NAMPT nicotinamide phosphoribosyltransferase

Information
Symbol
NAMPT
Type
protein-coding
Description
nicotinamide phosphoribosyltransferase
Entrez Gene ID
10135
Genome
hg19
Position
chr7:105,888,759-105,926,412
Genome
hg38
Position
chr7:106,248,313-106,285,966
MIM
608764 OMIM
HGNC
HGNC:30092 HGNC
Ensembl
ENSG00000105835 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 8
Likely benign 0 4
Uncertain significance 0 16
Ranking
ClinVar
0
0
0
28
0
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
[No Data.]
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Variant name Gene AA change CDS Japanese
frequency		 TogoVar MGeND Genome ClinVar CIViC evidence DisGeNET entry COSMIC
occurrence		 Prediction
Entry Origin Type Annotation Entry Origin Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Size Chromosome Start Stop Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Gene symbol Chromosome Genomic start Genomic stop Strand Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
TypeID
SYNONYM 1110035O14Rik
SYNONYM PBEF
SYNONYM PBEF1
SYNONYM VF
SYNONYM VISFATIN
MIM 608764 OMIM
HGNC HGNC:30092 HGNC
Ensembl ENSG00000105835 Ensembl
AllianceGenome HGNC:30092
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000679643.1 hg38 chr7 106,248,710 106,284,983 36,274
ENST00000681255.1 hg38 chr7 106,248,332 106,285,966 37,635
ENST00000680468.1 hg38 chr7 106,250,043 106,284,934 34,892
ENST00000441045.6 hg38 chr7 106,272,166 106,284,951 12,786
ENST00000222553.8 hg38 chr7 106,248,298 106,284,983 36,686
ENST00000417537.2 hg38 chr7 106,272,461 106,284,951 12,491
ENST00000680823.1 hg38 chr7 106,250,043 106,284,973 34,931
ENST00000681550.1 hg38 chr7 106,248,298 106,284,632 36,335
ENST00000354289.9 hg38 chr7 106,261,490 106,285,192 23,703
ENST00000681491.1 hg38 chr7 106,248,298 106,285,436 37,139
ENST00000424768.2 hg38 chr7 106,248,313 106,285,966 37,654
ENST00000681936.1 hg38 chr7 106,250,431 106,284,544 34,114
ENST00000491027.6 hg38 chr7 106,263,150 106,284,951 21,802
ENST00000681878.1 hg38 chr7 106,250,039 106,284,971 34,933
ENST00000489358.5 hg38 chr7 106,272,039 106,284,950 12,912
ENST00000679951.1 hg38 chr7 106,250,043 106,284,973 34,931
ENST00000680786.1 hg38 chr7 106,250,745 106,284,555 33,811
ENST00000680584.1 hg38 chr7 106,248,309 106,285,094 36,786
ENST00000680468.1 hg19 chr7 105,890,489 105,925,380 34,892
ENST00000679951.1 hg19 chr7 105,890,489 105,925,419 34,931
ENST00000354289.9 hg19 chr7 105,901,936 105,925,638 23,703
ENST00000491027.6 hg19 chr7 105,903,596 105,925,397 21,802
ENST00000489358.5 hg19 chr7 105,912,485 105,925,396 12,912
ENST00000441045.6 hg19 chr7 105,912,612 105,925,397 12,786
ENST00000417537.2 hg19 chr7 105,912,907 105,925,397 12,491
ENST00000681550.1 hg19 chr7 105,888,744 105,925,078 36,335
ENST00000222553.8 hg19 chr7 105,888,744 105,925,429 36,686
ENST00000424768.2 hg19 chr7 105,888,759 105,926,412 37,654
ENST00000681491.1 hg19 chr7 105,888,744 105,925,882 37,139
ENST00000680584.1 hg19 chr7 105,888,755 105,925,540 36,786
ENST00000680786.1 hg19 chr7 105,891,191 105,925,001 33,811
ENST00000681255.1 hg19 chr7 105,888,778 105,926,412 37,635
ENST00000679643.1 hg19 chr7 105,889,156 105,925,429 36,274
ENST00000680823.1 hg19 chr7 105,890,489 105,925,419 34,931
ENST00000681936.1 hg19 chr7 105,890,877 105,924,990 34,114
ENST00000681878.1 hg19 chr7 105,890,485 105,925,417 34,933
Genome browser