CDKN3

Cyclin dependent kinase inhibitor 3 Q16667 CDKN3_HUMAN
Protein Coding Chr 14 14q22.2 Swiss-Prot reviewed Entrez 1033
Mutations
333
CL 32 · Tissue 299
Samples
69
CL 14 · Tissue 54
Peptides
69
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
Mutations33332299
Samples691454
Peptides69958

Function

CDKN3 · Cyclin dependent kinase inhibitor 3

The protein encoded by this gene belongs to the dual specificity protein phosphatase family. It was identified as a cyclin-dependent kinase inhibitor, and has been shown to interact with, and dephosphorylate CDK2 kinase, thus prevent the activation of CDK2 kinase. This gene was reported to be deleted, mutated, or overexpressed in several kinds of cancers. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2008].

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
ENST00000335183 Q16667 70 50
ENST00000458126 H7C0S3* 56 44
ENST00000556102 G3V2J7* 45 37
ENST00000442975 Q16667-2 42 35
ENST00000395577 F8WD24* 41 34
ENST00000543789 G3V1K6* 40 32
ENST00000541304 F5H232* 39 31

Gene Properties

Type
Protein Coding
Chromosome
14
Cytoband
14q22.2
Entrez ID
Aliases
CDI1CIP2KAPKAP1

Recurrent Mutations

All 50 amino-acid changes on canonical ENST00000335183 · 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 CDKN3 · 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 CDKN3 – 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
Chronic Myelogenous Leukemia
1/25 4%
0/0 0%
Oral Cavity Carcinoma
1/54 2%
0/0 0%
Gastrointestinal Stromal Tumour
0/0 0%
2/133 2%
Germ Cell Tumour
1/25 4%
1/169 1%
Endometrial Carcinoma
1/42 2%
5/612 1%
Colorectal Carcinoma
6/143 4%
4/3239 0%
Glioma
0/52 0%
6/2127 0%
Other Solid Cancers
1/94 1%
3/1515 0%
Gastric Carcinoma
0/74 0%
4/1809 0%
Non-Small Cell Lung Carcinoma
1/304 0%
2/1390 0%
Head and Neck Carcinoma
1/85 1%
2/1574 0%
B-Cell Non-Hodgkins Lymphoma
0/88 0%
4/2534 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
4/2550 0%
Prostate Carcinoma
0/13 0%
3/2105 0%
Neuroendocrine Tumour
0/154 0%
1/577 0%
Hepatocellular Carcinoma
0/46 0%
3/2210 0%
Esophageal Carcinoma
0/23 0%
1/769 0%
Other Sarcomas
0/69 0%
1/699 0%
Thyroid Gland Carcinoma
0/45 0%
2/1592 0%
Breast Carcinoma
1/144 1%
3/3264 0%
Bladder Carcinoma
0/58 0%
1/956 0%
Melanoma
0/210 0%
2/1899 0%
Kidney Carcinoma
0/85 0%
1/1862 0%

Mutation Distribution

Where CDKN3 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in CDKN3 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 333 mutations in CDKN3

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