ZNF544

Zinc finger protein 544 Q6NX49 ZN544_HUMAN
Protein Coding Chr 19 19q13.43 Swiss-Prot reviewed Entrez 27300
Mutations
1,637
CL 244 · Tissue 1,388
Samples
322
CL 71 · Tissue 247
Peptides
293
unique mutant peptides
Transcripts
12
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
Mutations1,6372441,388
Samples32271247
Peptides29355236

Function

ZNF544 · Zinc finger protein 544

Predicted to enable DNA-binding transcription activator 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 be active in nucleus. [provided by Alliance of Genome Resources, Apr 2022]

Isoforms & Proteins

12 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
ENST00000596652 Q6NX49 307 253
ENST00000269829 Q6NX49 303 249
ENST00000600044 J3KQC8* 299 245
ENST00000600220 J3KQC8* 298 244
ENST00000599953 M0QY11* 251 202
ENST00000627781 A0A0D9SEJ3* 31 27
ENST00000687789 Q6NX49 31 30
ENST00000595981 M0QZY0* 27 23
ENST00000596929 M0QZM7* 24 21
ENST00000594384 M0R2F0* 22 19
ENST00000596825 M0R2F0* 22 19
ENST00000599227 M0R2F0* 22 19

Gene Properties

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

Recurrent Mutations

All 253 amino-acid changes on canonical ENST00000596652 · 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 ZNF544 · 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 ZNF544 – 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
3/40 8%
0/0 0%
Oral Cavity Carcinoma
3/54 6%
0/0 0%
Thymic Epithelial Tumor
0/0 0%
2/39 5%
Gastrointestinal Stromal Tumour
0/0 0%
5/133 4%
Endometrial Carcinoma
4/42 10%
19/612 3%
Hodgkins Lymphoma
3/16 19%
1/122 1%
Melanoma
1/210 0%
32/1899 2%
Colorectal Carcinoma
17/143 12%
35/3239 1%
Cervical Carcinoma
0/35 0%
7/422 2%
Osteosarcoma
3/45 7%
0/166 0%
Bladder Carcinoma
0/58 0%
14/956 1%
Burkitts Lymphoma
0/32 0%
3/196 2%
Other Solid Cancers
0/94 0%
17/1515 1%
Glioblastoma
1/98 1%
0/0 0%
Gastric Carcinoma
2/74 3%
16/1809 1%
Squamous Cell Lung Carcinoma
2/57 4%
6/810 1%
Non-Small Cell Lung Carcinoma
7/304 2%
6/1390 0%
Breast Carcinoma
2/144 1%
19/3264 1%
Ewings Sarcoma
2/63 3%
0/262 0%
Esophageal Squamous Cell Carcinoma
2/51 4%
13/2550 1%
Germ Cell Tumour
1/25 4%
0/169 0%
Neuroblastoma
2/87 2%
5/1331 0%
Head and Neck Carcinoma
0/85 0%
8/1574 1%
Medulloblastoma
0/0 0%
2/450 0%
Wilms Tumour
0/5 0%
2/474 0%
Glioma
0/52 0%
9/2127 0%
Neuroendocrine Tumour
3/154 2%
0/577 0%
Ovarian Carcinoma
2/109 2%
2/998 0%
Kidney Carcinoma
2/85 2%
5/1862 0%
Biliary Tract Carcinoma
0/54 0%
3/950 0%

Mutation Distribution

Where ZNF544 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in ZNF544 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 1,637 mutations in ZNF544

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