PCDH11Y

Protocadherin 11 Y-linked Q9BZA8 PC11Y_HUMAN
Protein Coding Chr Y Yp11.2 Swiss-Prot reviewed Entrez 83259
Mutations
1,836
CL 220 · Tissue 1,600
Samples
389
CL 44 · Tissue 341
Peptides
348
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
Mutations1,8362201,600
Samples38944341
Peptides34841314

Function

PCDH11Y · Protocadherin 11 Y-linked

This gene belongs to the protocadherin family, a subfamily of the cadherin superfamily. The encoded protein consists of an extracellular domain containing seven cadherin repeats, a transmembrane domain, and a cytoplasmic tail that differs from those of the classical cadherins. This gene is located on the Y chromosome in a block of X/Y homology and is very closely related to its paralog on the X chromosome. The protein is thought to play a role in cell-cell recognition during development of the central nervous system. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2013].

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
ENST00000400457 Q9BZA8 447 336
ENST00000215473 Q9BZA8-4 353 258
ENST00000362095 Q9BZA8-2 352 257
ENST00000333703 Q9BZA8-3 342 247
ENST00000622698 Q9BZA8-3 342 247

Gene Properties

Type
Protein Coding
Chromosome
Y
Cytoband
Yp11.2
Entrez ID
Aliases
PCDH-PCPCDH22PCDHXPCDHY

Recurrent Mutations

All 336 amino-acid changes on canonical ENST00000400457 · 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 PCDH11Y · 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 PCDH11Y – 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
Chronic Myelogenous Leukemia
1/25 4%
0/0 0%
Squamous Cell Lung Carcinoma
2/57 4%
29/810 4%
Non-Small Cell Lung Carcinoma
17/304 6%
29/1390 2%
Melanoma
2/210 1%
54/1899 3%
T-Lymphoblastic Leukemia
1/40 2%
0/0 0%
Esophageal Carcinoma
0/23 0%
15/769 2%
Oral Cavity Carcinoma
1/54 2%
0/0 0%
Small Cell Lung Carcinoma
0/9 0%
13/752 2%
Mesothelioma
2/62 3%
1/165 1%
Bladder Carcinoma
0/58 0%
13/956 1%
Gastric Carcinoma
1/74 1%
23/1809 1%
Colorectal Carcinoma
2/143 1%
37/3239 1%
Chondrosarcoma
0/14 0%
1/75 1%
Other Solid Cancers
1/94 1%
17/1515 1%
Hepatocellular Carcinoma
0/46 0%
25/2210 1%
Neuroendocrine Tumour
7/154 5%
1/577 0%
Glioma
0/52 0%
19/2127 1%
Gastrointestinal Stromal Tumour
0/0 0%
1/133 1%
Biliary Tract Carcinoma
0/54 0%
7/950 1%
Other Sarcomas
1/69 1%
4/699 1%
Thyroid Gland Carcinoma
0/45 0%
9/1592 1%
Rhabdomyosarcoma
0/33 0%
1/171 1%
Osteosarcoma
1/45 2%
0/166 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
12/2550 0%
Burkitts Lymphoma
1/32 3%
0/196 0%
Head and Neck Carcinoma
0/85 0%
7/1574 0%
Prostate Carcinoma
0/13 0%
9/2105 0%
Non-Cancerous
0/104 0%
3/830 0%
Neuroblastoma
1/87 1%
3/1331 0%
Kidney Carcinoma
1/85 1%
3/1862 0%

Mutation Distribution

Where PCDH11Y is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in PCDH11Y 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 42 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 1,836 mutations in PCDH11Y

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