NAMPT

Nicotinamide phosphoribosyltransferase P43490 NAMPT_HUMAN
Protein Coding Chr 7 7q22.3 Swiss-Prot reviewed Entrez 10135
Mutations
322
CL 82 · Tissue 232
Samples
188
CL 53 · Tissue 129
Peptides
153
unique mutant peptides
Transcripts
5
isoforms mutated

Stats by Source

Total, split by cell line (COSMIC CL / DepMap / PubMed) vs tissue (COSMIC primary tissue)

How the counts split by source
Stats by Source

Total = all mutations for this gene across every source.

Cell line = COSMIC Cell Lines Project + DepMap + PubMed.

Tissue = COSMIC primary-tissue (patient tumour) samples.

Total can exceed cell line + tissue: COSMIC tissue-derived models sit only in global, and a peptide can be shared across both.

TotalCell lineTissue
Mutations32282232
Samples18853129
Peptides15331119

Function

NAMPT · Nicotinamide phosphoribosyltransferase

This gene encodes a protein that catalyzes the condensation of nicotinamide with 5-phosphoribosyl-1-pyrophosphate to yield nicotinamide mononucleotide, one step in the biosynthesis of nicotinamide adenine dinucleotide. The protein belongs to the nicotinic acid phosphoribosyltransferase (NAPRTase) family and is thought to be involved in many important biological processes, including metabolism, stress response and aging. This gene has a pseudogene on chromosome 10. [provided by RefSeq, Feb 2011].

Isoforms & Proteins

5 transcripts · UniProt mapping is sequence-verified (AA-safe)

About the isoform mapping
Isoforms & Proteins

Each Ensembl transcript (ENST) this gene is mutated on, with its matched UniProt accession.

The mapping is sequence-verified: the UniProt sequence is identical to the transcript translation, so amino-acid positions line up exactly. A * marks an unreviewed (TrEMBL) entry.

Counts are mutations and unique mutant peptides on each transcript.

TranscriptUniProtMutationsPeptides
ENST00000222553 P43490 192 145
ENST00000354289 A0A0C4DFS8* 126 103
ENST00000679643 A0A7P0T862* 2 1
ENST00000424768 P43490 1 1
ENST00000680077 A0A7P0TAI8* 1 1

Gene Properties

Type
Protein Coding
Chromosome
7
Cytoband
7q22.3
Entrez ID
Aliases
1110035O14RikPBEFPBEF1VFVISFATIN

Recurrent Mutations

All 145 amino-acid changes on canonical ENST00000222553 · needle height = samples · drag the mini-map to zoom

What this lollipop shows
Recurrent Mutations

A lollipop / needle plot – the standard way to show recurrent mutations along a protein (as used by cBioPortal and MutationMapper).

X-axis = amino-acid position in the protein.

Needle height & head size = how often that exact amino-acid change was observed (its recurrence). Tall/large heads are mutational hotspots.

The most recurrent changes are labelled; hover any needle for the change, position and counts.

Mutation frequency across cancer types

% of samples with a missense/complex mutation in NAMPT · cell line vs tissue

How this frequency is counted
Cancer-type mutation frequency

For each cancer type, the fraction of samples that carry at least one missense/complex mutation anywhere in NAMPT – counted as distinct samples (a sample counts once no matter how many mutations it has).

Split into cell line and tissue; each cell shows mutated / total and the percentage. Cohorts with <20 samples are omitted. Ordered by combined frequency.

Cancer typeCell linesTissue samples
Oral Cavity Carcinoma
2/54 4%
0/0 0%
T-Lymphoblastic Leukemia
1/40 2%
0/0 0%
Endometrial Carcinoma
2/42 5%
10/612 2%
Non-Small Cell Lung Carcinoma
9/304 3%
10/1390 1%
Acute Myeloid Leukemia
1/90 1%
0/0 0%
Germ Cell Tumour
0/25 0%
2/169 1%
Colorectal Carcinoma
13/143 9%
14/3239 0%
Melanoma
6/210 3%
10/1899 1%
Other Solid Cancers
0/94 0%
12/1515 1%
Neuroendocrine Tumour
3/154 2%
2/577 0%
Esophageal Carcinoma
0/23 0%
5/769 1%
Esophageal Squamous Cell Carcinoma
0/51 0%
14/2550 1%
Ovarian Carcinoma
3/109 3%
3/998 0%
Biliary Tract Carcinoma
1/54 2%
4/950 0%
Rhabdomyosarcoma
1/33 3%
0/171 0%
Bladder Carcinoma
0/58 0%
5/956 1%
Squamous Cell Lung Carcinoma
0/57 0%
4/810 0%
Cervical Carcinoma
2/35 6%
0/422 0%
Burkitts Lymphoma
1/32 3%
0/196 0%
Gastric Carcinoma
1/74 1%
7/1809 0%
Small Cell Lung Carcinoma
0/9 0%
3/752 0%
Ewings Sarcoma
0/63 0%
1/262 0%
Glioma
0/52 0%
6/2127 0%
Breast Carcinoma
3/144 2%
6/3264 0%
Other Sarcomas
2/69 3%
0/699 0%
Medulloblastoma
0/0 0%
1/450 0%
Kidney Carcinoma
0/85 0%
4/1862 0%
Head and Neck Carcinoma
0/85 0%
3/1574 0%
Hepatocellular Carcinoma
0/46 0%
4/2210 0%
B-Cell Non-Hodgkins Lymphoma
2/88 2%
2/2534 0%

Mutation Distribution

Where NAMPT is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in NAMPT were found in each tissue, across the whole database.

Each bar is a tissue (cell-line and tissue names are merged to the standard tissue), split into cell line and tissue (patient tumour) contributions.

This shows the cancer-context where this gene is recurrently altered.

GTEx Expression

Median TPM across 54 healthy tissues

GTEx Portal ↗
About the expression data
GTEx Expression

Median gene expression (TPM) in normal, non-cancer human tissues from the GTEx project.

Useful for judging tumour specificity – a strong neoantigen target ideally comes from a gene with low expression in healthy tissues.

Scroll or drag the mini-axis below the chart to browse all tissues.

Mutations

All 322 mutations in NAMPT

About the mutation list
Mutations

Every mutation record for this gene, across all samples and sources.

The Sample column links to the cell line (cell-line samples) or the tissue type (tissue samples).

Use the Type / Source filters, the search box, and column sorting to explore; each CAN-IMMUNE ID opens the full mutation & peptide view.

IDSampleTranscriptAA Change CDSTypeSourceMutant PeptideWild-type Peptide