CDK5

Cyclin dependent kinase 5 Q00535 CDK5_HUMAN
Protein Coding Chr 7 7q36.1 Swiss-Prot reviewed Entrez 1020
Mutations
265
CL 31 · Tissue 231
Samples
137
CL 19 · Tissue 115
Peptides
108
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
Mutations26531231
Samples13719115
Peptides1081789

Function

CDK5 · Cyclin dependent kinase 5

This gene encodes a proline-directed serine/threonine kinase that is a member of the cyclin-dependent kinase family of proteins. Unlike other members of the family, the protein encoded by this gene does not directly control cell cycle regulation. Instead the protein, which is predominantly expressed at high levels in mammalian postmitotic central nervous system neurons, functions in diverse processes such as synaptic plasticity and neuronal migration through phosphorylation of proteins required for cytoskeletal organization, endocytosis and exocytosis, and apoptosis. In humans, an allelic variant of the gene that results in undetectable levels of the protein has been associated with lethal autosomal recessive lissencephaly-7. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2015].

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
ENST00000485972 Q00535 146 100
ENST00000297518 Q00535-2 119 82

Gene Properties

Type
Protein Coding
Chromosome
7
Cytoband
7q36.1
Entrez ID
Aliases
LIS7PSSALRE

Recurrent Mutations

All 100 amino-acid changes on canonical ENST00000485972 · 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 CDK5 · 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 CDK5 – 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%
15/612 2%
Acute Myeloid Leukemia
1/90 1%
0/0 0%
Melanoma
1/210 0%
17/1899 1%
Colorectal Carcinoma
5/143 4%
21/3239 1%
Prostate Carcinoma
0/13 0%
13/2105 1%
Osteosarcoma
1/45 2%
0/166 0%
Gastric Carcinoma
0/74 0%
8/1809 0%
Neuroendocrine Tumour
0/154 0%
3/577 1%
Biliary Tract Carcinoma
0/54 0%
4/950 0%
Other Sarcomas
1/69 1%
2/699 0%
Other Solid Cancers
1/94 1%
5/1515 0%
Bladder Carcinoma
0/58 0%
3/956 0%
Head and Neck Carcinoma
0/85 0%
5/1574 0%
Non-Small Cell Lung Carcinoma
0/304 0%
5/1390 0%
Squamous Cell Lung Carcinoma
0/57 0%
2/810 0%
Glioma
1/52 2%
3/2127 0%
Esophageal Carcinoma
0/23 0%
1/769 0%
Small Cell Lung Carcinoma
0/9 0%
1/752 0%
Breast Carcinoma
0/144 0%
4/3264 0%
Non-Cancerous
0/104 0%
1/830 0%
Ovarian Carcinoma
0/109 0%
1/998 0%
B-Cell Non-Hodgkins Lymphoma
0/88 0%
2/2534 0%
Pancreatic Carcinoma
1/89 1%
0/1611 0%
Kidney Carcinoma
1/85 1%
0/1862 0%
B-Lymphoblastic Leukemia
0/55 0%
1/2640 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
1/2550 0%

Mutation Distribution

Where CDK5 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in CDK5 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 265 mutations in CDK5

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