CDK9

Cyclin dependent kinase 9 P50750 CDK9_HUMAN
Protein Coding Chr 9 9q34.11 Swiss-Prot reviewed Entrez 1025
Mutations
188
CL 49 · Tissue 135
Samples
184
CL 47 · Tissue 133
Peptides
135
unique mutant peptides
Transcripts
1
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
Mutations18849135
Samples18447133
Peptides13529110

Function

CDK9 · Cyclin dependent kinase 9

The protein encoded by this gene is a member of the cyclin-dependent protein kinase (CDK) family. CDK family members are highly similar to the gene products of S. cerevisiae cdc28, and S. pombe cdc2, and known as important cell cycle regulators. This kinase was found to be a component of the multiprotein complex TAK/P-TEFb, which is an elongation factor for RNA polymerase II-directed transcription and functions by phosphorylating the C-terminal domain of the largest subunit of RNA polymerase II. This protein forms a complex with and is regulated by its regulatory subunit cyclin T or cyclin K. HIV-1 Tat protein was found to interact with this protein and cyclin T, which suggested a possible involvement of this protein in AIDS. [provided by RefSeq, Jul 2008].

Isoforms & Proteins

1 transcript · 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
ENST00000373264 P50750 188 135

Gene Properties

Type
Protein Coding
Chromosome
9
Cytoband
9q34.11
Entrez ID
Aliases
C-2kCDC2L4CTK1PITALRETAK

Recurrent Mutations

All 135 amino-acid changes on canonical ENST00000373264 · 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 CDK9 · 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 CDK9 – 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%
Chronic Myelogenous Leukemia
2/25 8%
0/0 0%
Endometrial Carcinoma
0/42 0%
8/612 1%
Plasma Cell Myeloma
0/44 0%
4/305 1%
Melanoma
2/210 1%
19/1899 1%
Non-Small Cell Lung Carcinoma
10/304 3%
7/1390 0%
Bladder Carcinoma
2/58 3%
8/956 1%
Cervical Carcinoma
1/35 3%
3/422 1%
Burkitts Lymphoma
1/32 3%
1/196 1%
Colorectal Carcinoma
5/143 4%
24/3239 1%
Hodgkins Lymphoma
0/16 0%
1/122 1%
Gastric Carcinoma
0/74 0%
11/1809 1%
Neuroendocrine Tumour
2/154 1%
2/577 0%
Germ Cell Tumour
0/25 0%
1/169 1%
Medulloblastoma
0/0 0%
2/450 0%
Hepatocellular Carcinoma
0/46 0%
10/2210 0%
Other Solid Cancers
0/94 0%
6/1515 0%
Squamous Cell Lung Carcinoma
2/57 4%
1/810 0%
Ewings Sarcoma
0/63 0%
1/262 0%
Ovarian Carcinoma
2/109 2%
1/998 0%
Other Sarcomas
1/69 1%
1/699 0%
Head and Neck Carcinoma
1/85 1%
3/1574 0%
Glioma
0/52 0%
5/2127 0%
Non-Cancerous
0/104 0%
2/830 0%
Pancreatic Carcinoma
0/89 0%
3/1611 0%
B-Cell Non-Hodgkins Lymphoma
3/88 3%
1/2534 0%
Prostate Carcinoma
2/13 15%
1/2105 0%
Small Cell Lung Carcinoma
0/9 0%
1/752 0%
Breast Carcinoma
1/144 1%
3/3264 0%
Esophageal Squamous Cell Carcinoma
1/51 2%
2/2550 0%

Mutation Distribution

Where CDK9 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in CDK9 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 188 mutations in CDK9

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