DET1

DET1 partner of COP1 E3 ubiquitin ligase Q7L5Y6 DET1_HUMAN
Protein Coding Chr 15 15q26.1 Swiss-Prot reviewed Entrez 55070
Mutations
981
CL 138 · Tissue 826
Samples
317
CL 62 · Tissue 248
Peptides
250
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
Mutations981138826
Samples31762248
Peptides25044208

Function

DET1 · DET1 partner of COP1 E3 ubiquitin ligase

Enables ubiquitin ligase-substrate adaptor activity and ubiquitin protein ligase binding activity. Involved in positive regulation of proteasomal ubiquitin-dependent protein catabolic process; protein ubiquitination; and protein-containing complex assembly. Part of Cul4A-RING E3 ubiquitin ligase complex. [provided by Alliance of Genome Resources, Apr 2022]

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
ENST00000268148 Q7L5Y6 336 230
ENST00000444300 Q7L5Y6-2 300 213
ENST00000564406 Q7L5Y6-2 300 213
ENST00000558413 H0YN79* 45 30

Gene Properties

Type
Protein Coding
Chromosome
15
Cytoband
15q26.1
Entrez ID

Recurrent Mutations

All 230 amino-acid changes on canonical ENST00000268148 · 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 DET1 · 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 DET1 – 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
4/40 10%
0/0 0%
Chronic Myelogenous Leukemia
2/25 8%
0/0 0%
Endometrial Carcinoma
4/42 10%
23/612 4%
Melanoma
3/210 1%
45/1899 2%
Oral Cavity Carcinoma
1/54 2%
0/0 0%
Squamous Cell Lung Carcinoma
3/57 5%
9/810 1%
Gastric Carcinoma
3/74 4%
23/1809 1%
Colorectal Carcinoma
7/143 5%
28/3239 1%
Other Solid Cancers
0/94 0%
15/1515 1%
Bladder Carcinoma
5/58 9%
4/956 0%
Non-Small Cell Lung Carcinoma
8/304 3%
7/1390 0%
Cervical Carcinoma
0/35 0%
4/422 1%
Mesothelioma
2/62 3%
0/165 0%
Biliary Tract Carcinoma
2/54 4%
6/950 1%
Hodgkins Lymphoma
0/16 0%
1/122 1%
Neuroendocrine Tumour
2/154 1%
3/577 1%
Other Sarcomas
4/69 6%
1/699 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
15/2550 1%
Ovarian Carcinoma
3/109 3%
3/998 0%
Head and Neck Carcinoma
1/85 1%
8/1574 1%
Germ Cell Tumour
0/25 0%
1/169 1%
Prostate Carcinoma
1/13 8%
10/2105 0%
Non-Cancerous
0/104 0%
4/830 0%
Pancreatic Carcinoma
1/89 1%
6/1611 0%
Small Cell Lung Carcinoma
0/9 0%
3/752 0%
Breast Carcinoma
1/144 1%
12/3264 0%
Glioma
0/52 0%
7/2127 0%
Plasma Cell Myeloma
1/44 2%
0/305 0%
Hepatocellular Carcinoma
0/46 0%
6/2210 0%
Medulloblastoma
0/0 0%
1/450 0%

Mutation Distribution

Where DET1 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in DET1 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 981 mutations in DET1

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