ANGPT4

Angiopoietin 4 Q9Y264 ANGP4_HUMAN
Protein Coding Chr 20 20p13 Swiss-Prot reviewed Entrez 51378
Mutations
357
CL 60 · Tissue 292
Samples
334
CL 54 · Tissue 276
Peptides
248
unique mutant peptides
Transcripts
1
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
Mutations35760292
Samples33454276
Peptides24841215

Function

ANGPT4 · Angiopoietin 4

Angiopoietins are proteins with important roles in vascular development and angiogenesis. All angiopoietins bind with similar affinity to an endothelial cell-specific tyrosine-protein kinase receptor. The mechanism by which they contribute to angiogenesis is thought to involve regulation of endothelial cell interactions with supporting perivascular cells. The protein encoded by this gene functions as an agonist and is an angiopoietin. [provided by RefSeq, Jul 2008].

Isoforms & Proteins

1 transcript · 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
ENST00000381922 Q9Y264 357 248

Gene Properties

Type
Protein Coding
Chromosome
20
Cytoband
20p13
Entrez ID
Aliases
ANG3ANG4

Recurrent Mutations

All 248 amino-acid changes on canonical ENST00000381922 · 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 ANGPT4 · 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 ANGPT4 – 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
6/40 15%
0/0 0%
Melanoma
4/210 2%
44/1899 2%
Glioblastoma
2/98 2%
0/0 0%
Squamous Cell Lung Carcinoma
6/57 11%
11/810 1%
Small Cell Lung Carcinoma
0/9 0%
14/752 2%
Non-Small Cell Lung Carcinoma
6/304 2%
24/1390 2%
Endometrial Carcinoma
1/42 2%
10/612 2%
Hodgkins Lymphoma
0/16 0%
2/122 2%
Meningioma
0/3 0%
3/252 1%
Colorectal Carcinoma
7/143 5%
33/3239 1%
Gastric Carcinoma
0/74 0%
20/1809 1%
Other Solid Cancers
2/94 2%
14/1515 1%
Other Sarcomas
2/69 3%
5/699 1%
Bladder Carcinoma
0/58 0%
9/956 1%
Thyroid Gland Carcinoma
2/45 4%
10/1592 1%
Head and Neck Carcinoma
2/85 2%
10/1574 1%
Neuroendocrine Tumour
2/154 1%
2/577 0%
Non-Cancerous
1/104 1%
4/830 0%
Glioma
2/52 4%
9/2127 0%
Medulloblastoma
0/0 0%
2/450 0%
Breast Carcinoma
0/144 0%
13/3264 0%
Hepatocellular Carcinoma
0/46 0%
8/2210 0%
Kidney Carcinoma
1/85 1%
5/1862 0%
Pancreatic Carcinoma
1/89 1%
4/1611 0%
Plasma Cell Myeloma
0/44 0%
1/305 0%
B-Cell Non-Hodgkins Lymphoma
1/88 1%
6/2534 0%
Ovarian Carcinoma
1/109 1%
2/998 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
6/2550 0%
Cervical Carcinoma
0/35 0%
1/422 0%
Neuroblastoma
1/87 1%
2/1331 0%

Mutation Distribution

Where ANGPT4 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in ANGPT4 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 357 mutations in ANGPT4

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