NAMPT (nicotinamide phosphoribosyltransferase) - Rat Genome Database

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Gene: NAMPT (nicotinamide phosphoribosyltransferase) Homo sapiens
Analyze
Symbol: NAMPT
Name: nicotinamide phosphoribosyltransferase
RGD ID: 1351636
HGNC Page HGNC:30092
Description: Enables identical protein binding activity. Involved in positive regulation of nitric-oxide synthase biosynthetic process and positive regulation of transcription by RNA polymerase II. Located in cell junction and nuclear speck. Implicated in transient cerebral ischemia. Biomarker of artery disease (multiple); obesity; psoriasis; and type 2 diabetes mellitus.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: 1110035O14Rik; DKFZp666B131; MGC117256; NAmPRTase; PBEF; PBEF1; pre-B cell-enhancing factor; pre-B-cell colony enhancing factor 1; pre-B-cell colony-enhancing factor 1; VF; VISFATIN
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Related Pseudogenes: NAMPTP1   NAMPTP2   NAMPTP3  
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh387106,248,298 - 106,285,888 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl7106,248,298 - 106,285,966 (-)EnsemblGRCh38hg38GRCh38
GRCh377105,888,744 - 105,925,429 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 367105,675,967 - 105,712,874 (-)NCBINCBI36Build 36hg18NCBI36
Build 347105,495,899 - 105,519,318NCBI
Celera7100,694,260 - 100,731,169 (-)NCBICelera
Cytogenetic Map7q22.3NCBI
HuRef7100,248,062 - 100,285,253 (-)NCBIHuRef
CHM1_17105,822,212 - 105,859,137 (-)NCBICHM1_1
T2T-CHM13v2.07107,563,712 - 107,602,631 (-)NCBIT2T-CHM13v2.0
CRA_TCAGchr7v27105,249,752 - 105,286,646 (-)NCBI
JBrowse: View Region in Genome Browser (JBrowse)
Model


Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
(-)-alpha-phellandrene  (EXP)
(-)-demecolcine  (EXP)
(S)-amphetamine  (ISO)
(S)-nicotine  (ISO)
1,2-dichloroethane  (ISO)
1,2-dimethylhydrazine  (ISO)
1-chloro-2,4-dinitrobenzene  (EXP)
1-fluoro-2,4-dinitrobenzene  (EXP)
1-methylnicotinamide  (ISO)
14-Deoxy-11,12-didehydroandrographolide  (EXP)
17alpha-ethynylestradiol  (ISO)
17beta-estradiol  (EXP,ISO)
2,2',4,4',5,5'-hexachlorobiphenyl  (ISO)
2,3,7,8-tetrachlorodibenzodioxine  (EXP,ISO)
2,3,7,8-Tetrachlorodibenzofuran  (ISO)
2-acetamidofluorene  (ISO)
2-hydroxypropanoic acid  (EXP)
2-methoxyethanol  (ISO)
3,3',4,4',5-pentachlorobiphenyl  (ISO)
3,3',4,4'-tetrachlorobiphenyl  (ISO)
3-chloropropane-1,2-diol  (ISO)
3-isobutyl-1-methyl-7H-xanthine  (ISO)
4,4'-diaminodiphenylmethane  (ISO)
4,4'-sulfonyldiphenol  (EXP)
4-(ethoxymethylene)-2-phenyloxazol-5-one  (EXP)
6-chloro-2,3,4,9-tetrahydro-1H-carbazole-1-carboxamide  (EXP)
acetic acid  (ISO)
aflatoxin B1  (EXP)
aldehydo-D-glucose  (EXP)
all-trans-retinoic acid  (EXP)
alpha-phellandrene  (EXP)
ammonium chloride  (ISO)
ammonium hexachloroplatinate  (EXP)
antirheumatic drug  (EXP)
aristolochic acid A  (EXP)
arsenite(3-)  (EXP)
arsenous acid  (EXP)
azoxystrobin  (EXP)
benzene  (EXP)
benzo[a]pyrene  (EXP,ISO)
benzo[a]pyrene diol epoxide I  (EXP)
benzofurans  (ISO)
berberine  (EXP)
bis(2-chloroethyl) sulfide  (ISO)
bis(2-ethylhexyl) phthalate  (ISO)
bisphenol A  (EXP,ISO)
Bisphenol B  (EXP)
bisphenol F  (EXP)
bromobenzene  (ISO)
Butylbenzyl phthalate  (ISO)
cadmium atom  (EXP,ISO)
cadmium dichloride  (EXP,ISO)
calcitriol  (EXP)
carbamazepine  (EXP)
carbon nanotube  (ISO)
carteolol  (EXP)
CGP 52608  (EXP)
CHIR 99021  (EXP)
chlorendic acid  (ISO)
chloroacetaldehyde  (EXP)
chlorohydrocarbon  (ISO)
chloroprene  (ISO)
chlorpromazine  (ISO)
chlorpyrifos  (ISO)
cidofovir anhydrous  (EXP)
cisplatin  (EXP)
cobalt dichloride  (ISO)
copper(II) sulfate  (EXP)
crocidolite asbestos  (EXP)
cyclophosphamide  (ISO)
cyclosporin A  (EXP)
D-glucose  (EXP)
decabromodiphenyl ether  (ISO)
deguelin  (EXP)
deoxynivalenol  (EXP)
dexamethasone  (EXP,ISO)
diarsenic trioxide  (EXP)
diazoxide  (EXP)
dibenz[a,h]anthracene  (ISO)
dibutyl phthalate  (ISO)
dichloromethane  (ISO)
dicrotophos  (EXP)
dieldrin  (ISO)
diethylstilbestrol  (ISO)
dimethylarsinous acid  (EXP)
dioxygen  (EXP,ISO)
disodium selenite  (EXP)
divanadium pentaoxide  (EXP)
doxorubicin  (EXP)
endosulfan  (ISO)
epoxiconazole  (ISO)
estriol  (ISO)
ethylbenzene  (EXP)
eugenol  (EXP)
fenofibrate  (ISO)
finasteride  (ISO)
flutamide  (ISO)
folic acid  (ISO)
furan  (ISO)
gentamycin  (ISO)
glucose  (EXP)
hydralazine  (EXP)
hydroxyurea  (ISO)
ibuprofen  (EXP)
isotretinoin  (EXP)
ivermectin  (EXP)
L-ascorbic acid  (ISO)
lead(0)  (EXP)
leflunomide  (EXP)
letrozole  (ISO)
levofloxacin  (ISO)
lipopolysaccharide  (EXP)
manganese atom  (EXP)
manganese(0)  (EXP)
manganese(II) chloride  (EXP)
metformin  (EXP,ISO)
methamphetamine  (ISO)
methotrexate  (EXP,ISO)
methylmercury chloride  (ISO)
mitoxantrone  (EXP)
NAD zwitterion  (EXP,ISO)
NAD(+)  (EXP,ISO)
nefazodone  (ISO)
nevirapine  (ISO)
nickel atom  (EXP)
nickel dichloride  (ISO)
nickel sulfate  (EXP)
nicotinamide  (EXP,ISO)
nicotine  (ISO)
nifedipine  (EXP)
nimesulide  (ISO)
NMN zwitterion  (EXP,ISO)
p-anisidine  (ISO)
paclitaxel  (EXP,ISO)
paraquat  (ISO)
parathion  (ISO)
pentachlorophenol  (ISO)
perfluorohexanesulfonic acid  (ISO)
perfluorooctane-1-sulfonic acid  (EXP)
phenobarbital  (ISO)
picoxystrobin  (EXP)
progesterone  (EXP,ISO)
quinoline  (EXP)
rac-lactic acid  (EXP)
reactive oxygen species  (EXP)
resveratrol  (EXP,ISO)
rotenone  (EXP)
S-(1,2-dichlorovinyl)-L-cysteine  (EXP)
sodium arsenite  (EXP)
sodium dichromate  (ISO)
streptozocin  (ISO)
sulindac  (ISO)
sunitinib  (EXP)
tamoxifen  (ISO)
tanespimycin  (EXP)
temozolomide  (EXP)
testosterone  (EXP,ISO)
tetrachloromethane  (ISO)
tetrathiomolybdate(2-)  (EXP)
thapsigargin  (ISO)
thiram  (EXP)
Tolmetin glucuronide  (EXP)
toluene  (EXP)
tributylstannane  (EXP)
trichloroethene  (ISO)
trichostatin A  (EXP)
triphenylstannane  (EXP)
Triptolide  (ISO)
troglitazone  (EXP)
uranium atom  (EXP)
valproic acid  (EXP,ISO)
vinclozolin  (ISO)
vincristine  (EXP)
vorinostat  (EXP)
zinc atom  (ISO)
zinc(0)  (ISO)
zoledronic acid  (EXP)

Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component

Molecular Function

Molecular Pathway Annotations     Click to see Annotation Detail View
Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
References

References - curated
# Reference Title Reference Citation
1. NAMPT inhibitor protects ischemic neuronal injury in rat brain via anti-neuroinflammation. Chen CX, etal., Neuroscience. 2017 Jul 25;356:193-206. doi: 10.1016/j.neuroscience.2017.05.022. Epub 2017 May 19.
2. Nicotinamide Phosphoribosyltransferase Promotes Pulmonary Vascular Remodeling and Is a Therapeutic Target in Pulmonary Arterial Hypertension. Chen J, etal., Circulation. 2017 Apr 18;135(16):1532-1546. doi: 10.1161/CIRCULATIONAHA.116.024557. Epub 2017 Feb 15.
3. Elevated plasma level of visfatin/pre-B cell colony-enhancing factor in patients with type 2 diabetes mellitus. Chen MP, etal., J Clin Endocrinol Metab. 2006 Jan;91(1):295-9. Epub 2005 Oct 18.
4. Increased expression of visfatin in macrophages of human unstable carotid and coronary atherosclerosis: possible role in inflammation and plaque destabilization. Dahl TB, etal., Circulation. 2007 Feb 27;115(8):972-80. Epub 2007 Feb 5.
5. Nampt/PBEF/visfatin exerts neuroprotective effects against ischemia/reperfusion injury via modulation of Bax/Bcl-2 ratio and prevention of caspase-3 activation. Erfani S, etal., J Mol Neurosci. 2015 May;56(1):237-43. doi: 10.1007/s12031-014-0486-1. Epub 2015 Jan 22.
6. Increased plasma levels of visfatin/pre-B cell colony-enhancing factor in obese and overweight patients with metabolic syndrome. Filippatos TD, etal., J Endocrinol Invest. 2007 Apr;30(4):323-6.
7. Leptin, adiponectin, visfatin and retinol-binding protein-4 - mediators of comorbidities in patients with psoriasis? Gerdes S, etal., Exp Dermatol. 2012 Jan;21(1):43-7. doi: 10.1111/j.1600-0625.2011.01402.x.
8. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
9. The secret life of NAD+: an old metabolite controlling new metabolic signaling pathways. Houtkooper RH, etal., Endocr Rev. 2010 Apr;31(2):194-223. doi: 10.1210/er.2009-0026. Epub 2009 Dec 9.
10. Hyperbaric Oxygen Reduces Infarction Volume and Hemorrhagic Transformation Through ATP/NAD+/Sirt1 Pathway in Hyperglycemic Middle Cerebral Artery Occlusion Rats. Hu Q, etal., Stroke. 2017 Jun;48(6):1655-1664. doi: 10.1161/STROKEAHA.116.015753. Epub 2017 May 11.
11. Visfatin: gene expression in isolated adipocytes and sequence analysis in obese WOKW rats compared with lean control rats. Kloting N and Kloting I, Biochem Biophys Res Commun. 2005 Jul 15;332(4):1070-2.
12. Serum visfatin in relation to insulin resistance and markers of hyperandrogenism in lean and obese women with polycystic ovary syndrome. Kowalska I, etal., Hum Reprod. 2007 Jul;22(7):1824-9.
13. Effect of curcumin on visfatin and zinc-α2-glycoprotein in a rat model of non-alcoholic fatty liver disease. Li C, etal., Acta Cir Bras. 2016 Nov;31(11):706-713. doi: 10.1590/S0102-865020160110000001.
14. Periodontitis contributes to aberrant metabolism in type 2 diabetes mellitus rats by stimulating the expression of adipokines. Luo S, etal., J Periodontal Res. 2016 Aug;51(4):453-61. doi: 10.1111/jre.12322. Epub 2015 Oct 12.
15. Protective effect of P7C3 on retinal ganglion cells from optic nerve injury. Oku H, etal., Jpn J Ophthalmol. 2017 Mar;61(2):195-203. doi: 10.1007/s10384-016-0493-6. Epub 2016 Dec 28.
16. KEGG Annotation Import Pipeline Pipeline to import KEGG annotations from KEGG into RGD
17. SMPDB Annotation Import Pipeline Pipeline to import SMPDB annotations from SMPDB into RGD
18. Correlation of circulating full-length visfatin (PBEF/NAMPT) with metabolic parameters in subjects with and without diabetes: a cross-sectional study. Retnakaran R, etal., Clin Endocrinol (Oxf). 2008 Dec;69(6):885-93. Epub 2008 Apr 10.
19. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
20. Sleep restriction induced energy, methylation and lipogenesis metabolic switches in rat liver. Sengupta A, etal., Int J Biochem Cell Biol. 2017 Dec;93:129-135. doi: 10.1016/j.biocel.2017.08.014. Epub 2017 Aug 30.
21. Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. Strausberg RL, etal., Proc Natl Acad Sci U S A. 2002 Dec 24;99(26):16899-903. Epub 2002 Dec 11.
22. The renoprotective effect of curcumin in cisplatin-induced nephrotoxicity. Ugur S, etal., Ren Fail. 2015 Mar;37(2):332-6. doi: 10.3109/0886022X.2014.986005. Epub 2015 Jan 16.
23. Immune cell profiling of COVID-19 patients in the recovery stage by single-cell sequencing. Wen W, etal., Cell Discov. 2020 May 4;6:31. doi: 10.1038/s41421-020-0168-9. eCollection 2020.
24. Serum concentration of visfatin in obese women. Zahorska-Markiewicz B, etal., Metabolism. 2007 Aug;56(8):1131-4.
25. Heightened Innate Immune Responses in the Respiratory Tract of COVID-19 Patients. Zhou Z, etal., Cell Host Microbe. 2020 Jun 10;27(6):883-890.e2. doi: 10.1016/j.chom.2020.04.017. Epub 2020 May 4.
Additional References at PubMed
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PMID:27023106   PMID:27025967   PMID:27058759   PMID:27074203   PMID:27126198   PMID:27128025   PMID:27166432   PMID:27166797   PMID:27190335   PMID:27224551   PMID:27233476   PMID:27287071  
PMID:27421003   PMID:27491149   PMID:27525051   PMID:27566659   PMID:27568842   PMID:27712122   PMID:27732642   PMID:27770715   PMID:27792999   PMID:27884778   PMID:27887573   PMID:28010141  
PMID:28025432   PMID:28031328   PMID:28044053   PMID:28073026   PMID:28097126   PMID:28168205   PMID:28178643   PMID:28205390   PMID:28240682   PMID:28276108   PMID:28319085   PMID:28356339  
PMID:28378594   PMID:28408371   PMID:28416276   PMID:28442350   PMID:28468779   PMID:28482725   PMID:28507103   PMID:28514442   PMID:28515276   PMID:28561026   PMID:28667355   PMID:28677720  
PMID:28677752   PMID:28699485   PMID:28714034   PMID:28756225   PMID:28762597   PMID:28819322   PMID:28837586   PMID:28860121   PMID:28870901   PMID:28919418   PMID:28977470   PMID:29053956  
PMID:29101068   PMID:29105498   PMID:29128334   PMID:29203587   PMID:29228527   PMID:29277835   PMID:29309612   PMID:29331416   PMID:29337272   PMID:29337590   PMID:29355093   PMID:29467282  
PMID:29516012   PMID:29546048   PMID:29567766   PMID:29601800   PMID:29769421   PMID:29808800   PMID:29886033   PMID:29955894   PMID:30001864   PMID:30033366   PMID:30121947   PMID:30182136  
PMID:30184561   PMID:30191976   PMID:30206161   PMID:30224938   PMID:30256660   PMID:30261504   PMID:30318936   PMID:30349055   PMID:30463229   PMID:30463901   PMID:30471099   PMID:30483779  
PMID:30514106   PMID:30541001   PMID:30563239   PMID:30575818   PMID:30799084   PMID:30833792   PMID:30856230   PMID:30892950   PMID:30948266   PMID:30952715   PMID:30963978   PMID:31022738  
PMID:31025138   PMID:31026096   PMID:31076892   PMID:31091453   PMID:31132798   PMID:31177228   PMID:31204283   PMID:31235138   PMID:31322259   PMID:31372850   PMID:31452406   PMID:31487747  
PMID:31588856   PMID:31710121   PMID:31717318   PMID:31771561   PMID:31900828   PMID:31940881   PMID:31957305   PMID:32060556   PMID:32087970   PMID:32098202   PMID:32107941   PMID:32142369  
PMID:32176739   PMID:32243098   PMID:32252104   PMID:32296183   PMID:32311618   PMID:32390008   PMID:32416067   PMID:32423001   PMID:32460545   PMID:32466159   PMID:32495871   PMID:32503436  
PMID:32597148   PMID:32618342   PMID:32681594   PMID:32687490   PMID:32694731   PMID:32807821   PMID:32807901   PMID:32963011   PMID:32994395   PMID:33029930   PMID:33045468   PMID:33122129  
PMID:33239621   PMID:33247685   PMID:33356858   PMID:33432364   PMID:33462405   PMID:33488923   PMID:33513808   PMID:33540574   PMID:33543238   PMID:33567341   PMID:33568815   PMID:33626391  
PMID:33649309   PMID:33658012   PMID:33742100   PMID:33766124   PMID:33816632   PMID:33823623   PMID:33901513   PMID:33916271   PMID:33944612   PMID:33961781   PMID:33975612   PMID:33976173  
PMID:34070254   PMID:34079125   PMID:34101492   PMID:34139379   PMID:34201564   PMID:34202251   PMID:34360874   PMID:34373451   PMID:34439776   PMID:34445345   PMID:34551033   PMID:34626279  
PMID:34645483   PMID:34656559   PMID:34709727   PMID:34717061   PMID:34748530   PMID:34780058   PMID:34967693   PMID:35013218   PMID:35111160   PMID:35120922   PMID:35227662   PMID:35241646  
PMID:35256949   PMID:35271311   PMID:35384245   PMID:35439318   PMID:35451654   PMID:35466629   PMID:35509820   PMID:35545034   PMID:35562734   PMID:35628596   PMID:35661560   PMID:35681168  
PMID:35809287   PMID:35831314   PMID:35839539   PMID:36114006   PMID:36180527   PMID:36215168   PMID:36244648   PMID:36321597   PMID:36429891   PMID:36432602   PMID:36540014   PMID:36653284  
PMID:36658296   PMID:37105926   PMID:37175698   PMID:37199515   PMID:37246238   PMID:37329710   PMID:37356938   PMID:37370246   PMID:37512089   PMID:37512134   PMID:37545421   PMID:37556846  
PMID:37679252   PMID:37689310   PMID:37730614   PMID:37827155   PMID:37884188   PMID:38095401   PMID:38155161   PMID:38216702   PMID:38252081   PMID:38387912  


Genomics

Comparative Map Data
NAMPT
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh387106,248,298 - 106,285,888 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl7106,248,298 - 106,285,966 (-)EnsemblGRCh38hg38GRCh38
GRCh377105,888,744 - 105,925,429 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 367105,675,967 - 105,712,874 (-)NCBINCBI36Build 36hg18NCBI36
Build 347105,495,899 - 105,519,318NCBI
Celera7100,694,260 - 100,731,169 (-)NCBICelera
Cytogenetic Map7q22.3NCBI
HuRef7100,248,062 - 100,285,253 (-)NCBIHuRef
CHM1_17105,822,212 - 105,859,137 (-)NCBICHM1_1
T2T-CHM13v2.07107,563,712 - 107,602,631 (-)NCBIT2T-CHM13v2.0
CRA_TCAGchr7v27105,249,752 - 105,286,646 (-)NCBI
Nampt
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391232,870,334 - 32,903,368 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1232,869,544 - 32,903,348 (+)EnsemblGRCm39 Ensembl
GRCm381232,820,335 - 32,853,369 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1232,819,545 - 32,853,349 (+)EnsemblGRCm38mm10GRCm38
MGSCv371233,505,200 - 33,538,234 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361233,405,722 - 33,436,855 (+)NCBIMGSCv36mm8
Celera1234,264,778 - 34,297,952 (+)NCBICelera
Cytogenetic Map12A3NCBI
cM Map1213.74NCBI
Nampt
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr8655,152,756 - 55,189,547 (+)NCBIGRCr8
mRatBN7.2649,425,316 - 49,462,109 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl649,424,332 - 49,462,100 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx649,728,050 - 49,763,075 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0650,042,969 - 50,077,994 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0649,480,294 - 49,514,732 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.0652,122,085 - 52,156,473 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl652,122,085 - 52,156,472 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.0661,753,125 - 61,787,575 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4651,129,160 - 51,166,514 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.1651,132,285 - 51,169,639 (+)NCBI
Celera648,619,485 - 48,654,540 (+)NCBICelera
Cytogenetic Map6q16NCBI
Nampt
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495541010,717,664 - 10,751,177 (-)EnsemblChiLan1.0
ChiLan1.0NW_00495541010,717,664 - 10,742,109 (-)NCBIChiLan1.0ChiLan1.0
NAMPT
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v26143,085,389 - 143,122,843 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan17191,355,357 - 191,392,827 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v0798,227,071 - 98,262,254 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.17110,952,876 - 110,989,233 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl7110,952,876 - 110,981,967 (-)Ensemblpanpan1.1panPan2
NAMPT
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.11814,110,045 - 14,211,268 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl1813,993,022 - 14,208,657 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha1813,815,825 - 13,860,578 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.01814,441,923 - 14,486,695 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl1814,441,184 - 14,486,688 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.11814,254,107 - 14,298,642 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.01814,175,231 - 14,219,981 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.01814,455,285 - 14,500,038 (+)NCBIUU_Cfam_GSD_1.0
Nampt
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440511856,558,385 - 56,593,898 (+)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_00493647917,682,201 - 17,716,661 (+)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_00493647917,682,070 - 17,716,713 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
NAMPT
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl9106,119,899 - 106,294,586 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.19106,119,896 - 106,162,126 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.29116,889,082 - 116,932,047 (-)NCBISscrofa10.2Sscrofa10.2susScr3
NAMPT
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.12175,160,748 - 75,195,781 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl2175,158,596 - 75,196,025 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366604228,713,073 - 28,750,454 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Nampt
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_00462473923,411,488 - 23,442,359 (+)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_00462473923,411,478 - 23,444,590 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in NAMPT
10 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 7q22.1-31.1(chr7:101807149-112414850)x1 copy number loss See cases [RCV000050924] Chr7:101807149..112414850 [GRCh38]
Chr7:101450429..112054905 [GRCh37]
Chr7:101237149..111842141 [NCBI36]
Chr7:7q22.1-31.1		 pathogenic
GRCh38/hg38 7p22.3-q36.3(chr7:53985-159282531)x1 copy number loss See cases [RCV000052250] Chr7:53985..159282531 [GRCh38]
Chr7:53985..159075220 [GRCh37]
Chr7:149068..158767981 [NCBI36]
Chr7:7p22.3-q36.3		 pathogenic
GRCh38/hg38 7q22.3-31.1(chr7:106261939-111228036)x1 copy number loss See cases [RCV000054158] Chr7:106261939..111228036 [GRCh38]
Chr7:105902385..110868092 [GRCh37]
Chr7:105689621..110655328 [NCBI36]
Chr7:7q22.3-31.1		 pathogenic
GRCh38/hg38 7p22.3-q36.3(chr7:54185-159282390)x1 copy number loss See cases [RCV000135401] Chr7:54185..159282390 [GRCh38]
Chr7:54185..159075079 [GRCh37]
Chr7:149268..158767840 [NCBI36]
Chr7:7p22.3-q36.3		 pathogenic
GRCh38/hg38 7q21.3-36.3(chr7:97419852-158923762)x3 copy number gain See cases [RCV000136717] Chr7:97419852..158923762 [GRCh38]
Chr7:97049164..158716453 [GRCh37]
Chr7:96887100..158409214 [NCBI36]
Chr7:7q21.3-36.3		 pathogenic
GRCh38/hg38 7q22.1-31.31(chr7:102196924-121278641)x1 copy number loss See cases [RCV000137522] Chr7:102196924..121278641 [GRCh38]
Chr7:101912320..120918695 [GRCh37]
Chr7:101626924..120705931 [NCBI36]
Chr7:7q22.1-31.31		 pathogenic
GRCh38/hg38 7q22.3-31.1(chr7:105575647-107949294)x1 copy number loss See cases [RCV000142628] Chr7:105575647..107949294 [GRCh38]
Chr7:105216094..107589739 [GRCh37]
Chr7:105003330..107376975 [NCBI36]
Chr7:7q22.3-31.1		 uncertain significance
TMEM106B-BRAF fusion deletion Pleomorphic xanthoastrocytoma [RCV000454357] Chr7:12258147..140494267 [GRCh37]
Chr7:7p21.3-q34		 pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:43360-159119707)x1 copy number loss See cases [RCV000446044] Chr7:43360..159119707 [GRCh37]
Chr7:7p22.3-q36.3		 pathogenic
GRCh37/hg19 7q22.1-36.3(chr7:98969247-159119707)x3 copy number gain See cases [RCV000447709] Chr7:98969247..159119707 [GRCh37]
Chr7:7q22.1-36.3		 pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:43361-159119707) copy number gain See cases [RCV000510686] Chr7:43361..159119707 [GRCh37]
Chr7:7p22.3-q36.3		 pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:43361-159119707)x3 copy number gain See cases [RCV000511549] Chr7:43361..159119707 [GRCh37]
Chr7:7p22.3-q36.3		 pathogenic
NM_005746.3(NAMPT):c.22G>C (p.Glu8Gln) single nucleotide variant Inborn genetic diseases [RCV003243856] Chr7:106284863 [GRCh38]
Chr7:105925309 [GRCh37]
Chr7:7q22.3		 uncertain significance
GRCh37/hg19 7q22.1-36.3(chr7:98693388-159119707)x3 copy number gain not provided [RCV000682911] Chr7:98693388..159119707 [GRCh37]
Chr7:7q22.1-36.3		 pathogenic
NC_000007.13:g.(20954043_21001537)_(114528369_114556605)inv inversion Childhood apraxia of speech [RCV000234948] Chr7:21001537..114528369 [GRCh37]
Chr7:7p15.3-q31.1		 pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:10704-159122532)x3 copy number gain not provided [RCV000746278] Chr7:10704..159122532 [GRCh37]
Chr7:7p22.3-q36.3		 pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:44935-159126310)x3 copy number gain not provided [RCV000746280] Chr7:44935..159126310 [GRCh37]
Chr7:7p22.3-q36.3		 pathogenic
NM_005746.3(NAMPT):c.1002T>C (p.Val334=) single nucleotide variant not provided [RCV000964133] Chr7:106261675 [GRCh38]
Chr7:105902121 [GRCh37]
Chr7:7q22.3		 benign
GRCh37/hg19 7p22.3-q36.3(chr7:10365-159119707)x3 copy number gain not provided [RCV000848126] Chr7:10365..159119707 [GRCh37]
Chr7:7p22.3-q36.3		 pathogenic
NM_005746.3(NAMPT):c.1366-8T>C single nucleotide variant not provided [RCV000892510] Chr7:106251201 [GRCh38]
Chr7:105891647 [GRCh37]
Chr7:7q22.3		 benign
NM_005746.3(NAMPT):c.201T>C (p.Asn67=) single nucleotide variant not provided [RCV000879166] Chr7:106277036 [GRCh38]
Chr7:105917482 [GRCh37]
Chr7:7q22.3		 benign
GRCh37/hg19 7q22.3-31.1(chr7:104506008-107408857) copy number loss See cases [RCV000993745] Chr7:104506008..107408857 [GRCh37]
Chr7:7q22.3-31.1		 pathogenic
NC_000007.13:g.(?_104456677)_(108155935_?)del deletion not provided [RCV003107618] Chr7:104456677..108155935 [GRCh37]
Chr7:7q22.2-31.1		 pathogenic
NM_005746.3(NAMPT):c.999T>C (p.Pro333=) single nucleotide variant not provided [RCV000954683] Chr7:106261678 [GRCh38]
Chr7:105902124 [GRCh37]
Chr7:7q22.3		 benign
Single allele complex Ring chromosome 7 [RCV002280646] Chr7:43360..159119707 [GRCh37]
Chr7:7p22.3-q36.3		 pathogenic
GRCh37/hg19 7q22.1-31.1(chr7:99417471-111586308) copy number loss not specified [RCV002053711] Chr7:99417471..111586308 [GRCh37]
Chr7:7q22.1-31.1		 pathogenic
GRCh37/hg19 7q22.1-31.31(chr7:100676872-119156160) copy number loss not specified [RCV002053712] Chr7:100676872..119156160 [GRCh37]
Chr7:7q22.1-31.31		 pathogenic
NC_000007.13:g.(?_102937907)_(107643330_?)dup duplication not provided [RCV003113939] Chr7:102937907..107643330 [GRCh37]
Chr7:7q22.1-31.1		 uncertain significance
GRCh37/hg19 7p22.3-q36.3(chr7:56604613-96692931)x1 copy number loss See cases [RCV002287832] Chr7:56604613..96692931 [GRCh37]
Chr7:7p22.3-q36.3		 uncertain significance
NM_005746.3(NAMPT):c.865A>G (p.Lys289Glu) single nucleotide variant Inborn genetic diseases [RCV002762577] Chr7:106263496 [GRCh38]
Chr7:105903942 [GRCh37]
Chr7:7q22.3		 uncertain significance
NM_005746.3(NAMPT):c.1424A>C (p.Glu475Ala) single nucleotide variant Inborn genetic diseases [RCV002978084] Chr7:106251135 [GRCh38]
Chr7:105891581 [GRCh37]
Chr7:7q22.3		 uncertain significance
NM_005746.3(NAMPT):c.802C>A (p.Gln268Lys) single nucleotide variant Inborn genetic diseases [RCV002916524] Chr7:106263559 [GRCh38]
Chr7:105904005 [GRCh37]
Chr7:7q22.3		 uncertain significance
NM_005746.3(NAMPT):c.978G>T (p.Glu326Asp) single nucleotide variant Inborn genetic diseases [RCV003212279] Chr7:106261699 [GRCh38]
Chr7:105902145 [GRCh37]
Chr7:7q22.3		 likely benign
NM_005746.3(NAMPT):c.95A>G (p.Lys32Arg) single nucleotide variant Inborn genetic diseases [RCV003383119] Chr7:106277142 [GRCh38]
Chr7:105917588 [GRCh37]
Chr7:7q22.3		 uncertain significance
GRCh37/hg19 7q22.3-31.1(chr7:104536649-109624996)x1 copy number loss not provided [RCV003482977] Chr7:104536649..109624996 [GRCh37]
Chr7:7q22.3-31.1		 pathogenic
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:1481
Count of miRNA genes:837
Interacting mature miRNAs:980
Transcripts:ENST00000222553, ENST00000354289, ENST00000393618, ENST00000417537, ENST00000424768, ENST00000441045, ENST00000463871, ENST00000467730, ENST00000484527, ENST00000486949, ENST00000489358, ENST00000489732, ENST00000491027
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
RH36790  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371634,323,211 - 34,323,302UniSTSGRCh37
GRCh377105,888,854 - 105,888,945UniSTSGRCh37
Build 367105,676,090 - 105,676,181RGDNCBI36
Celera7100,694,383 - 100,694,474UniSTS
Celera666,708,204 - 66,708,295RGD
Cytogenetic Map7q22.3UniSTS
HuRef1631,077,256 - 31,077,347UniSTS
HuRef7100,248,185 - 100,248,276UniSTS
CRA_TCAGchr7v27105,249,875 - 105,249,966UniSTS
A002U17  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377105,888,884 - 105,889,023UniSTSGRCh37
Build 367105,676,120 - 105,676,259RGDNCBI36
Celera7100,694,413 - 100,694,552RGD
Cytogenetic Map7q22.3UniSTS
HuRef7100,248,215 - 100,248,354UniSTS
CRA_TCAGchr7v27105,249,905 - 105,250,044UniSTS
GeneMap99-GB4 RH Map7527.51UniSTS
D7S2650  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371634,323,204 - 34,323,325UniSTSGRCh37
GRCh377105,888,831 - 105,888,952UniSTSGRCh37
Build 367105,676,067 - 105,676,188RGDNCBI36
Celera7100,694,360 - 100,694,481UniSTS
Celera666,708,197 - 66,708,318RGD
Cytogenetic Map7q22.3UniSTS
HuRef1631,077,249 - 31,077,370UniSTS
HuRef7100,248,162 - 100,248,283UniSTS
CRA_TCAGchr7v27105,249,852 - 105,249,973UniSTS
SHGC-33252  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377105,900,355 - 105,900,482UniSTSGRCh37
Build 367105,687,591 - 105,687,718RGDNCBI36
Celera7100,705,884 - 100,706,011RGD
Cytogenetic Map7q22.3UniSTS
HuRef7100,259,669 - 100,259,796UniSTS
CRA_TCAGchr7v27105,261,359 - 105,261,486UniSTS
TNG Radiation Hybrid Map746144.0UniSTS
GeneMap99-GB4 RH Map7532.41UniSTS
Whitehead-RH Map7484.1UniSTS
GeneMap99-G3 RH Map75173.0UniSTS
RH16541  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377105,900,355 - 105,900,540UniSTSGRCh37
Build 367105,687,591 - 105,687,776RGDNCBI36
Celera7100,705,884 - 100,706,069RGD
Cytogenetic Map7q22.3UniSTS
HuRef7100,259,669 - 100,259,854UniSTS
CRA_TCAGchr7v27105,261,359 - 105,261,544UniSTS
GeneMap99-GB4 RH Map7525.81UniSTS
SHGC-33423  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377105,909,871 - 105,909,971UniSTSGRCh37
Build 367105,697,107 - 105,697,207RGDNCBI36
Celera7100,715,398 - 100,715,498RGD
Cytogenetic Map7q22.3UniSTS
HuRef7100,269,485 - 100,269,585UniSTS
CRA_TCAGchr7v27105,270,875 - 105,270,975UniSTS
TNG Radiation Hybrid Map746152.0UniSTS
Stanford-G3 RH Map75164.0UniSTS
NCBI RH Map71089.7UniSTS
GeneMap99-G3 RH Map75164.0UniSTS


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 3 171 168 6 2 2 4 6 5
Medium 2312 2673 1651 594 1747 436 4314 2010 2582 364 1241 1594 171 1198 2757 3
Low 123 147 75 29 36 29 37 185 1148 55 215 15 4 1 26 3 1
Below cutoff 3 2

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_005746 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047419699 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047419700 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054356984 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054356985 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AC007032 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AI299587 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK023341 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK292851 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK304085 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL832518 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC020691 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC072439 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC106046 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BI859562 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH236947 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471070 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068271 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CS463832 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CS545604 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  FB775574 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HD117879 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HH762803 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  L29050 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  U02020 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000222553   ⟹   ENSP00000222553
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7106,248,298 - 106,284,983 (-)Ensembl
RefSeq Acc Id: ENST00000354289   ⟹   ENSP00000346242
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7106,261,490 - 106,285,192 (-)Ensembl
RefSeq Acc Id: ENST00000393618
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7106,269,415 - 106,284,557 (-)Ensembl
RefSeq Acc Id: ENST00000417537   ⟹   ENSP00000390896
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7106,272,461 - 106,284,951 (-)Ensembl
RefSeq Acc Id: ENST00000424768   ⟹   ENSP00000390591
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7106,248,313 - 106,285,966 (-)Ensembl
RefSeq Acc Id: ENST00000441045
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7106,272,166 - 106,284,951 (-)Ensembl
RefSeq Acc Id: ENST00000463871
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7106,250,043 - 106,257,477 (-)Ensembl
RefSeq Acc Id: ENST00000467730
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7106,268,335 - 106,269,205 (-)Ensembl
RefSeq Acc Id: ENST00000484527
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7106,259,928 - 106,277,161 (-)Ensembl
RefSeq Acc Id: ENST00000486949
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7106,271,095 - 106,275,226 (-)Ensembl
RefSeq Acc Id: ENST00000489358
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7106,272,039 - 106,284,950 (-)Ensembl
RefSeq Acc Id: ENST00000489732
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7106,250,043 - 106,284,994 (-)Ensembl
RefSeq Acc Id: ENST00000491027
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7106,263,150 - 106,284,951 (-)Ensembl
RefSeq Acc Id: ENST00000679461
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7106,250,048 - 106,271,979 (-)Ensembl
RefSeq Acc Id: ENST00000679643   ⟹   ENSP00000504962
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7106,248,710 - 106,284,983 (-)Ensembl
RefSeq Acc Id: ENST00000679717
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7106,259,897 - 106,284,983 (-)Ensembl
RefSeq Acc Id: ENST00000679873   ⟹   ENSP00000506282
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7106,248,368 - 106,285,009 (-)Ensembl
RefSeq Acc Id: ENST00000679894
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7106,250,043 - 106,273,139 (-)Ensembl
RefSeq Acc Id: ENST00000679951   ⟹   ENSP00000505427
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7106,250,043 - 106,284,973 (-)Ensembl
RefSeq Acc Id: ENST00000680077   ⟹   ENSP00000506239
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7106,248,298 - 106,284,951 (-)Ensembl
RefSeq Acc Id: ENST00000680129   ⟹   ENSP00000504872
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7106,250,701 - 106,284,997 (-)Ensembl
RefSeq Acc Id: ENST00000680152   ⟹   ENSP00000505353
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7106,250,552 - 106,284,951 (-)Ensembl
RefSeq Acc Id: ENST00000680468   ⟹   ENSP00000505172
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7106,250,043 - 106,284,934 (-)Ensembl
RefSeq Acc Id: ENST00000680482
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7106,250,043 - 106,259,287 (-)Ensembl
RefSeq Acc Id: ENST00000680516
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7106,259,905 - 106,270,322 (-)Ensembl
RefSeq Acc Id: ENST00000680584   ⟹   ENSP00000505012
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7106,248,309 - 106,285,094 (-)Ensembl
RefSeq Acc Id: ENST00000680616
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7106,250,552 - 106,257,483 (-)Ensembl
RefSeq Acc Id: ENST00000680669
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7106,248,309 - 106,284,971 (-)Ensembl
RefSeq Acc Id: ENST00000680675   ⟹   ENSP00000506337
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7106,248,298 - 106,284,935 (-)Ensembl
RefSeq Acc Id: ENST00000680708   ⟹   ENSP00000506527
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7106,248,298 - 106,284,983 (-)Ensembl
RefSeq Acc Id: ENST00000680786   ⟹   ENSP00000505453
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7106,250,745 - 106,284,555 (-)Ensembl
RefSeq Acc Id: ENST00000680823   ⟹   ENSP00000506618
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7106,250,043 - 106,284,973 (-)Ensembl
RefSeq Acc Id: ENST00000680864   ⟹   ENSP00000505845
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7106,248,308 - 106,285,000 (-)Ensembl
RefSeq Acc Id: ENST00000680991   ⟹   ENSP00000506283
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7106,248,298 - 106,284,983 (-)Ensembl
RefSeq Acc Id: ENST00000681223   ⟹   ENSP00000505065
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7106,250,836 - 106,284,992 (-)Ensembl
RefSeq Acc Id: ENST00000681255   ⟹   ENSP00000506129
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7106,248,332 - 106,285,966 (-)Ensembl
RefSeq Acc Id: ENST00000681297
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7106,263,150 - 106,271,979 (-)Ensembl
RefSeq Acc Id: ENST00000681372
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7106,250,053 - 106,267,826 (-)Ensembl
RefSeq Acc Id: ENST00000681391   ⟹   ENSP00000505390
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7106,248,298 - 106,284,983 (-)Ensembl
RefSeq Acc Id: ENST00000681455
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7106,252,514 - 106,254,876 (-)Ensembl
RefSeq Acc Id: ENST00000681456   ⟹   ENSP00000505633
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7106,248,298 - 106,284,951 (-)Ensembl
RefSeq Acc Id: ENST00000681491   ⟹   ENSP00000506540
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7106,248,298 - 106,285,436 (-)Ensembl
RefSeq Acc Id: ENST00000681494   ⟹   ENSP00000506450
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7106,248,298 - 106,284,983 (-)Ensembl
RefSeq Acc Id: ENST00000681550   ⟹   ENSP00000505112
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7106,248,298 - 106,284,632 (-)Ensembl
RefSeq Acc Id: ENST00000681631
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7106,259,879 - 106,265,590 (-)Ensembl
RefSeq Acc Id: ENST00000681653   ⟹   ENSP00000506565
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7106,248,298 - 106,284,983 (-)Ensembl
RefSeq Acc Id: ENST00000681878   ⟹   ENSP00000505577
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7106,250,039 - 106,284,971 (-)Ensembl
RefSeq Acc Id: ENST00000681887
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7106,250,672 - 106,284,686 (-)Ensembl
RefSeq Acc Id: ENST00000681936   ⟹   ENSP00000504973
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7106,250,431 - 106,284,544 (-)Ensembl
RefSeq Acc Id: NM_005746   ⟹   NP_005737
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387106,248,298 - 106,284,983 (-)NCBI
GRCh377105,888,731 - 105,926,373 (-)NCBI
Build 367105,675,967 - 105,712,874 (-)NCBI Archive
HuRef7100,248,062 - 100,285,253 (-)ENTREZGENE
CHM1_17105,822,212 - 105,859,137 (-)NCBI
T2T-CHM13v2.07107,563,712 - 107,600,408 (-)NCBI
CRA_TCAGchr7v27105,249,752 - 105,286,646 (-)ENTREZGENE
Sequence:
RefSeq Acc Id: XM_047419699   ⟹   XP_047275655
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387106,248,298 - 106,285,888 (-)NCBI
RefSeq Acc Id: XM_047419700   ⟹   XP_047275656
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387106,263,666 - 106,284,983 (-)NCBI
RefSeq Acc Id: XM_054356984   ⟹   XP_054212959
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.07107,563,712 - 107,602,631 (-)NCBI
RefSeq Acc Id: XM_054356985   ⟹   XP_054212960
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.07107,579,080 - 107,600,408 (-)NCBI
Protein Sequences
Protein RefSeqs NP_005737 (Get FASTA)   NCBI Sequence Viewer  
  XP_047275655 (Get FASTA)   NCBI Sequence Viewer  
  XP_047275656 (Get FASTA)   NCBI Sequence Viewer  
  XP_054212959 (Get FASTA)   NCBI Sequence Viewer  
  XP_054212960 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAA17884 (Get FASTA)   NCBI Sequence Viewer  
  AAF19249 (Get FASTA)   NCBI Sequence Viewer  
  AAH72439 (Get FASTA)   NCBI Sequence Viewer  
  AAI06047 (Get FASTA)   NCBI Sequence Viewer  
  AAQ96862 (Get FASTA)   NCBI Sequence Viewer  
  BAF85540 (Get FASTA)   NCBI Sequence Viewer  
  BAH14102 (Get FASTA)   NCBI Sequence Viewer  
  CAH56351 (Get FASTA)   NCBI Sequence Viewer  
  CAM12699 (Get FASTA)   NCBI Sequence Viewer  
  CAN36300 (Get FASTA)   NCBI Sequence Viewer  
  CAV30744 (Get FASTA)   NCBI Sequence Viewer  
  CBX74360 (Get FASTA)   NCBI Sequence Viewer  
  CBX78820 (Get FASTA)   NCBI Sequence Viewer  
  EAL24399 (Get FASTA)   NCBI Sequence Viewer  
  EAL24400 (Get FASTA)   NCBI Sequence Viewer  
  EAW83382 (Get FASTA)   NCBI Sequence Viewer  
  EAW83383 (Get FASTA)   NCBI Sequence Viewer  
  EAW83384 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000222553
  ENSP00000222553.3
  ENSP00000346242.4
  ENSP00000390591
  ENSP00000390591.2
  ENSP00000390896.2
  ENSP00000504872.1
  ENSP00000504962.1
  ENSP00000504973.1
  ENSP00000505012.1
  ENSP00000505065.1
  ENSP00000505112.1
  ENSP00000505172.1
  ENSP00000505245.1
  ENSP00000505320.1
  ENSP00000505353.1
  ENSP00000505390
  ENSP00000505390.1
  ENSP00000505427.1
  ENSP00000505453.1
  ENSP00000505577.1
  ENSP00000505633.1
  ENSP00000505845.1
  ENSP00000506129.1
  ENSP00000506239.1
  ENSP00000506282.1
  ENSP00000506283.1
  ENSP00000506337.1
  ENSP00000506343.1
  ENSP00000506450.1
  ENSP00000506527.1
  ENSP00000506540.1
  ENSP00000506565.1
  ENSP00000506618.1
GenBank Protein P43490 (Get FASTA)   NCBI Sequence Viewer  
Reference Protein Sequences
RefSeq Acc Id: NP_005737   ⟸   NM_005746
- Peptide Label: precursor
- UniProtKB: Q3KQV0 (UniProtKB/Swiss-Prot),   A4D0R0 (UniProtKB/Swiss-Prot),   A4D0Q9 (UniProtKB/Swiss-Prot),   Q8WW95 (UniProtKB/Swiss-Prot),   P43490 (UniProtKB/Swiss-Prot),   A0A7P0T895 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: ENSP00000390591   ⟸   ENST00000424768
RefSeq Acc Id: ENSP00000390896   ⟸   ENST00000417537
RefSeq Acc Id: ENSP00000346242   ⟸   ENST00000354289
RefSeq Acc Id: ENSP00000222553   ⟸   ENST00000222553
RefSeq Acc Id: ENSP00000506239   ⟸   ENST00000680077
RefSeq Acc Id: ENSP00000505172   ⟸   ENST00000680468
RefSeq Acc Id: ENSP00000506565   ⟸   ENST00000681653
RefSeq Acc Id: ENSP00000505633   ⟸   ENST00000681456
RefSeq Acc Id: ENSP00000506618   ⟸   ENST00000680823
RefSeq Acc Id: ENSP00000506283   ⟸   ENST00000680991
RefSeq Acc Id: ENSP00000505577   ⟸   ENST00000681878
RefSeq Acc Id: ENSP00000506129   ⟸   ENST00000681255
RefSeq Acc Id: ENSP00000504962   ⟸   ENST00000679643
RefSeq Acc Id: ENSP00000506540   ⟸   ENST00000681491
RefSeq Acc Id: ENSP00000506450   ⟸   ENST00000681494
RefSeq Acc Id: ENSP00000504872   ⟸   ENST00000680129
RefSeq Acc Id: ENSP00000505065   ⟸   ENST00000681223
RefSeq Acc Id: ENSP00000505427   ⟸   ENST00000679951
RefSeq Acc Id: ENSP00000505353   ⟸   ENST00000680152
RefSeq Acc Id: ENSP00000506282   ⟸   ENST00000679873
RefSeq Acc Id: ENSP00000505390   ⟸   ENST00000681391
RefSeq Acc Id: ENSP00000505453   ⟸   ENST00000680786
RefSeq Acc Id: ENSP00000505845   ⟸   ENST00000680864
RefSeq Acc Id: ENSP00000504973   ⟸   ENST00000681936
RefSeq Acc Id: ENSP00000505012   ⟸   ENST00000680584
RefSeq Acc Id: ENSP00000505112   ⟸   ENST00000681550
RefSeq Acc Id: ENSP00000506337   ⟸   ENST00000680675
RefSeq Acc Id: ENSP00000506527   ⟸   ENST00000680708
RefSeq Acc Id: XP_047275655   ⟸   XM_047419699
- Peptide Label: isoform X1
- UniProtKB: Q3KQV0 (UniProtKB/Swiss-Prot),   P43490 (UniProtKB/Swiss-Prot),   A4D0R0 (UniProtKB/Swiss-Prot),   A4D0Q9 (UniProtKB/Swiss-Prot),   Q8WW95 (UniProtKB/Swiss-Prot),   A0A7P0T895 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047275656   ⟸   XM_047419700
- Peptide Label: isoform X2
- UniProtKB: A0A7P0T941 (UniProtKB/TrEMBL),   A0A7P0Z466 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054212959   ⟸   XM_054356984
- Peptide Label: isoform X1
- UniProtKB: Q3KQV0 (UniProtKB/Swiss-Prot),   P43490 (UniProtKB/Swiss-Prot),   A4D0R0 (UniProtKB/Swiss-Prot),   A4D0Q9 (UniProtKB/Swiss-Prot),   Q8WW95 (UniProtKB/Swiss-Prot),   A0A7P0T895 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054212960   ⟸   XM_054356985
- Peptide Label: isoform X2
- UniProtKB: A0A7P0T941 (UniProtKB/TrEMBL),   A0A7P0Z466 (UniProtKB/TrEMBL)
Protein Domains
Nicotinamide phosphoribosyltransferase N-terminal   Nicotinate/nicotinamide phosphoribosyltransferase

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-P43490-F1-model_v2 AlphaFold P43490 1-491 view protein structure

Promoters
RGD ID:6805946
Promoter ID:HG_KWN:59199
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   Lymphoblastoid
Transcripts:OTTHUMT00000316773
Position:
Human AssemblyChrPosition (strand)Source
Build 367105,681,176 - 105,682,127 (-)MPROMDB
RGD ID:6805945
Promoter ID:HG_KWN:59200
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   HeLa_S3,   Lymphoblastoid
Transcripts:OTTHUMT00000316772
Position:
Human AssemblyChrPosition (strand)Source
Build 367105,697,206 - 105,697,706 (-)MPROMDB
RGD ID:6805506
Promoter ID:HG_KWN:59201
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   CD4+TCell_2Hour,   HeLa_S3,   Jurkat,   K562,   Lymphoblastoid,   NB4
Transcripts:ENST00000393617,   ENST00000393618,   OTTHUMT00000277146,   OTTHUMT00000316767,   OTTHUMT00000316768,   OTTHUMT00000316769,   OTTHUMT00000316770,   OTTHUMT00000316771,   OTTHUMT00000316776,   UC003VDR.1
Position:
Human AssemblyChrPosition (strand)Source
Build 367105,712,066 - 105,713,942 (-)MPROMDB
RGD ID:6851342
Promoter ID:EP73469
Type:multiple initiation site
Name:HS_PBEF
Description:Pre-B-cell colony-enhancing factor.
SO ACC ID:SO:0000170
Source:EPD (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:NEDO full length human cDNA sequencing project.; Oligo-capping
Position:
Human AssemblyChrPosition (strand)Source
Build 367105,712,633 - 105,712,693EPD
RGD ID:7211605
Promoter ID:EPDNEW_H11548
Type:initiation region
Name:NAMPT_1
Description:nicotinamide phosphoribosyltransferase
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H11549  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh387106,284,983 - 106,285,043EPDNEW
RGD ID:7211607
Promoter ID:EPDNEW_H11549
Type:initiation region
Name:NAMPT_2
Description:nicotinamide phosphoribosyltransferase
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H11548  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh387106,285,118 - 106,285,178EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:30092 AgrOrtholog
COSMIC NAMPT COSMIC
Ensembl Genes ENSG00000105835 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000222553 ENTREZGENE
  ENST00000222553.8 UniProtKB/Swiss-Prot
  ENST00000354289.9 UniProtKB/TrEMBL
  ENST00000417537.2 UniProtKB/TrEMBL
  ENST00000424768 ENTREZGENE, UniProtKB/TrEMBL
  ENST00000424768.2 UniProtKB/Swiss-Prot
  ENST00000441045.6 UniProtKB/TrEMBL
  ENST00000489358.5 UniProtKB/TrEMBL
  ENST00000491027.6 UniProtKB/TrEMBL
  ENST00000679643.1 UniProtKB/TrEMBL
  ENST00000679873.1 UniProtKB/TrEMBL
  ENST00000679951.1 UniProtKB/TrEMBL
  ENST00000680077.1 UniProtKB/TrEMBL
  ENST00000680129.1 UniProtKB/TrEMBL
  ENST00000680152.1 UniProtKB/TrEMBL
  ENST00000680468.1 UniProtKB/TrEMBL
  ENST00000680584.1 UniProtKB/TrEMBL
  ENST00000680675.1 UniProtKB/TrEMBL
  ENST00000680708.1 UniProtKB/TrEMBL
  ENST00000680786.1 UniProtKB/TrEMBL
  ENST00000680823.1 UniProtKB/TrEMBL
  ENST00000680864.1 UniProtKB/TrEMBL
  ENST00000680991.1 UniProtKB/TrEMBL
  ENST00000681223.1 UniProtKB/TrEMBL
  ENST00000681255.1 UniProtKB/Swiss-Prot
  ENST00000681391 ENTREZGENE
  ENST00000681391.1 UniProtKB/TrEMBL
  ENST00000681456.1 UniProtKB/TrEMBL
  ENST00000681491.1 UniProtKB/Swiss-Prot
  ENST00000681494.1 UniProtKB/TrEMBL
  ENST00000681550.1 UniProtKB/TrEMBL
  ENST00000681653.1 UniProtKB/TrEMBL
  ENST00000681878.1 UniProtKB/TrEMBL
  ENST00000681936.1 UniProtKB/TrEMBL
Gene3D-CATH 3.20.20.70 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000105835 GTEx
HGNC ID HGNC:30092 ENTREZGENE
Human Proteome Map NAMPT Human Proteome Map
InterPro Aldolase_TIM UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  DUF5598 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  N/Namide_PRibTrfase UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Nicotinamide_PRibTrfase UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Nicotinate_pribotase-like_C UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:10135 UniProtKB/Swiss-Prot
NCBI Gene 10135 ENTREZGENE
OMIM 608764 OMIM
PANTHER NICOTINAMIDE PHOSPHORIBOSYLTRANSFERASE UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PTHR43816 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam DUF5598 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  NAPRTase UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB NAMPT RGD, PharmGKB
PIRSF NMPRT UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP Nicotinate/Quinolinate PRTase N-terminal domain-like UniProtKB/TrEMBL
  SSF51690 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A0C4DFS8_HUMAN UniProtKB/TrEMBL
  A0A7P0T862_HUMAN UniProtKB/TrEMBL
  A0A7P0T895 ENTREZGENE, UniProtKB/TrEMBL
  A0A7P0T8D2_HUMAN UniProtKB/TrEMBL
  A0A7P0T8L3_HUMAN UniProtKB/TrEMBL
  A0A7P0T8R4_HUMAN UniProtKB/TrEMBL
  A0A7P0T8Z3_HUMAN UniProtKB/TrEMBL
  A0A7P0T931_HUMAN UniProtKB/TrEMBL
  A0A7P0T941 ENTREZGENE, UniProtKB/TrEMBL
  A0A7P0T973_HUMAN UniProtKB/TrEMBL
  A0A7P0T9F0_HUMAN UniProtKB/TrEMBL
  A0A7P0T9I9_HUMAN UniProtKB/TrEMBL
  A0A7P0TA73_HUMAN UniProtKB/TrEMBL
  A0A7P0TAI8_HUMAN UniProtKB/TrEMBL
  A0A7P0TAS5_HUMAN UniProtKB/TrEMBL
  A0A7P0TAZ2_HUMAN UniProtKB/TrEMBL
  A0A7P0TB17_HUMAN UniProtKB/TrEMBL
  A0A7P0TBB7_HUMAN UniProtKB/TrEMBL
  A0A7P0Z437_HUMAN UniProtKB/TrEMBL
  A0A7P0Z466 ENTREZGENE, UniProtKB/TrEMBL
  A0A7P0Z4L4_HUMAN UniProtKB/TrEMBL
  A0A7P0Z4N0_HUMAN UniProtKB/TrEMBL
  A4D0Q9 ENTREZGENE
  A4D0R0 ENTREZGENE
  B7Z8W6_HUMAN UniProtKB/TrEMBL
  C9JF35_HUMAN UniProtKB/TrEMBL
  C9JG65_HUMAN UniProtKB/TrEMBL
  NAMPT_HUMAN UniProtKB/Swiss-Prot, ENTREZGENE
  Q3KQV0 ENTREZGENE
  Q8WW95 ENTREZGENE
UniProt Secondary A4D0Q9 UniProtKB/Swiss-Prot
  A4D0R0 UniProtKB/Swiss-Prot
  Q3KQV0 UniProtKB/Swiss-Prot
  Q8WW95 UniProtKB/Swiss-Prot