ZBTB4

Zinc finger and BTB domain containing 4 Q9P1Z0 ZBTB4_HUMAN
Protein Coding Chr 17 17p13.1 Swiss-Prot reviewed Entrez 57659
Mutations
998
CL 136 · Tissue 834
Samples
489
CL 85 · Tissue 395
Peptides
382
unique mutant peptides
Transcripts
3
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
Mutations998136834
Samples48985395
Peptides38264319

Function

ZBTB4 · Zinc finger and BTB domain containing 4

Enables several functions, including DNA-binding transcription repressor activity, RNA polymerase II-specific; methyl-CpNpG binding activity; and sequence-specific DNA binding activity. Involved in cellular response to DNA damage stimulus and negative regulation of transcription by RNA polymerase II. Located in cytosol and nuclear body. [provided by Alliance of Genome Resources, Apr 2022]

Isoforms & Proteins

3 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
ENST00000380599 Q9P1Z0 529 382
ENST00000311403 Q9P1Z0 468 357
ENST00000639962 Q9P1Z0 1 1

Gene Properties

Type
Protein Coding
Chromosome
17
Cytoband
17p13.1
Entrez ID
Aliases
KAISO-L1ZNF903

Recurrent Mutations

All 382 amino-acid changes on canonical ENST00000380599 · 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 ZBTB4 · 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 ZBTB4 – 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%
Chronic Myelogenous Leukemia
2/25 8%
0/0 0%
Endometrial Carcinoma
4/42 10%
30/612 5%
T-Cell Non-Hodgkins Lymphoma
1/26 4%
0/0 0%
Gastrointestinal Stromal Tumour
0/0 0%
5/133 4%
Melanoma
2/210 1%
77/1899 4%
Oral Cavity Carcinoma
2/54 4%
0/0 0%
Colorectal Carcinoma
15/143 10%
62/3239 2%
Cervical Carcinoma
3/35 9%
7/422 2%
Hodgkins Lymphoma
2/16 12%
1/122 1%
Germ Cell Tumour
2/25 8%
2/169 1%
Gastric Carcinoma
4/74 5%
31/1809 2%
Other Solid Cancers
0/94 0%
30/1515 2%
Bladder Carcinoma
0/58 0%
17/956 2%
Squamous Cell Lung Carcinoma
0/57 0%
10/810 1%
Non-Small Cell Lung Carcinoma
6/304 2%
13/1390 1%
Acute Myeloid Leukemia
1/90 1%
0/0 0%
Ovarian Carcinoma
3/109 3%
8/998 1%
Adrenocortical Carcinoma
1/3 33%
0/112 0%
Plasma Cell Myeloma
2/44 5%
1/305 0%
Head and Neck Carcinoma
2/85 2%
12/1574 1%
Hepatocellular Carcinoma
3/46 7%
12/2210 1%
Esophageal Carcinoma
0/23 0%
5/769 1%
Glioma
0/52 0%
12/2127 1%
Neuroendocrine Tumour
3/154 2%
1/577 0%
Non-Cancerous
1/104 1%
4/830 0%
Other Sarcomas
2/69 3%
2/699 0%
Breast Carcinoma
3/144 2%
14/3264 0%
Biliary Tract Carcinoma
1/54 2%
4/950 0%
Thyroid Gland Carcinoma
2/45 4%
6/1592 0%

Mutation Distribution

Where ZBTB4 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in ZBTB4 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 998 mutations in ZBTB4

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