ZBTB9

Zinc finger and BTB domain containing 9 Q96C00 ZBTB9_HUMAN
Protein Coding Chr 6 6p21.32 Swiss-Prot reviewed Entrez 221504
Mutations
190
CL 49 · Tissue 137
Samples
186
CL 49 · Tissue 133
Peptides
138
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
Mutations19049137
Samples18649133
Peptides13834111

Function

ZBTB9 · Zinc finger and BTB domain containing 9

Enables identical protein 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
ENST00000395064 Q96C00 189 137
ENST00000414934 Q96C00 1 1

Gene Properties

Type
Protein Coding
Chromosome
6
Cytoband
6p21.32
Entrez ID
Aliases
ZNF919

Recurrent Mutations

All 137 amino-acid changes on canonical ENST00000395064 · 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 ZBTB9 · 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 ZBTB9 – 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
5/40 12%
0/0 0%
Endometrial Carcinoma
4/42 10%
9/612 1%
Melanoma
4/210 2%
23/1899 1%
Germ Cell Tumour
2/25 8%
0/169 0%
Glioblastoma
1/98 1%
0/0 0%
Colorectal Carcinoma
11/143 8%
22/3239 1%
Non-Small Cell Lung Carcinoma
6/304 2%
6/1390 0%
Squamous Cell Lung Carcinoma
0/57 0%
6/810 1%
Head and Neck Carcinoma
2/85 2%
8/1574 1%
Other Solid Cancers
0/94 0%
9/1515 1%
Gastric Carcinoma
1/74 1%
9/1809 0%
Meningioma
0/3 0%
1/252 0%
Hepatocellular Carcinoma
0/46 0%
8/2210 0%
Biliary Tract Carcinoma
2/54 4%
1/950 0%
Bladder Carcinoma
0/58 0%
3/956 0%
Prostate Carcinoma
0/13 0%
6/2105 0%
Ovarian Carcinoma
1/109 1%
2/998 0%
Neuroendocrine Tumour
1/154 1%
1/577 0%
Pancreatic Carcinoma
1/89 1%
3/1611 0%
Glioma
0/52 0%
5/2127 0%
Medulloblastoma
0/0 0%
1/450 0%
Cervical Carcinoma
0/35 0%
1/422 0%
Esophageal Squamous Cell Carcinoma
2/51 4%
3/2550 0%
Breast Carcinoma
1/144 1%
4/3264 0%
B-Lymphoblastic Leukemia
3/55 5%
1/2640 0%
Other Sarcomas
0/69 0%
1/699 0%
Esophageal Carcinoma
0/23 0%
1/769 0%
Kidney Carcinoma
1/85 1%
1/1862 0%
B-Cell Non-Hodgkins Lymphoma
1/88 1%
1/2534 0%
Thyroid Gland Carcinoma
0/45 0%
1/1592 0%

Mutation Distribution

Where ZBTB9 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in ZBTB9 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.

Mutations

All 190 mutations in ZBTB9

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