ZFP14

ZFP14 zinc finger protein Q9HCL3 ZFP14_HUMAN
Protein Coding Chr 19 19q13.12 Swiss-Prot reviewed Entrez 57677
Mutations
335
CL 63 · Tissue 268
Samples
271
CL 54 · Tissue 214
Peptides
224
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
Mutations33563268
Samples27154214
Peptides22440184

Function

ZFP14 · ZFP14 zinc finger protein

Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to act upstream of or within blastocyst hatching. 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
ENST00000270001 Q9HCL3 292 211
ENST00000589280 K7EM99* 43 35

Gene Properties

Type
Protein Coding
Chromosome
19
Cytoband
19q13.12
Entrez ID
Aliases
ZNF531

Recurrent Mutations

All 211 amino-acid changes on canonical ENST00000270001 · 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 ZFP14 · 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 ZFP14 – 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
Endometrial Carcinoma
6/42 14%
21/612 3%
Melanoma
3/210 1%
36/1899 2%
Plasma Cell Myeloma
3/44 7%
2/305 1%
Squamous Cell Lung Carcinoma
1/57 2%
11/810 1%
Colorectal Carcinoma
14/143 10%
30/3239 1%
Non-Small Cell Lung Carcinoma
6/304 2%
16/1390 1%
Neuroendocrine Tumour
6/154 4%
3/577 1%
Gastric Carcinoma
1/74 1%
19/1809 1%
Other Solid Cancers
0/94 0%
12/1515 1%
Ewings Sarcoma
1/63 2%
1/262 0%
Head and Neck Carcinoma
3/85 4%
7/1574 0%
Bladder Carcinoma
0/58 0%
6/956 1%
Biliary Tract Carcinoma
0/54 0%
5/950 1%
Cervical Carcinoma
0/35 0%
2/422 0%
Mesothelioma
1/62 2%
0/165 0%
Esophageal Carcinoma
0/23 0%
3/769 0%
Non-Cancerous
0/104 0%
3/830 0%
Pancreatic Carcinoma
2/89 2%
3/1611 0%
Hepatocellular Carcinoma
0/46 0%
6/2210 0%
Other Sarcomas
0/69 0%
2/699 0%
Kidney Carcinoma
0/85 0%
4/1862 0%
Breast Carcinoma
2/144 1%
5/3264 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
5/2550 0%
Ovarian Carcinoma
1/109 1%
1/998 0%
Thyroid Gland Carcinoma
0/45 0%
3/1592 0%
Neuroblastoma
0/87 0%
2/1331 0%
Glioma
0/52 0%
3/2127 0%
Small Cell Lung Carcinoma
0/9 0%
1/752 0%
B-Cell Non-Hodgkins Lymphoma
1/88 1%
2/2534 0%
B-Lymphoblastic Leukemia
3/55 5%
0/2640 0%

Mutation Distribution

Where ZFP14 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in ZFP14 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 335 mutations in ZFP14

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