TJP1

Tight junction protein 1 Q07157 ZO1_HUMAN
Protein Coding Chr 15 15q13.1 Swiss-Prot reviewed Entrez 7082
Mutations
3,151
CL 453 · Tissue 2,675
Samples
748
CL 163 · Tissue 576
Peptides
730
unique mutant peptides
Transcripts
7
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
Mutations3,1514532,675
Samples748163576
Peptides730136608

Function

TJP1 · Tight junction protein 1

This gene encodes a member of the membrane-associated guanylate kinase (MAGUK) family of proteins, and acts as a tight junction adaptor protein that also regulates adherens junctions. Tight junctions regulate the movement of ions and macromolecules between endothelial and epithelial cells. The multidomain structure of this scaffold protein, including a postsynaptic density 95/disc-large/zona occludens (PDZ) domain, a Src homology (SH3) domain, a guanylate kinase (GuK) domain and unique (U) motifs all help to co-ordinate binding of transmembrane proteins, cytosolic proteins, and F-actin, which are required for tight junction function. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Aug 2017].

Isoforms & Proteins

7 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
ENST00000346128 Q07157 731 568
ENST00000545208 Q07157-2 716 555
ENST00000400011 G5E9E7* 703 544
ENST00000621049 A0A087X0K9* 674 521
ENST00000495972 H0YKB1* 131 105
ENST00000614355 A0A087X0K9* 131 117
ENST00000356107 G3V1L9* 65 52

Gene Properties

Type
Protein Coding
Chromosome
15
Cytoband
15q13.1
Entrez ID
Aliases
ZO-1

Recurrent Mutations

All 568 amino-acid changes on canonical ENST00000346128 · 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 TJP1 · 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 TJP1 – 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
8/40 20%
0/0 0%
T-Cell Non-Hodgkins Lymphoma
4/26 15%
0/0 0%
Endometrial Carcinoma
8/42 19%
37/612 6%
Oral Cavity Carcinoma
3/54 6%
0/0 0%
Acute Myeloid Leukemia
4/90 4%
0/0 0%
Chronic Myelogenous Leukemia
1/25 4%
0/0 0%
Squamous Cell Lung Carcinoma
4/57 7%
29/810 4%
Rhabdomyosarcoma
3/33 9%
4/171 2%
Melanoma
8/210 4%
59/1899 3%
Other Solid Cancers
7/94 7%
43/1515 3%
Colorectal Carcinoma
21/143 15%
84/3239 3%
Cervical Carcinoma
3/35 9%
10/422 2%
Burkitts Lymphoma
6/32 19%
0/196 0%
Gastric Carcinoma
1/74 1%
48/1809 3%
Plasma Cell Myeloma
5/44 11%
4/305 1%
Unknown
1/10 10%
0/29 0%
Non-Small Cell Lung Carcinoma
7/304 2%
24/1390 2%
Small Cell Lung Carcinoma
1/9 11%
11/752 1%
Other Sarcomas
4/69 6%
8/699 1%
Neuroendocrine Tumour
10/154 6%
1/577 0%
Hodgkins Lymphoma
1/16 6%
1/122 1%
Ewings Sarcoma
2/63 3%
2/262 1%
Esophageal Carcinoma
0/23 0%
9/769 1%
Bladder Carcinoma
2/58 3%
9/956 1%
Head and Neck Carcinoma
4/85 5%
14/1574 1%
Ovarian Carcinoma
4/109 4%
8/998 1%
Non-Cancerous
0/104 0%
10/830 1%
Thyroid Gland Carcinoma
0/45 0%
17/1592 1%
Glioblastoma
1/98 1%
0/0 0%
Biliary Tract Carcinoma
1/54 2%
9/950 1%

Mutation Distribution

Where TJP1 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in TJP1 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 3,151 mutations in TJP1

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