PATJ

PATJ crumbs cell polarity complex component Q8NI35 INADL_HUMAN
Protein Coding Chr 1 1p31.3 Swiss-Prot reviewed Entrez 10207
Mutations
2,723
CL 384 · Tissue 2,317
Samples
852
CL 175 · Tissue 669
Peptides
720
unique mutant peptides
Transcripts
5
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
Mutations2,7233842,317
Samples852175669
Peptides720124608

Function

PATJ · PATJ crumbs cell polarity complex component

This gene encodes a protein with multiple PDZ domains. PDZ domains mediate protein-protein interactions, and proteins with multiple PDZ domains often organize multimeric complexes at the plasma membrane. This protein localizes to tight junctions and to the apical membrane of epithelial cells. A similar protein in Drosophila is a scaffolding protein which tethers several members of a multimeric signaling complex in photoreceptors. [provided by RefSeq, Jul 2008].

Isoforms & Proteins

5 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
ENST00000642238 A0A2R8Y549* 960 678
ENST00000371158 Q8NI35 849 622
ENST00000646453 A0A2R8Y5I3* 340 252
ENST00000635137 A0A0U1RQT2* 322 236
ENST00000307297 A0ACM8QGA2* 252 178

Gene Properties

Type
Protein Coding
Chromosome
1
Cytoband
1p31.3
Entrez ID
Aliases
CippINADLInaD-likehINADL

Recurrent Mutations

All 622 amino-acid changes on canonical ENST00000371158 · 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 PATJ · 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 PATJ – 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%
Endometrial Carcinoma
8/42 19%
40/612 7%
Melanoma
11/210 5%
119/1899 6%
Oral Cavity Carcinoma
3/54 6%
0/0 0%
Unknown
1/10 10%
1/29 3%
Glioblastoma
4/98 4%
0/0 0%
Non-Small Cell Lung Carcinoma
20/304 7%
44/1390 3%
Cervical Carcinoma
3/35 9%
12/422 3%
Squamous Cell Lung Carcinoma
5/57 9%
21/810 3%
Colorectal Carcinoma
22/143 15%
77/3239 2%
Gastric Carcinoma
8/74 11%
42/1809 2%
Acute Myeloid Leukemia
2/90 2%
0/0 0%
Bladder Carcinoma
3/58 5%
19/956 2%
Other Solid Cancers
7/94 7%
26/1515 2%
Hepatocellular Carcinoma
6/46 13%
36/2210 2%
Retinoblastoma
1/27 4%
0/30 0%
Small Cell Lung Carcinoma
0/9 0%
13/752 2%
Non-Cancerous
2/104 2%
13/830 2%
Mesothelioma
3/62 5%
0/165 0%
Other Sarcomas
2/69 3%
8/699 1%
Biliary Tract Carcinoma
1/54 2%
12/950 1%
Head and Neck Carcinoma
7/85 8%
14/1574 1%
Glioma
4/52 8%
23/2127 1%
Esophageal Squamous Cell Carcinoma
5/51 10%
27/2550 1%
Thyroid Gland Carcinoma
2/45 4%
16/1592 1%
Ovarian Carcinoma
5/109 5%
7/998 1%
Neuroendocrine Tumour
4/154 3%
3/577 1%
Breast Carcinoma
2/144 1%
30/3264 1%
Adrenocortical Carcinoma
0/3 0%
1/112 1%
Kidney Carcinoma
3/85 4%
14/1862 1%

Mutation Distribution

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

Mutation counts by tissue
Mutation Distribution

How many mutations in PATJ 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 2,723 mutations in PATJ

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