CENPJ

CENPJ protein Q9HC77 CPAP_HUMAN
Swiss-Prot reviewed
Mutations
1,624
CL 361 · Tissue 1,248
Samples
594
CL 152 · Tissue 434
Peptides
460
unique mutant peptides
Transcripts
3
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
Mutations1,6243611,248
Samples594152434
Peptides46070394

Isoforms & Proteins

3 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
ENST00000381884 Q9HC77 654 444
ENST00000545981 F6VUX8* 489 346
ENST00000616936 Q9HC77-2 481 338

Gene Properties

Recurrent Mutations

All 444 amino-acid changes on canonical ENST00000381884 · 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 CENPJ · 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 CENPJ – 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-Lymphoblastic Leukemia
5/40 12%
0/0 0%
Chronic Myelogenous Leukemia
2/25 8%
0/0 0%
Oral Cavity Carcinoma
4/54 7%
0/0 0%
Endometrial Carcinoma
7/42 17%
25/612 4%
Acute Myeloid Leukemia
3/90 3%
0/0 0%
Squamous Cell Lung Carcinoma
6/57 11%
21/810 3%
Colorectal Carcinoma
15/143 10%
70/3239 2%
Gastric Carcinoma
9/74 12%
35/1809 2%
Melanoma
6/210 3%
43/1899 2%
Non-Small Cell Lung Carcinoma
14/304 5%
22/1390 2%
Glioblastoma
2/98 2%
0/0 0%
Cervical Carcinoma
3/35 9%
6/422 1%
Bladder Carcinoma
1/58 2%
19/956 2%
Osteosarcoma
3/45 7%
1/166 1%
Retinoblastoma
1/27 4%
0/30 0%
Other Solid Cancers
3/94 3%
24/1515 2%
Ewings Sarcoma
3/63 5%
2/262 1%
Gastrointestinal Stromal Tumour
0/0 0%
2/133 2%
Other Sarcomas
0/69 0%
11/699 2%
Esophageal Carcinoma
1/23 4%
10/769 1%
Thyroid Gland Carcinoma
7/45 16%
13/1592 1%
Hepatocellular Carcinoma
7/46 15%
20/2210 1%
Plasma Cell Myeloma
2/44 5%
2/305 1%
Neuroendocrine Tumour
4/154 3%
4/577 1%
Ovarian Carcinoma
4/109 4%
8/998 1%
Germ Cell Tumour
1/25 4%
1/169 1%
Head and Neck Carcinoma
5/85 6%
12/1574 1%
Small Cell Lung Carcinoma
0/9 0%
7/752 1%
Adrenocortical Carcinoma
0/3 0%
1/112 1%
Non-Cancerous
0/104 0%
7/830 1%

Mutation Distribution

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

Mutation counts by tissue
Mutation Distribution

How many mutations in CENPJ 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 1,624 mutations in CENPJ

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