ZNF706

Zinc finger protein 706 Q9Y5V0 ZN706_HUMAN
Protein Coding Chr 8 8q22.3 Swiss-Prot reviewed Entrez 51123
Mutations
328
CL 18 · Tissue 310
Samples
45
CL 5 · Tissue 40
Peptides
23
unique mutant peptides
Transcripts
8
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
Mutations32818310
Samples45540
Peptides23420

Function

ZNF706 · Zinc finger protein 706

Predicted to enable metal ion binding activity. Predicted to be involved in negative regulation of stem cell population maintenance and negative regulation of transcription, DNA-templated. Predicted to be located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Apr 2022]

Isoforms & Proteins

8 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
ENST00000311212 Q9Y5V0 45 19
ENST00000517844 Q9Y5V0 42 19
ENST00000518336 Q9Y5V0 42 19
ENST00000519882 Q9Y5V0 42 19
ENST00000520347 Q9Y5V0 42 19
ENST00000520984 Q9Y5V0 42 19
ENST00000521272 Q9Y5V0 42 19
ENST00000519744 E5RHV4* 31 12

Gene Properties

Type
Protein Coding
Chromosome
8
Cytoband
8q22.3
Entrez ID
Aliases
HSPC038PNAS-106PNAS-113

Recurrent Mutations

All 19 amino-acid changes on canonical ENST00000311212 · 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 ZNF706 · 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 ZNF706 – 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
Osteosarcoma
0/45 0%
2/166 1%
Thyroid Gland Carcinoma
0/45 0%
7/1592 0%
Plasma Cell Myeloma
0/44 0%
1/305 0%
Hepatocellular Carcinoma
2/46 4%
4/2210 0%
Medulloblastoma
0/0 0%
1/450 0%
Other Solid Cancers
0/94 0%
3/1515 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
5/2550 0%
Non-Small Cell Lung Carcinoma
0/304 0%
3/1390 0%
Endometrial Carcinoma
0/42 0%
1/612 0%
Other Sarcomas
1/69 1%
0/699 0%
Squamous Cell Lung Carcinoma
0/57 0%
1/810 0%
Kidney Carcinoma
0/85 0%
2/1862 0%
Bladder Carcinoma
0/58 0%
1/956 0%
Melanoma
0/210 0%
2/1899 0%
Glioma
0/52 0%
2/2127 0%
Ovarian Carcinoma
0/109 0%
1/998 0%
B-Cell Non-Hodgkins Lymphoma
1/88 1%
1/2534 0%
Neuroblastoma
0/87 0%
1/1331 0%
Head and Neck Carcinoma
0/85 0%
1/1574 0%
Colorectal Carcinoma
1/143 1%
0/3239 0%
Breast Carcinoma
0/144 0%
1/3264 0%

Mutation Distribution

Where ZNF706 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in ZNF706 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 328 mutations in ZNF706

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