ZNF83

Zinc finger protein 83 P51522 ZNF83_HUMAN
Protein Coding Chr 19 19q13.41 Swiss-Prot reviewed Entrez 55769
Mutations
1,029
CL 115 · Tissue 903
Samples
303
CL 40 · Tissue 258
Peptides
218
unique mutant peptides
Transcripts
10
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
Mutations1,029115903
Samples30340258
Peptides21843179

Function

ZNF83 · Zinc finger protein 83

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 be located in nucleus. [provided by Alliance of Genome Resources, Apr 2022]

Isoforms & Proteins

10 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
ENST00000301096 P51522 334 188
ENST00000597597 P51522 317 180
ENST00000545872 P51522 316 179
ENST00000597161 M0R3A5* 13 12
ENST00000596930 - 12 12
ENST00000594682 M0R287* 10 10
ENST00000600714 M0R287* 10 10
ENST00000601257 M0R287* 10 10
ENST00000536937 L0R8M2* 6 4
ENST00000598536 A0A994J561* 1 1

Gene Properties

Type
Protein Coding
Chromosome
19
Cytoband
19q13.41
Entrez ID
Aliases
HPF1ZNF816B

Recurrent Mutations

All 190 amino-acid changes on canonical ENST00000301096 · 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 ZNF83 · 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 ZNF83 – 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
Gastrointestinal Stromal Tumour
0/0 0%
6/133 5%
Chronic Myelogenous Leukemia
1/25 4%
0/0 0%
T-Cell Non-Hodgkins Lymphoma
1/26 4%
0/0 0%
Endometrial Carcinoma
3/42 7%
20/612 3%
Bladder Carcinoma
0/58 0%
35/956 4%
T-Lymphoblastic Leukemia
1/40 2%
0/0 0%
Rhabdomyosarcoma
0/33 0%
4/171 2%
Colorectal Carcinoma
5/143 4%
47/3239 1%
Hodgkins Lymphoma
1/16 6%
1/122 1%
Chondrosarcoma
0/14 0%
1/75 1%
Cervical Carcinoma
0/35 0%
5/422 1%
Esophageal Carcinoma
0/23 0%
8/769 1%
Squamous Cell Lung Carcinoma
2/57 4%
6/810 1%
Gastric Carcinoma
0/74 0%
16/1809 1%
Melanoma
2/210 1%
16/1899 1%
Non-Small Cell Lung Carcinoma
6/304 2%
8/1390 1%
Non-Cancerous
0/104 0%
7/830 1%
Other Sarcomas
1/69 1%
4/699 1%
Ewings Sarcoma
2/63 3%
0/262 0%
Neuroendocrine Tumour
1/154 1%
3/577 1%
Small Cell Lung Carcinoma
0/9 0%
4/752 1%
Germ Cell Tumour
1/25 4%
0/169 0%
Biliary Tract Carcinoma
2/54 4%
3/950 0%
Meningioma
1/3 33%
0/252 0%
Other Blood Cancers
1/61 2%
10/2725 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
10/2550 0%
Thyroid Gland Carcinoma
0/45 0%
6/1592 0%
Hepatocellular Carcinoma
2/46 4%
6/2210 0%
Breast Carcinoma
2/144 1%
10/3264 0%
Head and Neck Carcinoma
1/85 1%
4/1574 0%

Mutation Distribution

Where ZNF83 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in ZNF83 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 1,029 mutations in ZNF83

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