CDC6

Cell division cycle 6 Q99741 CDC6_HUMAN
Protein Coding Chr 17 17q21.2 Swiss-Prot reviewed Entrez 990
Mutations
232
CL 44 · Tissue 183
Samples
221
CL 43 · Tissue 174
Peptides
166
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
Mutations23244183
Samples22143174
Peptides16620146

Function

CDC6 · Cell division cycle 6

The protein encoded by this gene is highly similar to Saccharomyces cerevisiae Cdc6, a protein essential for the initiation of DNA replication. This protein functions as a regulator at the early steps of DNA replication. It localizes in cell nucleus during cell cyle G1, but translocates to the cytoplasm at the start of S phase. The subcellular translocation of this protein during cell cyle is regulated through its phosphorylation by Cdks. Transcription of this protein was reported to be regulated in response to mitogenic signals through transcriptional control mechanism involving E2F proteins. [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
ENST00000209728 Q99741 232 166

Gene Properties

Type
Protein Coding
Chromosome
17
Cytoband
17q21.2
Entrez ID
Aliases
CDC18LHsCDC18HsCDC6MGORS5

Recurrent Mutations

All 166 amino-acid changes on canonical ENST00000209728 · 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 CDC6 · 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 CDC6 – 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
4/40 10%
0/0 0%
Rhabdomyosarcoma
0/33 0%
4/171 2%
Endometrial Carcinoma
0/42 0%
11/612 2%
Gastrointestinal Stromal Tumour
0/0 0%
2/133 2%
Bladder Carcinoma
0/58 0%
15/956 2%
Squamous Cell Lung Carcinoma
2/57 4%
9/810 1%
Acute Myeloid Leukemia
1/90 1%
0/0 0%
Gastric Carcinoma
0/74 0%
20/1809 1%
Glioblastoma
1/98 1%
0/0 0%
Non-Small Cell Lung Carcinoma
6/304 2%
10/1390 1%
Cervical Carcinoma
0/35 0%
4/422 1%
Burkitts Lymphoma
0/32 0%
2/196 1%
Esophageal Squamous Cell Carcinoma
2/51 4%
15/2550 1%
Melanoma
2/210 1%
11/1899 1%
Germ Cell Tumour
0/25 0%
1/169 1%
Colorectal Carcinoma
5/143 4%
12/3239 0%
Osteosarcoma
1/45 2%
0/166 0%
Ovarian Carcinoma
1/109 1%
4/998 0%
Mesothelioma
1/62 2%
0/165 0%
Head and Neck Carcinoma
3/85 4%
4/1574 0%
Neuroendocrine Tumour
2/154 1%
1/577 0%
Biliary Tract Carcinoma
1/54 2%
3/950 0%
Esophageal Carcinoma
1/23 4%
2/769 0%
Other Solid Cancers
1/94 1%
5/1515 0%
Ewings Sarcoma
0/63 0%
1/262 0%
Hepatocellular Carcinoma
0/46 0%
7/2210 0%
B-Lymphoblastic Leukemia
3/55 5%
5/2640 0%
Plasma Cell Myeloma
0/44 0%
1/305 0%
Breast Carcinoma
0/144 0%
10/3264 0%
B-Cell Non-Hodgkins Lymphoma
0/88 0%
7/2534 0%

Mutation Distribution

Where CDC6 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in CDC6 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 232 mutations in CDC6

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