ZNF254

Zinc finger protein 254 O75437 ZN254_HUMAN
Protein Coding Chr 19 19p12 Swiss-Prot reviewed Entrez 9534
Mutations
1,844
CL 214 · Tissue 1,608
Samples
451
CL 85 · Tissue 361
Peptides
347
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
Mutations1,8442141,608
Samples45185361
Peptides34760294

Function

ZNF254 · Zinc finger protein 254

Zinc finger proteins have been shown to interact with nucleic acids and to have diverse functions. The zinc finger domain is a conserved amino acid sequence motif containing 2 specifically positioned cysteines and 2 histidines that are involved in coordinating zinc. Kruppel-related proteins form 1 family of zinc finger proteins. See ZFP93 (MIM 604749) for additional information on zinc finger proteins.[supplied by OMIM, Jul 2002].

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
ENST00000357002 O75437 516 323
ENST00000613065 A0A087WZJ7* 437 286
ENST00000611359 A0A087X0A2* 420 272
ENST00000616028 F5H2M4* 408 264
ENST00000339642 F8W9V0* 63 44

Gene Properties

Type
Protein Coding
Chromosome
19
Cytoband
19p12
Entrez ID
Aliases
BMZF-5HD-ZNF1ZNF539ZNF91L

Recurrent Mutations

All 326 amino-acid changes on canonical ENST00000357002 · 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 ZNF254 · 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 ZNF254 – 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
Chronic Myelogenous Leukemia
3/25 12%
0/0 0%
Chordoma
1/7 14%
0/13 0%
Endometrial Carcinoma
2/42 5%
24/612 4%
Acute Myeloid Leukemia
3/90 3%
0/0 0%
Squamous Cell Lung Carcinoma
1/57 2%
20/810 2%
Melanoma
3/210 1%
46/1899 2%
Head and Neck Carcinoma
3/85 4%
27/1574 2%
Plasma Cell Myeloma
3/44 7%
3/305 1%
Small Cell Lung Carcinoma
2/9 22%
11/752 1%
Bladder Carcinoma
0/58 0%
17/956 2%
Meningioma
0/3 0%
4/252 2%
Cervical Carcinoma
0/35 0%
7/422 2%
Non-Small Cell Lung Carcinoma
9/304 3%
17/1390 1%
Colorectal Carcinoma
6/143 4%
45/3239 1%
Hodgkins Lymphoma
2/16 12%
0/122 0%
Esophageal Carcinoma
2/23 9%
9/769 1%
Gastric Carcinoma
4/74 5%
16/1809 1%
Germ Cell Tumour
0/25 0%
2/169 1%
Biliary Tract Carcinoma
1/54 2%
9/950 1%
Other Solid Cancers
3/94 3%
13/1515 1%
Neuroendocrine Tumour
2/154 1%
5/577 1%
Burkitts Lymphoma
1/32 3%
1/196 1%
Mesothelioma
0/62 0%
2/165 1%
Hepatocellular Carcinoma
0/46 0%
18/2210 1%
Other Sarcomas
3/69 4%
3/699 0%
Non-Cancerous
0/104 0%
7/830 1%
Gastrointestinal Stromal Tumour
0/0 0%
1/133 1%
Esophageal Squamous Cell Carcinoma
2/51 4%
17/2550 1%
Ovarian Carcinoma
6/109 6%
1/998 0%
Ewings Sarcoma
1/63 2%
1/262 0%

Mutation Distribution

Where ZNF254 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in ZNF254 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 1,844 mutations in ZNF254

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