DCLK3

Doublecortin like kinase 3 Q9C098 DCLK3_HUMAN
Protein Coding Chr 3 3p22.2 Swiss-Prot reviewed Entrez 85443
Mutations
1,007
CL 144 · Tissue 851
Samples
510
CL 94 · Tissue 412
Peptides
378
unique mutant peptides
Transcripts
2
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
Mutations1,007144851
Samples51094412
Peptides37867322

Function

DCLK3 · Doublecortin like kinase 3

Predicted to enable protein kinase activity. Predicted to be involved in peptidyl-serine phosphorylation. Predicted to act upstream of or within negative regulation of protein localization to nucleus. Predicted to be active in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Apr 2022]

Isoforms & Proteins

2 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
ENST00000636136 A0A1B0GTZ4* 541 374
ENST00000416516 Q9C098 466 336

Gene Properties

Type
Protein Coding
Chromosome
3
Cytoband
3p22.2
Entrez ID
Aliases
CLRDCAMKL3DCDC3CDCK3

Recurrent Mutations

All 336 amino-acid changes on canonical ENST00000416516 · 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 DCLK3 · 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 DCLK3 – 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
5/40 12%
0/0 0%
Endometrial Carcinoma
11/42 26%
25/612 4%
Melanoma
8/210 4%
87/1899 5%
Chronic Myelogenous Leukemia
1/25 4%
0/0 0%
Non-Small Cell Lung Carcinoma
17/304 6%
27/1390 2%
Unknown
1/10 10%
0/29 0%
Colorectal Carcinoma
14/143 10%
64/3239 2%
Other Solid Cancers
4/94 4%
27/1515 2%
Squamous Cell Lung Carcinoma
5/57 9%
10/810 1%
Gastric Carcinoma
2/74 3%
30/1809 2%
Hodgkins Lymphoma
2/16 12%
0/122 0%
Cervical Carcinoma
2/35 6%
3/422 1%
Small Cell Lung Carcinoma
0/9 0%
8/752 1%
Other Sarcomas
4/69 6%
4/699 1%
Glioblastoma
1/98 1%
0/0 0%
Thyroid Gland Carcinoma
1/45 2%
13/1592 1%
Plasma Cell Myeloma
1/44 2%
2/305 1%
Non-Cancerous
0/104 0%
8/830 1%
Esophageal Carcinoma
2/23 9%
4/769 1%
Gastrointestinal Stromal Tumour
0/0 0%
1/133 1%
Biliary Tract Carcinoma
0/54 0%
7/950 1%
Glioma
0/52 0%
14/2127 1%
Ovarian Carcinoma
1/109 1%
6/998 1%
Hepatocellular Carcinoma
1/46 2%
13/2210 1%
Prostate Carcinoma
1/13 8%
10/2105 0%
Germ Cell Tumour
0/25 0%
1/169 1%
Osteosarcoma
1/45 2%
0/166 0%
Neuroendocrine Tumour
0/154 0%
3/577 1%
Pancreatic Carcinoma
0/89 0%
7/1611 0%
Bladder Carcinoma
0/58 0%
4/956 0%

Mutation Distribution

Where DCLK3 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in DCLK3 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 1,007 mutations in DCLK3

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