ZCCHC17

Zinc finger CCHC-type containing 17 Q9NP64 ZCC17_HUMAN
Protein Coding Chr 1 1p35.2 Swiss-Prot reviewed Entrez 51538
Mutations
635
CL 66 · Tissue 569
Samples
125
CL 18 · Tissue 107
Peptides
118
unique mutant peptides
Transcripts
8
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
Mutations63566569
Samples12518107
Peptides11819100

Function

ZCCHC17 · Zinc finger CCHC-type containing 17

Enables identical protein binding activity. Predicted to be involved in RNA stabilization. Predicted to be located in nucleolus. Predicted to be part of cytosolic large ribosomal subunit. [provided by Alliance of Genome Resources, Apr 2022]

Isoforms & Proteins

8 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
ENST00000344147 Q9NP64 109 75
ENST00000373714 Q9NP64 101 72
ENST00000615916 A0A087WXF8* 85 64
ENST00000627541 A0A0D9SEW3* 84 67
ENST00000546109 Q9NP64-3 81 64
ENST00000618216 A0A087WXU5* 66 46
ENST00000616393 A0A087WYV3* 60 48
ENST00000616859 A0A087WYF0* 49 41

Gene Properties

Type
Protein Coding
Chromosome
1
Cytoband
1p35.2
Entrez ID
Aliases
HSPC251PS1DpNO40

Recurrent Mutations

All 75 amino-acid changes on canonical ENST00000344147 · 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 ZCCHC17 · 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 ZCCHC17 – 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
2/25 8%
0/0 0%
T-Lymphoblastic Leukemia
3/40 8%
0/0 0%
Endometrial Carcinoma
3/42 7%
7/612 1%
Other Solid Cancers
0/94 0%
21/1515 1%
Melanoma
3/210 1%
18/1899 1%
Neuroendocrine Tumour
3/154 2%
2/577 0%
Germ Cell Tumour
0/25 0%
1/169 1%
Mesothelioma
1/62 2%
0/165 0%
Burkitts Lymphoma
0/32 0%
1/196 1%
Cervical Carcinoma
0/35 0%
2/422 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
10/2550 0%
Squamous Cell Lung Carcinoma
0/57 0%
3/810 0%
Colorectal Carcinoma
0/143 0%
11/3239 0%
Non-Cancerous
0/104 0%
3/830 0%
Bladder Carcinoma
0/58 0%
3/956 0%
Ovarian Carcinoma
1/109 1%
2/998 0%
Thyroid Gland Carcinoma
0/45 0%
4/1592 0%
Non-Small Cell Lung Carcinoma
1/304 0%
3/1390 0%
Kidney Carcinoma
0/85 0%
4/1862 0%
Gastric Carcinoma
0/74 0%
3/1809 0%
Hepatocellular Carcinoma
0/46 0%
3/2210 0%
Esophageal Carcinoma
0/23 0%
1/769 0%
Other Sarcomas
0/69 0%
1/699 0%
B-Cell Non-Hodgkins Lymphoma
0/88 0%
2/2534 0%
Head and Neck Carcinoma
0/85 0%
1/1574 0%
Glioma
0/52 0%
1/2127 0%
B-Lymphoblastic Leukemia
1/55 2%
0/2640 0%

Mutation Distribution

Where ZCCHC17 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in ZCCHC17 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 635 mutations in ZCCHC17

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