WDR20

WD repeat domain 20 Q8TBZ3 WDR20_HUMAN
Protein Coding Chr 14 14q32.31 Swiss-Prot reviewed Entrez 91833
Mutations
1,282
CL 173 · Tissue 1,018
Samples
216
CL 42 · Tissue 167
Peptides
197
unique mutant peptides
Transcripts
9
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
Mutations1,2821731,018
Samples21642167
Peptides19733157

Function

WDR20 · WD repeat domain 20

This gene encodes a WD repeat-containing protein that functions to preserve and regulate the activity of the USP12-UAF1 deubiquitinating enzyme complex. Multiple alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jun 2011].

Isoforms & Proteins

9 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
ENST00000342702 Q8TBZ3 210 165
ENST00000424963 A0A088AWN2* 200 162
ENST00000335263 Q8TBZ3-2 199 161
ENST00000454394 Q8TBZ3-7 195 162
ENST00000556807 Q8TBZ3-6 179 141
ENST00000556511 Q8TBZ3-5 173 140
ENST00000322340 Q8TBZ3-3 56 50
ENST00000558567 H0YKE8* 45 38
ENST00000299135 Q8TBZ3-8 25 19

Gene Properties

Type
Protein Coding
Chromosome
14
Cytoband
14q32.31
Entrez ID
Aliases
Bun107DMR

Recurrent Mutations

All 165 amino-acid changes on canonical ENST00000342702 · 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 WDR20 · 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 WDR20 – 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
3/40 8%
0/0 0%
Endometrial Carcinoma
3/42 7%
9/612 1%
Hodgkins Lymphoma
0/16 0%
2/122 2%
Melanoma
4/210 2%
26/1899 1%
Acute Myeloid Leukemia
1/90 1%
0/0 0%
Colorectal Carcinoma
7/143 5%
27/3239 1%
Gastric Carcinoma
3/74 4%
15/1809 1%
Bladder Carcinoma
0/58 0%
9/956 1%
Burkitts Lymphoma
2/32 6%
0/196 0%
Gastrointestinal Stromal Tumour
0/0 0%
1/133 1%
Cervical Carcinoma
0/35 0%
3/422 1%
Non-Small Cell Lung Carcinoma
2/304 1%
9/1390 1%
Other Solid Cancers
0/94 0%
9/1515 1%
Germ Cell Tumour
0/25 0%
1/169 1%
Ovarian Carcinoma
1/109 1%
4/998 0%
Mesothelioma
1/62 2%
0/165 0%
Head and Neck Carcinoma
3/85 4%
4/1574 0%
Biliary Tract Carcinoma
1/54 2%
3/950 0%
Hepatocellular Carcinoma
0/46 0%
9/2210 0%
Squamous Cell Lung Carcinoma
0/57 0%
3/810 0%
Prostate Carcinoma
0/13 0%
7/2105 0%
Non-Cancerous
0/104 0%
3/830 0%
Kidney Carcinoma
0/85 0%
6/1862 0%
Breast Carcinoma
3/144 2%
7/3264 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
5/2550 0%
Glioma
1/52 2%
3/2127 0%
Neuroendocrine Tumour
1/154 1%
0/577 0%
Small Cell Lung Carcinoma
0/9 0%
1/752 0%
Esophageal Carcinoma
0/23 0%
1/769 0%
Other Sarcomas
0/69 0%
1/699 0%

Mutation Distribution

Where WDR20 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in WDR20 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 1,282 mutations in WDR20

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