CDC45

Cell division cycle 45 O75419 CDC45_HUMAN
Protein Coding Chr 22 22q11.21 Swiss-Prot reviewed Entrez 8318
Mutations
784
CL 110 · Tissue 649
Samples
275
CL 57 · Tissue 213
Peptides
233
unique mutant peptides
Transcripts
4
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
Mutations784110649
Samples27557213
Peptides23339194

Function

CDC45 · Cell division cycle 45

The protein encoded by this gene was identified by its strong similarity with Saccharomyces cerevisiae Cdc45, an essential protein required to the initiation of DNA replication. Cdc45 is a member of the highly conserved multiprotein complex including Cdc6/Cdc18, the minichromosome maintenance proteins (MCMs) and DNA polymerase, which is important for early steps of DNA replication in eukaryotes. This protein has been shown to interact with MCM7 and DNA polymerase alpha. Studies of the similar gene in Xenopus suggested that this protein play a pivotal role in the loading of DNA polymerase alpha onto chromatin. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013].

Isoforms & Proteins

4 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
ENST00000263201 O75419 290 209
ENST00000437685 O75419-3 258 197
ENST00000404724 O75419-2 228 174
ENST00000407835 A0A5K1VW85* 8 6

Gene Properties

Type
Protein Coding
Chromosome
22
Cytoband
22q11.21
Entrez ID
Aliases
CDC45LCDC45L2MGORS7PORC-PI-1

Recurrent Mutations

All 209 amino-acid changes on canonical ENST00000263201 · 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 CDC45 · 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 CDC45 – 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
3/25 12%
0/0 0%
T-Lymphoblastic Leukemia
3/40 8%
0/0 0%
Chordoma
0/7 0%
1/13 8%
Acute Monocytic Leukemia
0/1 0%
1/25 4%
Endometrial Carcinoma
1/42 2%
23/612 4%
Unknown
0/10 0%
1/29 3%
Bladder Carcinoma
6/58 10%
10/956 1%
Hodgkins Lymphoma
0/16 0%
2/122 2%
Melanoma
5/210 2%
25/1899 1%
Squamous Cell Lung Carcinoma
1/57 2%
11/810 1%
Acute Myeloid Leukemia
1/90 1%
0/0 0%
Colorectal Carcinoma
7/143 5%
30/3239 1%
Cervical Carcinoma
3/35 9%
2/422 0%
Mesothelioma
2/62 3%
0/165 0%
Burkitts Lymphoma
0/32 0%
2/196 1%
Other Solid Cancers
2/94 2%
12/1515 1%
Non-Small Cell Lung Carcinoma
7/304 2%
6/1390 0%
Esophageal Carcinoma
0/23 0%
6/769 1%
Gastric Carcinoma
2/74 3%
12/1809 1%
Neuroendocrine Tumour
2/154 1%
3/577 1%
Medulloblastoma
0/0 0%
3/450 1%
Hepatocellular Carcinoma
0/46 0%
12/2210 1%
Germ Cell Tumour
0/25 0%
1/169 1%
Esophageal Squamous Cell Carcinoma
0/51 0%
13/2550 1%
Thyroid Gland Carcinoma
2/45 4%
4/1592 0%
Breast Carcinoma
0/144 0%
12/3264 0%
Prostate Carcinoma
1/13 8%
6/2105 0%
Glioma
0/52 0%
7/2127 0%
Biliary Tract Carcinoma
1/54 2%
2/950 0%
Small Cell Lung Carcinoma
0/9 0%
2/752 0%

Mutation Distribution

Where CDC45 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in CDC45 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 784 mutations in CDC45

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