NXPE3

Neurexophilin and PC-esterase domain family member 3 Q969Y0 NXPE3_HUMAN
Protein Coding Chr 3 3q12.3 Swiss-Prot reviewed Entrez 91775
Mutations
802
CL 84 · Tissue 696
Samples
267
CL 40 · Tissue 220
Peptides
210
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
Mutations80284696
Samples26740220
Peptides21030178

Function

NXPE3 · Neurexophilin and PC-esterase domain family member 3

This gene encodes a member of the neurexophilin family of neuropeptide-like glycoproteins. The encoded protein contains a variable N-terminal domain, a highly conserved neurexophilin and PC-esterase (NXPE) central domain, a short linker region, and a cysteine-rich C-terminal domain. This protein binds alpha neurexins, a group of presynaptic transmembrane receptors that promote adhesion between dendrites and axons. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2017].

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
ENST00000273347 Q969Y0 280 208
ENST00000477909 Q969Y0 260 197
ENST00000491511 Q969Y0 260 197
ENST00000704528 A0A994J739* 2 2

Gene Properties

Type
Protein Coding
Chromosome
3
Cytoband
3q12.3
Entrez ID
Aliases
FAM55CMST115MSTP115

Recurrent Mutations

All 208 amino-acid changes on canonical ENST00000273347 · 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 NXPE3 · 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 NXPE3 – 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
T-Cell Non-Hodgkins Lymphoma
1/26 4%
0/0 0%
Endometrial Carcinoma
3/42 7%
14/612 2%
Melanoma
0/210 0%
37/1899 2%
Gastric Carcinoma
1/74 1%
23/1809 1%
Acute Myeloid Leukemia
1/90 1%
0/0 0%
Colorectal Carcinoma
5/143 4%
32/3239 1%
Non-Small Cell Lung Carcinoma
8/304 3%
10/1390 1%
Glioblastoma
1/98 1%
0/0 0%
Hepatocellular Carcinoma
3/46 7%
16/2210 1%
Squamous Cell Lung Carcinoma
2/57 4%
5/810 1%
Other Solid Cancers
0/94 0%
12/1515 1%
Gastrointestinal Stromal Tumour
0/0 0%
1/133 1%
Hodgkins Lymphoma
0/16 0%
1/122 1%
Bladder Carcinoma
0/58 0%
6/956 1%
Ovarian Carcinoma
2/109 2%
4/998 0%
Small Cell Lung Carcinoma
0/9 0%
4/752 1%
Germ Cell Tumour
0/25 0%
1/169 1%
Rhabdomyosarcoma
1/33 3%
0/171 0%
Glioma
1/52 2%
9/2127 0%
Cervical Carcinoma
0/35 0%
2/422 0%
Pancreatic Carcinoma
4/89 4%
2/1611 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
9/2550 0%
Breast Carcinoma
2/144 1%
9/3264 0%
Kidney Carcinoma
0/85 0%
6/1862 0%
Head and Neck Carcinoma
0/85 0%
5/1574 0%
Biliary Tract Carcinoma
0/54 0%
3/950 0%
Plasma Cell Myeloma
0/44 0%
1/305 0%
Neuroendocrine Tumour
2/154 1%
0/577 0%
Other Sarcomas
0/69 0%
2/699 0%
Esophageal Carcinoma
0/23 0%
2/769 0%

Mutation Distribution

Where NXPE3 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in NXPE3 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 802 mutations in NXPE3

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