ZNF274

Zinc finger protein 274 Q96GC6 ZN274_HUMAN
Protein Coding Chr 19 19q13.43 Swiss-Prot reviewed Entrez 10782
Mutations
1,390
CL 203 · Tissue 1,172
Samples
307
CL 62 · Tissue 240
Peptides
243
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
Mutations1,3902031,172
Samples30762240
Peptides24344203

Function

ZNF274 · Zinc finger protein 274

This gene encodes a zinc finger protein containing five C2H2-type zinc finger domains, one or two Kruppel-associated box A (KRAB A) domains, and a leucine-rich domain. The encoded protein has been suggested to be a transcriptional repressor. It localizes predominantly to the nucleolus. Alternatively spliced transcript variants encoding different isoforms exist. These variants utilize alternative polyadenylation signals. [provided by RefSeq, Jul 2008].

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
ENST00000617501 Q96GC6 324 234
ENST00000610905 Q96GC6 286 216
ENST00000345813 Q96GC6-2 272 206
ENST00000326804 A0A0A0MR47* 268 201
ENST00000424679 Q96GC6-3 240 184

Gene Properties

Type
Protein Coding
Chromosome
19
Cytoband
19q13.43
Entrez ID
Aliases
HFB101ZF2ZKSCAN19ZSCAN51

Recurrent Mutations

All 234 amino-acid changes on canonical ENST00000617501 · 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 ZNF274 · 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 ZNF274 – 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%
Chronic Myelogenous Leukemia
2/25 8%
0/0 0%
Oral Cavity Carcinoma
2/54 4%
0/0 0%
Endometrial Carcinoma
3/42 7%
14/612 2%
Melanoma
2/210 1%
38/1899 2%
Squamous Cell Lung Carcinoma
2/57 4%
12/810 1%
Bladder Carcinoma
3/58 5%
13/956 1%
Colorectal Carcinoma
10/143 7%
35/3239 1%
Other Solid Cancers
3/94 3%
16/1515 1%
Gastric Carcinoma
2/74 3%
20/1809 1%
Acute Myeloid Leukemia
1/90 1%
0/0 0%
Neuroendocrine Tumour
8/154 5%
0/577 0%
Esophageal Squamous Cell Carcinoma
3/51 6%
18/2550 1%
Hodgkins Lymphoma
0/16 0%
1/122 1%
Non-Small Cell Lung Carcinoma
3/304 1%
9/1390 1%
Small Cell Lung Carcinoma
0/9 0%
5/752 1%
Cervical Carcinoma
2/35 6%
1/422 0%
Esophageal Carcinoma
1/23 4%
4/769 1%
Plasma Cell Myeloma
1/44 2%
1/305 0%
Mesothelioma
0/62 0%
1/165 1%
Head and Neck Carcinoma
0/85 0%
7/1574 0%
Glioma
1/52 2%
8/2127 0%
Biliary Tract Carcinoma
0/54 0%
4/950 0%
Breast Carcinoma
3/144 2%
10/3264 0%
Thyroid Gland Carcinoma
0/45 0%
6/1592 0%
Non-Cancerous
1/104 1%
2/830 0%
Ewings Sarcoma
0/63 0%
1/262 0%
Hepatocellular Carcinoma
1/46 2%
5/2210 0%
Kidney Carcinoma
0/85 0%
5/1862 0%
Pancreatic Carcinoma
0/89 0%
3/1611 0%

Mutation Distribution

Where ZNF274 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in ZNF274 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 1,390 mutations in ZNF274

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