ZNF746

Zinc finger protein 746 Q6NUN9 ZN746_HUMAN
Protein Coding Chr 7 7q36.1 Swiss-Prot reviewed Entrez 155061
Mutations
1,159
CL 190 · Tissue 950
Samples
399
CL 112 · Tissue 280
Peptides
300
unique mutant peptides
Transcripts
5
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
Mutations1,159190950
Samples399112280
Peptides30064241

Function

ZNF746 · Zinc finger protein 746

Enables DNA-binding transcription repressor activity, RNA polymerase II-specific; RNA polymerase II cis-regulatory region sequence-specific DNA binding activity; and ubiquitin protein ligase binding activity. Involved in negative regulation of transcription by RNA polymerase II; positive regulation of neuron death; and positive regulation of transcription by RNA polymerase II. Located in cytosol and nucleoplasm. [provided by Alliance of Genome Resources, Apr 2022]

Isoforms & Proteins

5 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
ENST00000644635 A0A2R8YDQ5* 333 241
ENST00000340622 Q6NUN9 328 236
ENST00000685153 Q6NUN9-2 267 191
ENST00000458143 A0A8J9FQ52* 142 88
ENST00000461958 C9JNZ9* 89 62

Gene Properties

Type
Protein Coding
Chromosome
7
Cytoband
7q36.1
Entrez ID
Aliases
PARIS

Recurrent Mutations

All 236 amino-acid changes on canonical ENST00000340622 · 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 ZNF746 · 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 ZNF746 – 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
3/25 12%
0/0 0%
T-Cell Non-Hodgkins Lymphoma
2/26 8%
0/0 0%
Acute Myeloid Leukemia
5/90 6%
0/0 0%
Endometrial Carcinoma
8/42 19%
17/612 3%
Oral Cavity Carcinoma
2/54 4%
0/0 0%
Retinoblastoma
1/27 4%
0/30 0%
Colorectal Carcinoma
12/143 8%
47/3239 1%
Gastric Carcinoma
3/74 4%
29/1809 2%
Melanoma
8/210 4%
26/1899 1%
Thyroid Gland Carcinoma
2/45 4%
20/1592 1%
Other Solid Cancers
0/94 0%
21/1515 1%
Non-Small Cell Lung Carcinoma
8/304 3%
14/1390 1%
Bladder Carcinoma
0/58 0%
12/956 1%
Plasma Cell Myeloma
1/44 2%
3/305 1%
Squamous Cell Lung Carcinoma
2/57 4%
8/810 1%
Cervical Carcinoma
2/35 6%
3/422 1%
Neuroendocrine Tumour
6/154 4%
2/577 0%
Ovarian Carcinoma
2/109 2%
10/998 1%
Rhabdomyosarcoma
2/33 6%
0/171 0%
Gastrointestinal Stromal Tumour
0/0 0%
1/133 1%
Non-Cancerous
3/104 3%
3/830 0%
Neuroblastoma
8/87 9%
1/1331 0%
Head and Neck Carcinoma
3/85 4%
6/1574 0%
Other Sarcomas
1/69 1%
3/699 0%
Germ Cell Tumour
1/25 4%
0/169 0%
Esophageal Carcinoma
0/23 0%
4/769 1%
Pancreatic Carcinoma
2/89 2%
6/1611 0%
Kidney Carcinoma
2/85 2%
7/1862 0%
Burkitts Lymphoma
1/32 3%
0/196 0%

Mutation Distribution

Where ZNF746 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in ZNF746 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 1,159 mutations in ZNF746

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