ZBTB7B

Zinc finger and BTB domain containing 7B O15156 ZBT7B_HUMAN
Protein Coding Chr 1 1q21.3 Swiss-Prot reviewed Entrez 51043
Mutations
1,328
CL 142 · Tissue 1,060
Samples
331
CL 68 · Tissue 259
Peptides
275
unique mutant peptides
Transcripts
4
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
Mutations1,3281421,060
Samples33168259
Peptides27541209

Function

ZBTB7B · Zinc finger and BTB domain containing 7B

This gene encodes a zinc finger-containing transcription factor that acts as a key regulator of lineage commitment of immature T-cell precursors. It is necessary and sufficient for commitment of CD4 lineage, while its absence causes CD8 commitment. It also functions as a transcriptional repressor of type I collagen genes. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jan 2012].

Isoforms & Proteins

4 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
ENST00000535420 O15156 365 262
ENST00000417934 O15156-2 327 254
ENST00000292176 O15156 318 246
ENST00000368426 O15156 318 246

Gene Properties

Type
Protein Coding
Chromosome
1
Cytoband
1q21.3
Entrez ID
Aliases
CKROXTHPOKZBTB15ZFP-67ZFP67ZNF857B

Recurrent Mutations

All 262 amino-acid changes on canonical ENST00000535420 · 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 ZBTB7B · 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 ZBTB7B – 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
Chordoma
1/7 14%
0/13 0%
Endometrial Carcinoma
6/42 14%
24/612 4%
Glioblastoma
4/98 4%
0/0 0%
Chronic Myelogenous Leukemia
1/25 4%
0/0 0%
Oral Cavity Carcinoma
2/54 4%
0/0 0%
Other Solid Cancers
3/94 3%
21/1515 1%
Colorectal Carcinoma
11/143 8%
34/3239 1%
Melanoma
2/210 1%
26/1899 1%
Bladder Carcinoma
0/58 0%
13/956 1%
Squamous Cell Lung Carcinoma
3/57 5%
8/810 1%
Gastric Carcinoma
2/74 3%
22/1809 1%
Non-Cancerous
1/104 1%
10/830 1%
Acute Myeloid Leukemia
1/90 1%
0/0 0%
Germ Cell Tumour
0/25 0%
2/169 1%
Plasma Cell Myeloma
2/44 5%
1/305 0%
Esophageal Squamous Cell Carcinoma
2/51 4%
20/2550 1%
Non-Small Cell Lung Carcinoma
2/304 1%
12/1390 1%
Ovarian Carcinoma
5/109 5%
3/998 0%
Neuroendocrine Tumour
3/154 2%
2/577 0%
Head and Neck Carcinoma
3/85 4%
7/1574 0%
Kidney Carcinoma
1/85 1%
8/1862 0%
Cervical Carcinoma
0/35 0%
2/422 0%
Hepatocellular Carcinoma
1/46 2%
8/2210 0%
Other Sarcomas
0/69 0%
3/699 0%
Thyroid Gland Carcinoma
0/45 0%
6/1592 0%
Breast Carcinoma
2/144 1%
9/3264 0%
B-Cell Non-Hodgkins Lymphoma
1/88 1%
6/2534 0%
Small Cell Lung Carcinoma
0/9 0%
2/752 0%
Prostate Carcinoma
0/13 0%
5/2105 0%
Biliary Tract Carcinoma
0/54 0%
2/950 0%

Mutation Distribution

Where ZBTB7B is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in ZBTB7B 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 1,328 mutations in ZBTB7B

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