ZSCAN10

Zinc finger and SCAN domain containing 10 Q96SZ4 ZSC10_HUMAN
Protein Coding Chr 16 16p13.3 Swiss-Prot reviewed Entrez 84891
Mutations
1,816
CL 226 · Tissue 1,568
Samples
552
CL 119 · Tissue 426
Peptides
452
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
Mutations1,8162261,568
Samples552119426
Peptides452101380

Function

ZSCAN10 · Zinc finger and SCAN domain containing 10

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 negative regulation of transcription, DNA-templated and regulation of transcription by RNA polymerase II. Predicted to be located in nucleoplasm. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Apr 2022]

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
ENST00000576985 Q96SZ4 582 393
ENST00000252463 A0ABB0GZV6* 486 347
ENST00000538082 Q96SZ4-3 440 317
ENST00000575108 Q96SZ4-2 271 194
ENST00000572548 I3NI43* 37 31

Gene Properties

Type
Protein Coding
Chromosome
16
Cytoband
16p13.3
Entrez ID
Aliases
OFNSZFP206ZNF206

Recurrent Mutations

All 393 amino-acid changes on canonical ENST00000576985 · 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 ZSCAN10 · 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 ZSCAN10 – 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
9/40 22%
0/0 0%
Chronic Myelogenous Leukemia
2/25 8%
0/0 0%
Endometrial Carcinoma
4/42 10%
27/612 4%
Glioblastoma
4/98 4%
0/0 0%
Acute Monocytic Leukemia
1/1 100%
0/25 0%
Oral Cavity Carcinoma
2/54 4%
0/0 0%
Melanoma
5/210 2%
60/1899 3%
Gastrointestinal Stromal Tumour
0/0 0%
4/133 3%
Colorectal Carcinoma
20/143 14%
71/3239 2%
Other Solid Cancers
7/94 7%
30/1515 2%
Acute Myeloid Leukemia
2/90 2%
0/0 0%
Neuroendocrine Tumour
7/154 5%
7/577 1%
Adrenocortical Carcinoma
2/3 67%
0/112 0%
Gastric Carcinoma
4/74 5%
28/1809 2%
Non-Small Cell Lung Carcinoma
6/304 2%
22/1390 2%
Small Cell Lung Carcinoma
0/9 0%
12/752 2%
Pheochromocytoma and Paraganglioma
0/0 0%
1/71 1%
Thyroid Gland Carcinoma
1/45 2%
22/1592 1%
Squamous Cell Lung Carcinoma
0/57 0%
11/810 1%
Other Sarcomas
5/69 7%
4/699 1%
Chondrosarcoma
0/14 0%
1/75 1%
Bladder Carcinoma
2/58 3%
8/956 1%
Rhabdomyosarcoma
1/33 3%
1/171 1%
Biliary Tract Carcinoma
1/54 2%
8/950 1%
Burkitts Lymphoma
2/32 6%
0/196 0%
Plasma Cell Myeloma
1/44 2%
2/305 1%
Hepatocellular Carcinoma
5/46 11%
13/2210 1%
Ovarian Carcinoma
3/109 3%
5/998 0%
Hodgkins Lymphoma
1/16 6%
0/122 0%
Esophageal Squamous Cell Carcinoma
2/51 4%
16/2550 1%

Mutation Distribution

Where ZSCAN10 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in ZSCAN10 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 53 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 1,816 mutations in ZSCAN10

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