ZWINT

ZW10 interacting kinetochore protein O95229 ZWINT_HUMAN
Protein Coding Chr 10 10q21.1 Swiss-Prot reviewed Entrez 11130
Mutations
626
CL 58 · Tissue 564
Samples
193
CL 25 · Tissue 166
Peptides
173
unique mutant peptides
Transcripts
4
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
Mutations62658564
Samples19325166
Peptides17320157

Function

ZWINT · ZW10 interacting kinetochore protein

This gene encodes a protein that is clearly involved in kinetochore function although an exact role is not known. It interacts with ZW10, another kinetochore protein, possibly regulating the association between ZW10 and kinetochores. The encoded protein localizes to prophase kinetochores before ZW10 does and it remains detectable on the kinetochore until late anaphase. It has a uniform distribution in the cytoplasm of interphase cells. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008].

Isoforms & Proteins

4 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
ENST00000373944 O95229 196 148
ENST00000395405 O95229 182 142
ENST00000361148 O95229-2 132 114
ENST00000318387 A6NH27* 116 84

Gene Properties

Type
Protein Coding
Chromosome
10
Cytoband
10q21.1
Entrez ID
Aliases
HZwint-1KNTC2APSIP30ZWINT1

Recurrent Mutations

All 148 amino-acid changes on canonical ENST00000373944 · 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 ZWINT · 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 ZWINT – 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-Cell Non-Hodgkins Lymphoma
1/26 4%
0/0 0%
Gastrointestinal Stromal Tumour
0/0 0%
5/133 4%
Endometrial Carcinoma
4/42 10%
12/612 2%
Burkitts Lymphoma
0/32 0%
3/196 2%
Non-Small Cell Lung Carcinoma
5/304 2%
17/1390 1%
Squamous Cell Lung Carcinoma
0/57 0%
9/810 1%
Glioblastoma
1/98 1%
0/0 0%
Gastric Carcinoma
0/74 0%
19/1809 1%
Plasma Cell Myeloma
1/44 2%
2/305 1%
Colorectal Carcinoma
2/143 1%
23/3239 1%
Cervical Carcinoma
0/35 0%
3/422 1%
Melanoma
2/210 1%
11/1899 1%
Bladder Carcinoma
0/58 0%
5/956 1%
Wilms Tumour
0/5 0%
2/474 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
11/2550 0%
Small Cell Lung Carcinoma
0/9 0%
3/752 0%
Head and Neck Carcinoma
0/85 0%
6/1574 0%
Breast Carcinoma
4/144 3%
7/3264 0%
Neuroblastoma
1/87 1%
3/1331 0%
Esophageal Carcinoma
0/23 0%
2/769 0%
Glioma
0/52 0%
5/2127 0%
Hepatocellular Carcinoma
3/46 7%
2/2210 0%
Ovarian Carcinoma
1/109 1%
1/998 0%
Prostate Carcinoma
0/13 0%
3/2105 0%
Neuroendocrine Tumour
0/154 0%
1/577 0%
B-Cell Non-Hodgkins Lymphoma
0/88 0%
3/2534 0%
Other Blood Cancers
0/61 0%
3/2725 0%
Kidney Carcinoma
0/85 0%
2/1862 0%
Biliary Tract Carcinoma
0/54 0%
1/950 0%
B-Lymphoblastic Leukemia
0/55 0%
2/2640 0%

Mutation Distribution

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

Mutation counts by tissue
Mutation Distribution

How many mutations in ZWINT 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 626 mutations in ZWINT

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