ZP4

Zona pellucida glycoprotein 4 Q12836 ZP4_HUMAN
Protein Coding Chr 1 1q43 Swiss-Prot reviewed Entrez 57829
Mutations
1,273
CL 260 · Tissue 996
Samples
625
CL 161 · Tissue 455
Peptides
456
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
Mutations1,273260996
Samples625161455
Peptides45698375

Function

ZP4 · Zona pellucida glycoprotein 4

The zona pellucida is an extracellular matrix that surrounds the oocyte and early embryo. It is composed primarily of three or four glycoproteins with various functions during fertilization and preimplantation development. The nascent protein contains a N-terminal signal peptide sequence, a conserved ZP domain, a consensus furin cleavage site, and a C-terminal transmembrane domain. It is hypothesized that furin cleavage results in release of the mature protein from the plasma membrane for subsequent incorporation into the zona pellucida matrix. However, the requirement for furin cleavage in this process remains controversial based on mouse studies. Previously, this gene has been referred to as ZP1 or ZPB and thought to have similar functions as mouse Zp1. However, a human gene with higher similarity and chromosomal synteny to mouse Zp1 has been assigned the symbol ZP1 and this gene has been assigned the symbol ZP4. [provided by RefSeq, Jul 2008].

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
ENST00000366570 Q12836 672 452
ENST00000611898 Q12836 601 436

Gene Properties

Type
Protein Coding
Chromosome
1
Cytoband
1q43
Entrez ID
Aliases
ZBPZP1ZP1BZPBZPB2Zp-4

Recurrent Mutations

All 452 amino-acid changes on canonical ENST00000366570 · 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 ZP4 · 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 ZP4 – 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
Non-Small Cell Lung Carcinoma
52/304 17%
72/1390 5%
Acute Myeloid Leukemia
4/90 4%
0/0 0%
Glioblastoma
4/98 4%
0/0 0%
Oral Cavity Carcinoma
2/54 4%
0/0 0%
Squamous Cell Lung Carcinoma
3/57 5%
27/810 3%
Melanoma
13/210 6%
59/1899 3%
Endometrial Carcinoma
4/42 10%
18/612 3%
Neuroendocrine Tumour
14/154 9%
7/577 1%
Thymic Epithelial Tumor
0/0 0%
1/39 3%
Small Cell Lung Carcinoma
0/9 0%
19/752 3%
T-Lymphoblastic Leukemia
1/40 2%
0/0 0%
Gastric Carcinoma
5/74 7%
26/1809 1%
Colorectal Carcinoma
8/143 6%
47/3239 1%
Germ Cell Tumour
2/25 8%
1/169 1%
Gastrointestinal Stromal Tumour
0/0 0%
2/133 2%
Hodgkins Lymphoma
0/16 0%
2/122 2%
Plasma Cell Myeloma
3/44 7%
2/305 1%
Other Sarcomas
3/69 4%
7/699 1%
Non-Cancerous
1/104 1%
9/830 1%
Other Solid Cancers
0/94 0%
17/1515 1%
Esophageal Carcinoma
0/23 0%
8/769 1%
Biliary Tract Carcinoma
4/54 7%
6/950 1%
Ovarian Carcinoma
5/109 5%
5/998 0%
Hepatocellular Carcinoma
1/46 2%
19/2210 1%
Adrenocortical Carcinoma
0/3 0%
1/112 1%
B-Cell Non-Hodgkins Lymphoma
9/88 10%
13/2534 1%
Bladder Carcinoma
1/58 2%
7/956 1%
Breast Carcinoma
3/144 2%
21/3264 1%
Thyroid Gland Carcinoma
2/45 4%
9/1592 1%
Cervical Carcinoma
0/35 0%
3/422 1%

Mutation Distribution

Where ZP4 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in ZP4 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 1 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 1,273 mutations in ZP4

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