NAPRT

Nicotinate phosphoribosyltransferase Q6XQN6 PNCB_HUMAN
Protein Coding Chr 8 8q24.3 Swiss-Prot reviewed Entrez 93100
Mutations
582
CL 106 · Tissue 474
Samples
216
CL 63 · Tissue 151
Peptides
175
unique mutant peptides
Transcripts
4
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
Mutations582106474
Samples21663151
Peptides17537141

Function

NAPRT · Nicotinate phosphoribosyltransferase

Nicotinic acid (NA; niacin) is converted by nicotinic acid phosphoribosyltransferase (NAPRT; EC 2.4.2.11) to NA mononucleotide (NaMN), which is then converted to NA adenine dinucleotide (NaAD), and finally to nicotinamide adenine dinucleotide (NAD), which serves as a coenzyme in cellular redox reactions and is an essential component of a variety of processes in cellular metabolism including response to stress (Hara et al., 2007).[supplied by OMIM, Mar 2008].

Isoforms & Proteins

4 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
ENST00000449291 Q6XQN6 230 166
ENST00000426292 Q6XQN6-3 178 143
ENST00000435154 C9J8U2* 173 140
ENST00000460623 A0A087WUT5* 1 1

Gene Properties

Type
Protein Coding
Chromosome
8
Cytoband
8q24.3
Entrez ID
Aliases
NAPRT1PP3856

Recurrent Mutations

All 166 amino-acid changes on canonical ENST00000449291 · 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 NAPRT · 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 NAPRT – 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
Chronic Myelogenous Leukemia
1/25 4%
0/0 0%
Acute Monocytic Leukemia
0/1 0%
1/25 4%
Acute Myeloid Leukemia
3/90 3%
0/0 0%
T-Lymphoblastic Leukemia
1/40 2%
0/0 0%
Hodgkins Lymphoma
1/16 6%
1/122 1%
Non-Small Cell Lung Carcinoma
11/304 4%
8/1390 1%
Endometrial Carcinoma
2/42 5%
5/612 1%
Glioblastoma
1/98 1%
0/0 0%
Thyroid Gland Carcinoma
1/45 2%
15/1592 1%
Colorectal Carcinoma
9/143 6%
22/3239 1%
Melanoma
4/210 2%
15/1899 1%
Burkitts Lymphoma
2/32 6%
0/196 0%
Bladder Carcinoma
0/58 0%
8/956 1%
Gastric Carcinoma
3/74 4%
10/1809 1%
Other Sarcomas
2/69 3%
3/699 0%
Ewings Sarcoma
2/63 3%
0/262 0%
Head and Neck Carcinoma
1/85 1%
9/1574 1%
Biliary Tract Carcinoma
3/54 6%
3/950 0%
Osteosarcoma
1/45 2%
0/166 0%
Mesothelioma
1/62 2%
0/165 0%
Other Solid Cancers
0/94 0%
6/1515 0%
Ovarian Carcinoma
2/109 2%
2/998 0%
Squamous Cell Lung Carcinoma
1/57 2%
2/810 0%
Non-Cancerous
1/104 1%
2/830 0%
Glioma
0/52 0%
7/2127 0%
Kidney Carcinoma
0/85 0%
6/1862 0%
Plasma Cell Myeloma
0/44 0%
1/305 0%
Neuroendocrine Tumour
0/154 0%
2/577 0%
B-Cell Non-Hodgkins Lymphoma
2/88 2%
4/2534 0%
Cervical Carcinoma
1/35 3%
0/422 0%

Mutation Distribution

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

Mutation counts by tissue
Mutation Distribution

How many mutations in NAPRT 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 582 mutations in NAPRT

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