ZNF700

Zinc finger protein 700 Q9H0M5 ZN700_HUMAN
Protein Coding Chr 19 19p13.2 Swiss-Prot reviewed Entrez 90592
Mutations
1,302
CL 203 · Tissue 1,079
Samples
427
CL 91 · Tissue 327
Peptides
326
unique mutant peptides
Transcripts
3
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
Mutations1,3022031,079
Samples42791327
Peptides32663263

Function

ZNF700 · Zinc finger protein 700

Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription 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

3 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
ENST00000254321 Q9H0M5 466 310
ENST00000622593 A0A087WVH9* 421 299
ENST00000482090 K7EQV7* 415 293

Gene Properties

Type
Protein Coding
Chromosome
19
Cytoband
19p13.2
Entrez ID

Recurrent Mutations

All 310 amino-acid changes on canonical ENST00000254321 · 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 ZNF700 · 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 ZNF700 – 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
2/42 5%
25/612 4%
Glioblastoma
3/98 3%
0/0 0%
Thymic Epithelial Tumor
0/0 0%
1/39 3%
Unknown
1/10 10%
0/29 0%
Melanoma
8/210 4%
37/1899 2%
Cervical Carcinoma
6/35 17%
3/422 1%
Squamous Cell Lung Carcinoma
3/57 5%
14/810 2%
Bladder Carcinoma
3/58 5%
16/956 2%
Other Solid Cancers
0/94 0%
27/1515 2%
Colorectal Carcinoma
12/143 8%
43/3239 1%
Esophageal Carcinoma
0/23 0%
12/769 2%
Non-Small Cell Lung Carcinoma
11/304 4%
13/1390 1%
Gastric Carcinoma
5/74 7%
20/1809 1%
Chondrosarcoma
1/14 7%
0/75 0%
Neuroendocrine Tumour
6/154 4%
1/577 0%
Ewings Sarcoma
3/63 5%
0/262 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
22/2550 1%
Head and Neck Carcinoma
2/85 2%
12/1574 1%
Other Sarcomas
1/69 1%
5/699 1%
Hepatocellular Carcinoma
0/46 0%
17/2210 1%
Hodgkins Lymphoma
0/16 0%
1/122 1%
Kidney Carcinoma
1/85 1%
13/1862 1%
Plasma Cell Myeloma
0/44 0%
2/305 1%
Neuroblastoma
3/87 3%
5/1331 0%
Osteosarcoma
1/45 2%
0/166 0%
Breast Carcinoma
6/144 4%
10/3264 0%
B-Cell Non-Hodgkins Lymphoma
4/88 5%
8/2534 0%
Mesothelioma
1/62 2%
0/165 0%
Non-Cancerous
1/104 1%
3/830 0%
Pancreatic Carcinoma
2/89 2%
5/1611 0%

Mutation Distribution

Where ZNF700 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in ZNF700 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 1,302 mutations in ZNF700

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