ZBTB3

Zinc finger and BTB domain containing 3 Q9H5J0 ZBTB3_HUMAN
Protein Coding Chr 11 11q12.3 Swiss-Prot reviewed Entrez 79842
Mutations
245
CL 63 · Tissue 174
Samples
224
CL 59 · Tissue 162
Peptides
183
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
Mutations24563174
Samples22459162
Peptides18338142

Function

ZBTB3 · Zinc finger and BTB domain containing 3

Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Apr 2022]

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
ENST00000673933 Q9H5J0 202 165
ENST00000394807 A0A6E1W9L1* 43 39

Gene Properties

Type
Protein Coding
Chromosome
11
Cytoband
11q12.3
Entrez ID

Recurrent Mutations

All 165 amino-acid changes on canonical ENST00000673933 · 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 ZBTB3 · 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 ZBTB3 – 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
4/40 10%
0/0 0%
Chronic Myelogenous Leukemia
1/25 4%
0/0 0%
T-Cell Non-Hodgkins Lymphoma
1/26 4%
0/0 0%
Endometrial Carcinoma
3/42 7%
7/612 1%
Gastrointestinal Stromal Tumour
0/0 0%
2/133 2%
Cervical Carcinoma
2/35 6%
4/422 1%
Non-Small Cell Lung Carcinoma
11/304 4%
11/1390 1%
Gastric Carcinoma
0/74 0%
18/1809 1%
Melanoma
3/210 1%
15/1899 1%
Squamous Cell Lung Carcinoma
1/57 2%
6/810 1%
Other Solid Cancers
0/94 0%
12/1515 1%
Breast Carcinoma
7/144 5%
17/3264 1%
Bladder Carcinoma
1/58 2%
6/956 1%
Non-Cancerous
0/104 0%
6/830 1%
Ewings Sarcoma
2/63 3%
0/262 0%
Head and Neck Carcinoma
1/85 1%
9/1574 1%
Colorectal Carcinoma
10/143 7%
10/3239 0%
Plasma Cell Myeloma
1/44 2%
1/305 0%
Osteosarcoma
1/45 2%
0/166 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
12/2550 0%
Other Sarcomas
0/69 0%
3/699 0%
Meningioma
0/3 0%
1/252 0%
Biliary Tract Carcinoma
1/54 2%
2/950 0%
Glioma
0/52 0%
6/2127 0%
Hepatocellular Carcinoma
0/46 0%
5/2210 0%
Wilms Tumour
0/5 0%
1/474 0%
Prostate Carcinoma
2/13 15%
2/2105 0%
Thyroid Gland Carcinoma
2/45 4%
1/1592 0%
B-Lymphoblastic Leukemia
2/55 4%
1/2640 0%
B-Cell Non-Hodgkins Lymphoma
2/88 2%
1/2534 0%

Mutation Distribution

Where ZBTB3 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in ZBTB3 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 245 mutations in ZBTB3

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