CDC23

Cell division cycle 23 Q9UJX2 CDC23_HUMAN
Protein Coding Chr 5 5q31.2 Swiss-Prot reviewed Entrez 8697
Mutations
341
CL 46 · Tissue 288
Samples
244
CL 41 · Tissue 197
Peptides
199
unique mutant peptides
Transcripts
3
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
Mutations34146288
Samples24441197
Peptides19928168

Function

CDC23 · Cell division cycle 23

The protein encoded by this gene shares strong similarity with Saccharomyces cerevisiae Cdc23, a protein essential for cell cycle progression through the G2/M transition. This protein is a component of anaphase-promoting complex (APC), which is composed of eight protein subunits and highly conserved in eukaryotic cells. APC catalyzes the formation of cyclin B-ubiquitin conjugate that is responsible for the ubiquitin-mediated proteolysis of B-type cyclins. This protein and 3 other members of the APC complex contain the TPR (tetratricopeptide repeat), a protein domain important for protein-protein interaction. [provided by RefSeq, Jul 2008].

Isoforms & Proteins

3 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
ENST00000394886 Q9UJX2 238 169
ENST00000394884 Q9UJX2-2 57 51
ENST00000505120 D6RCF8* 46 44

Gene Properties

Type
Protein Coding
Chromosome
5
Cytoband
5q31.2
Entrez ID
Aliases
ANAPC8APC8CUT23

Recurrent Mutations

All 169 amino-acid changes on canonical ENST00000394886 · 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 CDC23 · 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 CDC23 – 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-Cell Non-Hodgkins Lymphoma
3/26 12%
0/0 0%
T-Lymphoblastic Leukemia
1/40 2%
0/0 0%
Acute Myeloid Leukemia
2/90 2%
0/0 0%
Glioblastoma
2/98 2%
0/0 0%
Endometrial Carcinoma
2/42 5%
11/612 2%
Hodgkins Lymphoma
2/16 12%
0/122 0%
Melanoma
0/210 0%
28/1899 1%
Colorectal Carcinoma
5/143 4%
33/3239 1%
Other Solid Cancers
2/94 2%
13/1515 1%
Gastric Carcinoma
3/74 4%
14/1809 1%
Pancreatic Carcinoma
4/89 4%
10/1611 1%
Bladder Carcinoma
0/58 0%
8/956 1%
Squamous Cell Lung Carcinoma
0/57 0%
5/810 1%
Non-Small Cell Lung Carcinoma
2/304 1%
7/1390 0%
Thyroid Gland Carcinoma
0/45 0%
8/1592 0%
Burkitts Lymphoma
0/32 0%
1/196 1%
Glioma
0/52 0%
9/2127 0%
Other Sarcomas
2/69 3%
1/699 0%
Esophageal Squamous Cell Carcinoma
4/51 8%
6/2550 0%
Ovarian Carcinoma
2/109 2%
2/998 0%
Biliary Tract Carcinoma
0/54 0%
3/950 0%
Head and Neck Carcinoma
0/85 0%
5/1574 0%
Hepatocellular Carcinoma
0/46 0%
6/2210 0%
Small Cell Lung Carcinoma
2/9 22%
0/752 0%
Prostate Carcinoma
1/13 8%
4/2105 0%
Medulloblastoma
0/0 0%
1/450 0%
Cervical Carcinoma
0/35 0%
1/422 0%
Non-Cancerous
0/104 0%
2/830 0%
Breast Carcinoma
0/144 0%
7/3264 0%
Neuroblastoma
1/87 1%
2/1331 0%

Mutation Distribution

Where CDC23 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in CDC23 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 341 mutations in CDC23

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