66Arg) single nucleotide variant Inborn genetic diseases [RCV002981522] Chr11:236132 [GRCh38]
Chr11:236132 [GRCh37]
Chr11:11p15.5
uncertain significance
NM_012239.6(SIRT3):c.994G>A (p.Glu332Lys) single nucleotide variant Inborn genetic diseases [RCV002980135] Chr11:219017 [GRCh38]
Chr11:219017 [GRCh37]
Chr11:11p15.5
uncertain significance
NM_012239.6(SIRT3):c.710C>T (p.Ser237Leu) single nucleotide variant Inborn genetic diseases [RCV002888998] Chr11:230549 [GRCh38]
Chr11:230549 [GRCh37]
Chr11:11p15.5
uncertain significance
NM_012239.6(SIRT3):c.320G>T (p.Gly107Val) single nucleotide variant Inborn genetic diseases [RCV002798345] Chr11:233496 [GRCh38]
Chr11:233496 [GRCh37]
Chr11:11p15.5
uncertain significance
NM_012239.6(SIRT3):c.452C>G (p.Pro151Arg) single nucleotide variant Inborn genetic diseases [RCV002660237] Chr11:233364 [GRCh38]
Chr11:233364 [GRCh37]
Chr11:11p15.5
uncertain significance
NM_012239.6(SIRT3):c.479C>A (p.Pro160Gln) single nucleotide variant Inborn genetic diseases [RCV002951842] Chr11:233210 [GRCh38]
Chr11:233210 [GRCh37]
Chr11:11p15.5
uncertain significance
NM_012239.6(SIRT3):c.665T>C (p.Leu222Pro) single nucleotide variant Inborn genetic diseases [RCV002704212] Chr11:233024 [GRCh38]
Chr11:233024 [GRCh37]
Chr11:11p15.5
uncertain significance
NM_012239.6(SIRT3):c.868G>A (p.Asp290Asn) single nucleotide variant Inborn genetic diseases [RCV002984732] Chr11:224179 [GRCh38]
Chr11:224179 [GRCh37]
Chr11:11p15.5
uncertain significance
NM_012239.6(SIRT3):c.1154A>T (p.Asp385Val) single nucleotide variant Inborn genetic diseases [RCV002748071] Chr11:218857 [GRCh38]
Chr11:218857 [GRCh37]
Chr11:11p15.5
uncertain significance
NM_012239.6(SIRT3):c.806G>A (p.Arg269Gln) single nucleotide variant Inborn genetic diseases [RCV002657187] Chr11:230453 [GRCh38]
Chr11:230453 [GRCh37]
Chr11:11p15.5
uncertain significance
NM_012239.6(SIRT3):c.146G>T (p.Gly49Val) single nucleotide variant Inborn genetic diseases [RCV003256163] Chr11:236183 [GRCh38]
Chr11:236183 [GRCh37]
Chr11:11p15.5
uncertain significance
NM_012239.6(SIRT3):c.159C>A (p.Ser53Arg) single nucleotide variant Inborn genetic diseases [RCV003211348] Chr11:236170 [GRCh38]
Chr11:236170 [GRCh37]
Chr11:11p15.5
uncertain significance
NM_012239.6(SIRT3):c.691G>A (p.Asp231Asn) single nucleotide variant Inborn genetic diseases [RCV003209110] Chr11:232998 [GRCh38]
Chr11:232998 [GRCh37]
Chr11:11p15.5
uncertain significance
NM_012239.6(SIRT3):c.422T>C (p.Val141Ala) single nucleotide variant Inborn genetic diseases [RCV003185347] Chr11:233394 [GRCh38]
Chr11:233394 [GRCh37]
Chr11:11p15.5
uncertain significance
NM_012239.6(SIRT3):c.828G>C (p.Arg276Ser) single nucleotide variant Inborn genetic diseases [RCV003345982] Chr11:224219 [GRCh38]
Chr11:224219 [GRCh37]
Chr11:11p15.5
uncertain significance
GRCh37/hg19 11p15.5-15.4(chr11:192764-3362853)x3 copy number gain not provided [RCV003484828] Chr11:192764..3362853 [GRCh37]
Chr11:11p15.5-15.4
pathogenic
GRCh37/hg19 11p15.5-15.4(chr11:230615-8821443)x3 copy number gain Russell-Silver syndrome [RCV003444025] Chr11:230615..8821443 [GRCh37]
Chr11:11p15.5-15.4
pathogenic
NM_012239.6(SIRT3):c.33C>T (p.Ala11=) single nucleotide variant SIRT3-related condition [RCV003904060] Chr11:236296 [GRCh38]
Chr11:236296 [GRCh37]
Chr11:11p15.5
likely benign
NM_012239.6(SIRT3):c.477G>T (p.Ser159=) single nucleotide variant SIRT3-related condition [RCV003984600] Chr11:233212 [GRCh38]
Chr11:233212 [GRCh37]
Chr11:11p15.5
benign
NM_012239.6(SIRT3):c.238C>T (p.Arg80Trp) single nucleotide variant SIRT3-related condition [RCV003973953] Chr11:236091 [GRCh38]
Chr11:236091 [GRCh37]
Chr11:11p15.5
benign
NM_012239.6(SIRT3):c.1104C>T (p.His368=) single nucleotide variant SIRT3-related condition [RCV003964328] Chr11:218907 [GRCh38]
Chr11:218907 [GRCh37]
Chr11:11p15.5
benign
NM_012239.6(SIRT3):c.843G>A (p.Pro281=) single nucleotide variant SIRT3-related condition [RCV003907000] Chr11:224204 [GRCh38]
Chr11:224204 [GRCh37]
Chr11:11p15.5
benign
NM_012239.6(SIRT3):c.483G>T (p.Gly161=) single nucleotide variant SIRT3-related condition [RCV003904597] Chr11:233206 [GRCh38]
Chr11:233206 [GRCh37]
Chr11:11p15.5
likely benign
NM_012239.6(SIRT3):c.622G>A (p.Val208Ile) single nucleotide variant SIRT3-related condition [RCV003982290] Chr11:233067 [GRCh38]
Chr11:233067 [GRCh37]
Chr11:11p15.5
benign
NM_012239.6(SIRT3):c.-9G>C single nucleotide variant SIRT3-related condition [RCV003919801] Chr11:236337 [GRCh38]
Chr11:236337 [GRCh37]
Chr11:11p15.5
benign
NM_012239.6(SIRT3):c.853G>A (p.Gly285Ser) single nucleotide variant SIRT3-related condition [RCV003941991] Chr11:224194 [GRCh38]
Chr11:224194 [GRCh37]
Chr11:11p15.5
likely benign
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:5028
Count of miRNA genes:1104
Interacting mature miRNAs:1408
Transcripts:ENST00000382743, ENST00000524564, ENST00000525237, ENST00000525319, ENST00000525776, ENST00000526854, ENST00000528469, ENST00000528702, ENST00000529055, ENST00000529382, ENST00000529937, ENST00000530067, ENST00000531753, ENST00000532837, ENST00000532956, ENST00000534381
Prediction methods:Microtar, Miranda, Rnahybrid
Result types:miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.

Markers in Region
D11S3074  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3711223,322 - 223,438UniSTSGRCh37
Build 3611213,322 - 213,438RGDNCBI36
Celera11335,575 - 335,691RGD
Cytogenetic Map11p15.5UniSTS
HuRef1143,188 - 43,304UniSTS
RH78086  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3711216,267 - 216,417UniSTSGRCh37
Build 3611206,267 - 206,417RGDNCBI36
Celera11342,445 - 342,595RGD
Cytogenetic Map11p15.5UniSTS
HuRef1136,284 - 36,434UniSTS
GeneMap99-GB4 RH Map1118.88UniSTS
SIRT3_3197.2  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3711215,978 - 216,682UniSTSGRCh37
Build 3611205,978 - 206,682RGDNCBI36
Celera11342,180 - 342,884RGD
HuRef1135,995 - 36,699UniSTS
RH15952  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3711215,582 - 215,704UniSTSGRCh37
Build 3611205,582 - 205,704RGDNCBI36
Celera11343,158 - 343,280RGD
Cytogenetic Map11p15.5UniSTS
HuRef1135,599 - 35,721UniSTS
GeneMap99-GB4 RH Map1122.62UniSTS
NCBI RH Map1110.0UniSTS
WI-19967  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3711214,753 - 215,023UniSTSGRCh37
Build 3611204,753 - 205,023RGDNCBI36
Celera11343,839 - 344,109RGD
Cytogenetic Map11p15.5UniSTS
HuRef1134,770 - 35,040UniSTS
GeneMap99-GB4 RH Map1122.82UniSTS
Whitehead-RH Map1115.6UniSTS
NCBI RH Map1110.0UniSTS
A004P12  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3711215,430 - 215,558UniSTSGRCh37
Build 3611205,430 - 205,558RGDNCBI36
Celera11343,304 - 343,432RGD
Cytogenetic Map11p15.5UniSTS
HuRef1135,447 - 35,575UniSTS
GeneMap99-GB4 RH Map1122.62UniSTS
NCBI RH Map1110.0UniSTS
G19667  
Human AssemblyChrPosition (strand)SourceJBrowse
Celera11343,852 - 343,973RGD
Cytogenetic Map11p15.5UniSTS
A001U35  
Human AssemblyChrPosition (strand)SourceJBrowse
Celera11343,852 - 343,973RGD
Cytogenetic Map11p15.5UniSTS
GeneMap99-GB4 RH Map1120.7UniSTS
NCBI RH Map1110.0UniSTS


Expression


RNA-SEQ Expression
High: > 1000 TPM value   Medium: Between 11 and 1000 TPM
Low: Between 0.5 and 10 TPM   Below Cutoff: < 0.5 TPM

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system visual system adipose tissue appendage entire extraembryonic component pharyngeal arch
High
Medium 1297 1276 1410 322 877 240 2872 997 2942 278 1284 1260 91 657 1852 1
Low 1142 1709 316 302 1068 225 1485 1200 792 141 176 353 84 1 547 936 6 1
Below cutoff 6 6

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001017524 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001370310 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001370312 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001370314 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001370315 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001370316 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001370317 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001370318 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001370319 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001370320 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001370321 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001370322 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001370323 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001370324 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001370325 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_012239 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_163386 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_163387 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_163388 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_163389 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_163390 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_163391 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_163392 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_163393 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_163394 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_163395 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_163396 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_163397 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_163398 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_163399 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_163400 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_163401 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_163402 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011519956 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011519957 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017017431 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024448410 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047426677 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054368236 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054368237 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054368238 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054368239 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_007062467 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_008488374 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AA279020 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC069287 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC136475 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF015416 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF083108 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AI091200 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK074992 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK298572 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK299009 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK299438 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK301558 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK301979 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK308681 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK316175 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL137276 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL535769 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC001042 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BI755839 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BM709066 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BM973763 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471278 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068267 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CS330056 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CS330058 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CS417199 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CS545590 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DR762907 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HY006161 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  U73637 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

RefSeq Acc Id: ENST00000382743   ⟹   ENSP00000372191
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl11215,030 - 236,342 (-)Ensembl
RefSeq Acc Id: ENST00000524564   ⟹   ENSP00000432937
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl11216,391 - 236,354 (-)Ensembl
RefSeq Acc Id: ENST00000525237   ⟹   ENSP00000436085
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl11233,209 - 236,326 (-)Ensembl
RefSeq Acc Id: ENST00000525319   ⟹   ENSP00000435464
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl11216,206 - 236,354 (-)Ensembl
RefSeq Acc Id: ENST00000525776   ⟹   ENSP00000433132
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl11233,192 - 233,683 (-)Ensembl
RefSeq Acc Id: ENST00000526854   ⟹   ENSP00000435505
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl11224,167 - 236,330 (-)Ensembl
RefSeq Acc Id: ENST00000528469   ⟹   ENSP00000432857
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl11232,983 - 236,859 (-)Ensembl
RefSeq Acc Id: ENST00000528702
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl11225,673 - 236,931 (-)Ensembl
RefSeq Acc Id: ENST00000529055   ⟹   ENSP00000437179
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl11224,222 - 236,339 (-)Ensembl
RefSeq Acc Id: ENST00000529382   ⟹   ENSP00000437216
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl11216,611 - 236,834 (-)Ensembl
RefSeq Acc Id: ENST00000529937   ⟹   ENSP00000434747
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl11216,145 - 236,337 (-)Ensembl
RefSeq Acc Id: ENST00000530067   ⟹   ENSP00000435014
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl11230,603 - 236,345 (-)Ensembl
RefSeq Acc Id: ENST00000531753
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl11224,090 - 233,928 (-)Ensembl
RefSeq Acc Id: ENST00000532837   ⟹   ENSP00000433899
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl11216,179 - 236,343 (-)Ensembl
RefSeq Acc Id: ENST00000532956   ⟹   ENSP00000433077
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl11216,525 - 236,352 (-)Ensembl
RefSeq Acc Id: ENST00000534381
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl11225,762 - 230,692 (-)Ensembl
RefSeq Acc Id: NM_001017524   ⟹   NP_001017524
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3811215,030 - 236,342 (-)NCBI
GRCh3711215,030 - 236,362 (-)ENTREZGENE
GRCh3711215,030 - 236,362 (-)NCBI
Build 3611205,030 - 226,362 (-)NCBI Archive
HuRef1135,047 - 56,030 (-)ENTREZGENE
CHM1_111213,704 - 234,799 (-)NCBI
T2T-CHM13v2.011256,228 - 277,334 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001370310   ⟹   NP_001357239
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3811215,030 - 236,342 (-)NCBI
T2T-CHM13v2.011256,228 - 277,334 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001370312   ⟹   NP_001357241
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3811215,030 - 236,342 (-)NCBI
T2T-CHM13v2.011256,228 - 277,334 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001370314   ⟹   NP_001357243
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3811215,030 - 236,342 (-)NCBI
T2T-CHM13v2.011256,228 - 277,334 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001370315   ⟹   NP_001357244
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3811215,030 - 236,342 (-)NCBI
T2T-CHM13v2.011256,228 - 277,334 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001370316   ⟹   NP_001357245
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3811215,030 - 236,342 (-)NCBI
T2T-CHM13v2.011256,228 - 277,334 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001370317   ⟹   NP_001357246
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3811215,030 - 236,931 (-)NCBI
T2T-CHM13v2.011256,228 - 277,937 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001370318   ⟹   NP_001357247
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3811215,030 - 236,931 (-)NCBI
T2T-CHM13v2.011256,228 - 277,937 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001370319   ⟹   NP_001357248
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3811215,030 - 236,931 (-)NCBI
T2T-CHM13v2.011256,228 - 277,937 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001370320   ⟹   NP_001357249
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3811215,030 - 236,931 (-)NCBI
T2T-CHM13v2.011256,228 - 277,937 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001370321   ⟹   NP_001357250
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3811215,030 - 236,931 (-)NCBI
T2T-CHM13v2.011256,228 - 277,937 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001370322   ⟹   NP_001357251
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3811215,030 - 236,931 (-)NCBI
T2T-CHM13v2.011256,228 - 277,937 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001370323   ⟹   NP_001357252
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3811215,030 - 236,342 (-)NCBI
T2T-CHM13v2.011256,228 - 277,334 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001370324   ⟹   NP_001357253
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3811215,030 - 236,931 (-)NCBI
T2T-CHM13v2.011256,228 - 277,937 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001370325   ⟹   NP_001357254
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3811215,030 - 236,342 (-)NCBI
T2T-CHM13v2.011256,228 - 277,334 (-)NCBI
Sequence:
RefSeq Acc Id: NM_012239   ⟹   NP_036371
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3811215,030 - 236,342 (-)NCBI
GRCh3711215,030 - 236,362 (-)ENTREZGENE
GRCh3711215,030 - 236,362 (-)NCBI
Build 3611205,030 - 226,362 (-)NCBI Archive
HuRef1135,047 - 56,030 (-)ENTREZGENE
CHM1_111213,704 - 234,799 (-)NCBI
T2T-CHM13v2.011256,228 - 277,334 (-)NCBI
Sequence:
RefSeq Acc Id: NR_163386
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3811215,030 - 236,931 (-)NCBI
T2T-CHM13v2.011256,228 - 277,937 (-)NCBI
Sequence:
RefSeq Acc Id: NR_163387
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3811215,030 - 236,931 (-)NCBI
T2T-CHM13v2.011256,228 - 277,937 (-)NCBI
Sequence:
RefSeq Acc Id: NR_163388
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3811215,030 - 236,931 (-)NCBI
T2T-CHM13v2.011256,228 - 277,937 (-)NCBI
Sequence:
RefSeq Acc Id: NR_163389
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3811215,030 - 236,931 (-)NCBI
T2T-CHM13v2.011256,228 - 277,937 (-)NCBI
Sequence:
RefSeq Acc Id: NR_163390
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3811215,030 - 236,931 (-)NCBI
T2T-CHM13v2.011256,228 - 277,937 (-)NCBI
Sequence:
RefSeq Acc Id: NR_163391
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3811215,030 - 236,931 (-)NCBI
T2T-CHM13v2.011256,228 - 277,937 (-)NCBI
Sequence:
RefSeq Acc Id: NR_163392
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3811215,030 - 236,931 (-)NCBI
T2T-CHM13v2.011256,228 - 277,937 (-)NCBI
Sequence:
RefSeq Acc Id: NR_163393
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3811215,030 - 236,931 (-)NCBI
T2T-CHM13v2.011256,228 - 277,937 (-)NCBI
Sequence:
RefSeq Acc Id: NR_163394
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3811215,030 - 236,342 (-)NCBI
T2T-CHM13v2.011256,228 - 277,334 (-)NCBI
Sequence:
RefSeq Acc Id: NR_163395
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3811215,030 - 236,342 (-)NCBI
T2T-CHM13v2.011256,228 - 277,334 (-)NCBI
Sequence:
RefSeq Acc Id: NR_163396
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3811215,030 - 236,342 (-)NCBI
T2T-CHM13v2.011256,228 - 277,334 (-)NCBI
Sequence:
RefSeq Acc Id: NR_163397
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3811215,030 - 236,342 (-)NCBI
T2T-CHM13v2.011256,228 - 277,334 (-)NCBI
Sequence:
RefSeq Acc Id: NR_163398
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3811215,030 - 236,342 (-)NCBI
T2T-CHM13v2.011256,228 - 277,334 (-)NCBI
Sequence:
RefSeq Acc Id: NR_163399
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3811215,030 - 236,342 (-)NCBI
T2T-CHM13v2.011256,228 - 277,334 (-)NCBI
Sequence:
RefSeq Acc Id: NR_163400
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3811215,030 - 236,342 (-)NCBI
T2T-CHM13v2.011256,228 - 277,334 (-)NCBI
Sequence:
RefSeq Acc Id: NR_163401
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3811215,030 - 236,342 (-)NCBI
T2T-CHM13v2.011256,228 - 277,334 (-)NCBI
Sequence:
RefSeq Acc Id: NR_163402
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3811215,030 - 236,342 (-)NCBI
T2T-CHM13v2.011256,228 - 277,334 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011519956   ⟹   XP_011518258
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3811215,030 - 235,554 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011519957   ⟹   XP_011518259
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3811215,030 - 235,554 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017017431   ⟹   XP_016872920
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3811215,030 - 236,342 (-)NCBI
Sequence:
RefSeq Acc Id: XM_047426677   ⟹   XP_047282633
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3811215,030 - 236,342 (-)NCBI
RefSeq Acc Id: XM_054368236   ⟹   XP_054224211
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.011256,228 - 277,033 (-)NCBI
RefSeq Acc Id: XM_054368237   ⟹   XP_054224212
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.011256,228 - 277,033 (-)NCBI
RefSeq Acc Id: XM_054368238   ⟹   XP_054224213
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.011256,228 - 277,340 (-)NCBI
RefSeq Acc Id: XM_054368239   ⟹   XP_054224214
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.011256,228 - 277,365 (-)NCBI
RefSeq Acc Id: XR_007062467
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3811224,078 - 236,342 (-)NCBI
RefSeq Acc Id: XR_008488374
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.011265,059 - 277,334 (-)NCBI
Protein Sequences
Protein RefSeqs NP_001017524 (Get FASTA)   NCBI Sequence Viewer  
  NP_001357239 (Get FASTA)   NCBI Sequence Viewer  
  NP_001357241 (Get FASTA)   NCBI Sequence Viewer  
  NP_001357243 (Get FASTA)   NCBI Sequence Viewer  
  NP_001357244 (Get FASTA)   NCBI Sequence Viewer  
  NP_001357245 (Get FASTA)   NCBI Sequence Viewer  
  NP_001357246 (Get FASTA)   NCBI Sequence Viewer  
  NP_001357247 (Get FASTA)   NCBI Sequence Viewer  
  NP_001357248 (Get FASTA)   NCBI Sequence Viewer  
  NP_001357249 (Get FASTA)   NCBI Sequence Viewer  
  NP_001357250 (Get FASTA)   NCBI Sequence Viewer  
  NP_001357251 (Get FASTA)   NCBI Sequence Viewer  
  NP_001357252 (Get FASTA)   NCBI Sequence Viewer  
  NP_001357253 (Get FASTA)   NCBI Sequence Viewer  
  NP_001357254 (Get FASTA)   NCBI Sequence Viewer  
  NP_036371 (Get FASTA)   NCBI Sequence Viewer  
  XP_011518258 (Get FASTA)   NCBI Sequence Viewer  
  XP_011518259 (Get FASTA)   NCBI Sequence Viewer  
  XP_016872920 (Get FASTA)   NCBI Sequence Viewer  
  XP_047282633 (Get FASTA)   NCBI Sequence Viewer  
  XP_054224211 (Get FASTA)   NCBI Sequence Viewer  
  XP_054224212 (Get FASTA)   NCBI Sequence Viewer  
  XP_054224213 (Get FASTA)   NCBI Sequence Viewer  
  XP_054224214 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAD40851 (Get FASTA)   NCBI Sequence Viewer  
  AAH01042 (Get FASTA)   NCBI Sequence Viewer  
  BAH12816 (Get FASTA)   NCBI Sequence Viewer  
  BAH12927 (Get FASTA)   NCBI Sequence Viewer  
  BAH13032 (Get FASTA)   NCBI Sequence Viewer  
  BAH13513 (Get FASTA)   NCBI Sequence Viewer  
  BAH13600 (Get FASTA)   NCBI Sequence Viewer  
  BAH14546 (Get FASTA)   NCBI Sequence Viewer  
  CAB70674 (Get FASTA)   NCBI Sequence Viewer  
  CAL00156 (Get FASTA)   NCBI Sequence Viewer  
  CAL00157 (Get FASTA)   NCBI Sequence Viewer  
  CAL48199 (Get FASTA)   NCBI Sequence Viewer  
  CAN36293 (Get FASTA)   NCBI Sequence Viewer  
  EAW61239 (Get FASTA)   NCBI Sequence Viewer  
  EAW61240 (Get FASTA)   NCBI Sequence Viewer  
  EAW61241 (Get FASTA)   NCBI Sequence Viewer  
  EAW61242 (Get FASTA)   NCBI Sequence Viewer  
  EAW61243 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000372191
  ENSP00000372191.4
  ENSP00000432857.1
  ENSP00000432937
  ENSP00000432937.1
  ENSP00000433077
  ENSP00000433077.1
  ENSP00000433132.1
  ENSP00000433899.1
  ENSP00000434747.1
  ENSP00000435014.1
  ENSP00000435464
  ENSP00000435464.1
  ENSP00000435505.1
  ENSP00000436085.1
  ENSP00000437179.1
  ENSP00000437216
  ENSP00000437216.1
GenBank Protein Q9NTG7 (Get FASTA)   NCBI Sequence Viewer  
RefSeq Acc Id: NP_001017524   ⟸   NM_001017524
- Peptide Label: isoform b
- UniProtKB: B7ZA60 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_036371   ⟸   NM_012239
- Peptide Label: isoform a
- UniProtKB: B7Z5U6 (UniProtKB/Swiss-Prot),   Q9Y6E8 (UniProtKB/Swiss-Prot),   Q9NTG7 (UniProtKB/Swiss-Prot),   B7Z7G4 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011518259   ⟸   XM_011519957
- Peptide Label: isoform X1
- UniProtKB: B7ZA60 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011518258   ⟸   XM_011519956
- Peptide Label: isoform X1
- UniProtKB: B7ZA60 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016872920   ⟸   XM_017017431
- Peptide Label: isoform X1
- UniProtKB: B7ZA60 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001357253   ⟸   NM_001370324
- Peptide Label: isoform j
RefSeq Acc Id: NP_001357249   ⟸   NM_001370320
- Peptide Label: isoform b
- UniProtKB: B7ZA60 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001357248   ⟸   NM_001370319
- Peptide Label: isoform b
- UniProtKB: B7ZA60 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001357246   ⟸   NM_001370317
- Peptide Label: isoform h
RefSeq Acc Id: NP_001357251   ⟸   NM_001370322
- Peptide Label: isoform i
- UniProtKB: B7ZA60 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001357247   ⟸   NM_001370318
- Peptide Label: isoform b
- UniProtKB: B7ZA60 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001357250   ⟸   NM_001370321
- Peptide Label: isoform i
- UniProtKB: B7ZA60 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001357245   ⟸   NM_001370316
- Peptide Label: isoform g precursor
RefSeq Acc Id: NP_001357244   ⟸   NM_001370315
- Peptide Label: isoform f precursor
- UniProtKB: E9PK80 (UniProtKB/TrEMBL),   B7Z580 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001357254   ⟸   NM_001370325
- Peptide Label: isoform j
RefSeq Acc Id: NP_001357252   ⟸   NM_001370323
- Peptide Label: isoform i
- UniProtKB: B7ZA60 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001357241   ⟸   NM_001370312
- Peptide Label: isoform d
- UniProtKB: E9PN58 (UniProtKB/TrEMBL),   B7Z777 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001357243   ⟸   NM_001370314
- Peptide Label: isoform e
- UniProtKB: E9PM75 (UniProtKB/TrEMBL),   B7Z5J1 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001357239   ⟸   NM_001370310
- Peptide Label: isoform c
- UniProtKB: B7Z7G4 (UniProtKB/TrEMBL)
RefSeq Acc Id: ENSP00000435014   ⟸   ENST00000530067
RefSeq Acc Id: ENSP00000433077   ⟸   ENST00000532956
RefSeq Acc Id: ENSP00000433899   ⟸   ENST00000532837
RefSeq Acc Id: ENSP00000432937   ⟸   ENST00000524564
RefSeq Acc Id: ENSP00000435464   ⟸   ENST00000525319
RefSeq Acc Id: ENSP00000436085   ⟸   ENST00000525237
RefSeq Acc Id: ENSP00000433132   ⟸   ENST00000525776
RefSeq Acc Id: ENSP00000435505   ⟸   ENST00000526854
RefSeq Acc Id: ENSP00000432857   ⟸   ENST00000528469
RefSeq Acc Id: ENSP00000372191   ⟸   ENST00000382743
RefSeq Acc Id: ENSP00000437216   ⟸   ENST00000529382
RefSeq Acc Id: ENSP00000434747   ⟸   ENST00000529937
RefSeq Acc Id: ENSP00000437179   ⟸   ENST00000529055
RefSeq Acc Id: XP_047282633   ⟸   XM_047426677
- Peptide Label: isoform X2
- UniProtKB: B7ZA60 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054224214   ⟸   XM_054368239
- Peptide Label: isoform X2
- UniProtKB: B7ZA60 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054224213   ⟸   XM_054368238
- Peptide Label: isoform X1
- UniProtKB: B7ZA60 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054224211   ⟸   XM_054368236
- Peptide Label: isoform X1
- UniProtKB: B7ZA60 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054224212   ⟸   XM_054368237
- Peptide Label: isoform X1
- UniProtKB: B7ZA60 (UniProtKB/TrEMBL)
Protein Domains
Deacetylase sirtuin-type

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q9NTG7-F1-model_v2 AlphaFold Q9NTG7 1-399 view protein structure

Promoters
RGD ID:6788776
Promoter ID:HG_KWN:11805
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   HeLa_S3,   K562,   Lymphoblastoid,   NB4
Transcripts:ENST00000324945,   NM_001017524,   OTTHUMT00000239288,   UC009YBT.1
Position:
Human AssemblyChrPosition (strand)Source
Build 3611226,141 - 227,607 (-)MPROMDB
RGD ID:7219103
Promoter ID:EPDNEW_H15298
Type:multiple initiation site
Name:SIRT3_1
Description:sirtuin 3
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh3811236,342 - 236,402EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:14931 AgrOrtholog
COSMIC SIRT3 COSMIC
Ensembl Genes ENSG00000142082 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000382743 ENTREZGENE
  ENST00000382743.9 UniProtKB/Swiss-Prot
  ENST00000524564 ENTREZGENE
  ENST00000524564.5 UniProtKB/TrEMBL
  ENST00000525237.1 UniProtKB/TrEMBL
  ENST00000525319 ENTREZGENE
  ENST00000525319.5 UniProtKB/TrEMBL
  ENST00000525776.1 UniProtKB/TrEMBL
  ENST00000526854.5 UniProtKB/TrEMBL
  ENST00000528469.1 UniProtKB/TrEMBL
  ENST00000529055.5 UniProtKB/TrEMBL
  ENST00000529382 ENTREZGENE
  ENST00000529382.5 UniProtKB/Swiss-Prot
  ENST00000529937.1 UniProtKB/TrEMBL
  ENST00000530067.1 UniProtKB/TrEMBL
  ENST00000532837.5 UniProtKB/TrEMBL
  ENST00000532956 ENTREZGENE
  ENST00000532956.5 UniProtKB/TrEMBL
Gene3D-CATH 3.30.1600.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  TPP-binding domain UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000142082 GTEx
HGNC ID HGNC:14931 ENTREZGENE
Human Proteome Map SIRT3 Human Proteome Map
InterPro DHS-like_NAD/FAD-binding_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Sirtuin UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Sirtuin_cat_small_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Sirtuin_class_I UniProtKB/TrEMBL
  Ssirtuin_cat_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:23410 UniProtKB/Swiss-Prot
NCBI Gene 23410 ENTREZGENE
OMIM 604481 OMIM
PANTHER NAD-DEPENDENT PROTEIN DEACETYLASE SIRTUIN-3, MITOCHONDRIAL UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  NAD-DEPENDENT PROTEIN DEACYLASE SIRTUIN-5, MITOCHONDRIAL-RELATED UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam SIR2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA37936 PharmGKB
PIRSF SIR2_euk UniProtKB/TrEMBL
PROSITE SIRTUIN UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF52467 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt B7WNN4_HUMAN UniProtKB/TrEMBL
  B7Z580 ENTREZGENE, UniProtKB/TrEMBL
  B7Z5J1 ENTREZGENE, UniProtKB/TrEMBL
  B7Z5U6 ENTREZGENE
  B7Z777 ENTREZGENE, UniProtKB/TrEMBL
  B7Z7G4 ENTREZGENE, UniProtKB/TrEMBL
  B7ZA60 ENTREZGENE, UniProtKB/TrEMBL
  E9PIT6_HUMAN UniProtKB/TrEMBL
  E9PJS6_HUMAN UniProtKB/TrEMBL
  E9PK80 ENTREZGENE, UniProtKB/TrEMBL
  E9PM52_HUMAN UniProtKB/TrEMBL
  E9PM75 ENTREZGENE, UniProtKB/TrEMBL
  E9PN58 ENTREZGENE, UniProtKB/TrEMBL
  E9PNA0_HUMAN UniProtKB/TrEMBL
  E9PR48_HUMAN UniProtKB/TrEMBL
  Q9NTG7 ENTREZGENE
  Q9Y6E8 ENTREZGENE
  SIR3_HUMAN UniProtKB/Swiss-Prot
UniProt Secondary B7Z5U6 UniProtKB/Swiss-Prot
  Q9Y6E8 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2011-07-27 SIRT3  sirtuin 3  SIRT3  sirtuin (silent mating type information regulation 2 homolog) 3 (S. cerevisiae)  Symbol and/or name change 5135510 APPROVED