CENPE

Centromere protein E Q02224 CENPE_HUMAN
Protein Coding Chr 4 4q24 Swiss-Prot reviewed Entrez 1062
Mutations
2,090
CL 318 · Tissue 1,751
Samples
955
CL 182 · Tissue 765
Peptides
873
unique mutant peptides
Transcripts
2
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
Mutations2,0903181,751
Samples955182765
Peptides873135737

Function

CENPE · Centromere protein E

Centrosome-associated protein E (CENPE) is a kinesin-like motor protein that accumulates in the G2 phase of the cell cycle. Unlike other centrosome-associated proteins, it is not present during interphase and first appears at the centromere region of chromosomes during prometaphase. This protein is required for stable spindle microtubule capture at kinetochores which is a necessary step in chromosome alignment during prometaphase. This protein also couples chromosome position to microtubule depolymerizing activity. Alternative splicing results in multiple transcript variants encoding distinct protein isoforms. [provided by RefSeq, Nov 2014].

Isoforms & Proteins

2 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
ENST00000265148 Q02224 1,132 854
ENST00000380026 Q02224-3 958 764

Gene Properties

Type
Protein Coding
Chromosome
4
Cytoband
4q24
Entrez ID
Aliases
CENP-EKIF10MCPH13PPP1R61

Recurrent Mutations

All 854 amino-acid changes on canonical ENST00000265148 · 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 CENPE · 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 CENPE – 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
Endometrial Carcinoma
13/42 31%
42/612 7%
Glioblastoma
8/98 8%
0/0 0%
Acute Myeloid Leukemia
6/90 7%
0/0 0%
Melanoma
15/210 7%
109/1899 6%
Non-Small Cell Lung Carcinoma
19/304 6%
60/1390 4%
Squamous Cell Lung Carcinoma
4/57 7%
32/810 4%
Chronic Myelogenous Leukemia
1/25 4%
0/0 0%
T-Cell Non-Hodgkins Lymphoma
1/26 4%
0/0 0%
Gastrointestinal Stromal Tumour
0/0 0%
5/133 4%
Bladder Carcinoma
6/58 10%
30/956 3%
Colorectal Carcinoma
23/143 16%
87/3239 3%
Cervical Carcinoma
0/35 0%
14/422 3%
Unknown
0/10 0%
1/29 3%
T-Lymphoblastic Leukemia
1/40 2%
0/0 0%
Other Solid Cancers
6/94 6%
29/1515 2%
Small Cell Lung Carcinoma
2/9 22%
14/752 2%
Other Sarcomas
4/69 6%
10/699 1%
Thyroid Gland Carcinoma
0/45 0%
29/1592 2%
Gastric Carcinoma
6/74 8%
27/1809 1%
Esophageal Squamous Cell Carcinoma
0/51 0%
45/2550 2%
Breast Carcinoma
14/144 10%
45/3264 1%
Plasma Cell Myeloma
4/44 9%
2/305 1%
Head and Neck Carcinoma
2/85 2%
24/1574 2%
Neuroendocrine Tumour
5/154 3%
6/577 1%
Rhabdomyosarcoma
1/33 3%
2/171 1%
Hepatocellular Carcinoma
1/46 2%
31/2210 1%
Esophageal Carcinoma
0/23 0%
11/769 1%
Burkitts Lymphoma
1/32 3%
2/196 1%
Mesothelioma
3/62 5%
0/165 0%
Ewings Sarcoma
3/63 5%
1/262 0%

Mutation Distribution

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

Mutation counts by tissue
Mutation Distribution

How many mutations in CENPE 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 2,090 mutations in CENPE

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