DICER1

Dicer 1, ribonuclease III Q9UPY3 DICER_HUMAN
Protein Coding Chr 14 14q32.13 Swiss-Prot reviewed Entrez 23405
Mutations
4,304
CL 424 · Tissue 3,846
Samples
846
CL 132 · Tissue 703
Peptides
712
unique mutant peptides
Transcripts
7
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
Mutations4,3044243,846
Samples846132703
Peptides71297619

Function

DICER1 · Dicer 1, ribonuclease III

This gene encodes a protein possessing an RNA helicase motif containing a DEXH box in its amino terminus and an RNA motif in the carboxy terminus. The encoded protein functions as a ribonuclease and is required by the RNA interference and small temporal RNA (stRNA) pathways to produce the active small RNA component that represses gene expression. This protein also acts as a strong antiviral agent with activity against RNA viruses, including the Zika and SARS-CoV-2 viruses. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2021].

Isoforms & Proteins

7 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
ENST00000343455 Q9UPY3 950 676
ENST00000393063 Q9UPY3 853 635
ENST00000526495 Q9UPY3 853 635
ENST00000527414 Q9UPY3 853 635
ENST00000541352 Q9UPY3-2 760 582
ENST00000556045 A0A7I2YBM0* 34 22
ENST00000529720 Q9UPY3 1 1

Gene Properties

Type
Protein Coding
Chromosome
14
Cytoband
14q32.13
Entrez ID
Aliases
DCR1DicerDicer1eGLOWHERNAK12H4.8-LIKE

Recurrent Mutations

All 676 amino-acid changes on canonical ENST00000343455 · 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 DICER1 · 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 DICER1 – 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
8/40 20%
0/0 0%
Endometrial Carcinoma
15/42 36%
59/612 10%
Chronic Myelogenous Leukemia
2/25 8%
0/0 0%
Chordoma
0/7 0%
1/13 8%
Melanoma
11/210 5%
94/1899 5%
T-Cell Non-Hodgkins Lymphoma
1/26 4%
0/0 0%
Acute Monocytic Leukemia
0/1 0%
1/25 4%
Colorectal Carcinoma
20/143 14%
106/3239 3%
Other Solid Cancers
3/94 3%
55/1515 4%
Squamous Cell Lung Carcinoma
3/57 5%
23/810 3%
Non-Small Cell Lung Carcinoma
15/304 5%
31/1390 2%
Cervical Carcinoma
3/35 9%
9/422 2%
Thymic Epithelial Tumor
0/0 0%
1/39 3%
Bladder Carcinoma
3/58 5%
23/956 2%
Small Cell Lung Carcinoma
0/9 0%
18/752 2%
Other Sarcomas
3/69 4%
14/699 2%
Hodgkins Lymphoma
1/16 6%
2/122 2%
Ewings Sarcoma
5/63 8%
1/262 0%
Oral Cavity Carcinoma
1/54 2%
0/0 0%
Neuroendocrine Tumour
5/154 3%
8/577 1%
Plasma Cell Myeloma
0/44 0%
6/305 2%
Biliary Tract Carcinoma
4/54 7%
10/950 1%
Gastric Carcinoma
0/74 0%
26/1809 1%
Hepatocellular Carcinoma
1/46 2%
26/2210 1%
Glioma
0/52 0%
26/2127 1%
Breast Carcinoma
3/144 2%
36/3264 1%
Esophageal Carcinoma
0/23 0%
9/769 1%
Thyroid Gland Carcinoma
1/45 2%
17/1592 1%
Esophageal Squamous Cell Carcinoma
2/51 4%
26/2550 1%
Wilms Tumour
0/5 0%
5/474 1%

Mutation Distribution

Where DICER1 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in DICER1 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 4,304 mutations in DICER1

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