CCNG2

Cyclin G2 Q16589 CCNG2_HUMAN
Protein Coding Chr 4 4q21.1 Swiss-Prot reviewed Entrez 901
Mutations
368
CL 84 · Tissue 284
Samples
102
CL 31 · Tissue 71
Peptides
85
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
Mutations36884284
Samples1023171
Peptides851870

Function

CCNG2 · Cyclin G2

The eukaryotic cell cycle is governed by cyclin-dependent protein kinases (CDKs) whose activities are regulated by cyclins and CDK inhibitors. The 8 species of cyclins reported in mammals, cyclins A through H, share a conserved amino acid sequence of about 90 residues called the cyclin box. The amino acid sequence of cyclin G is well conserved among mammals. The nucleotide sequence of cyclin G1 and cyclin G2 are 53% identical. Unlike cyclin G1, cyclin G2 contains a C-terminal PEST protein destabilization motif, suggesting that cyclin G2 expression is tightly regulated through the cell cycle. [provided by RefSeq, Jul 2008].

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
ENST00000316355 Q16589 104 84
ENST00000395640 Q16589 91 82
ENST00000502280 Q16589 91 82
ENST00000509972 Q16589-2 82 73

Gene Properties

Type
Protein Coding
Chromosome
4
Cytoband
4q21.1
Entrez ID

Recurrent Mutations

All 84 amino-acid changes on canonical ENST00000316355 · 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 CCNG2 · 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 CCNG2 – 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
1/40 2%
0/0 0%
Osteosarcoma
2/45 4%
0/166 0%
Cervical Carcinoma
3/35 9%
1/422 0%
Endometrial Carcinoma
0/42 0%
5/612 1%
Hodgkins Lymphoma
0/16 0%
1/122 1%
Bladder Carcinoma
0/58 0%
7/956 1%
Melanoma
6/210 3%
6/1899 0%
Non-Small Cell Lung Carcinoma
7/304 2%
2/1390 0%
Colorectal Carcinoma
5/143 4%
12/3239 0%
Burkitts Lymphoma
0/32 0%
1/196 1%
Gastric Carcinoma
2/74 3%
5/1809 0%
Plasma Cell Myeloma
0/44 0%
1/305 0%
Neuroendocrine Tumour
0/154 0%
2/577 0%
Esophageal Carcinoma
0/23 0%
2/769 0%
Head and Neck Carcinoma
1/85 1%
3/1574 0%
Squamous Cell Lung Carcinoma
0/57 0%
2/810 0%
Biliary Tract Carcinoma
0/54 0%
2/950 0%
Ovarian Carcinoma
0/109 0%
2/998 0%
Kidney Carcinoma
0/85 0%
3/1862 0%
Prostate Carcinoma
1/13 8%
2/2105 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
3/2550 0%
Hepatocellular Carcinoma
0/46 0%
2/2210 0%
Glioma
0/52 0%
2/2127 0%
Breast Carcinoma
0/144 0%
3/3264 0%
B-Cell Non-Hodgkins Lymphoma
0/88 0%
2/2534 0%
B-Lymphoblastic Leukemia
2/55 4%
0/2640 0%
Pancreatic Carcinoma
1/89 1%
0/1611 0%

Mutation Distribution

Where CCNG2 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in CCNG2 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 368 mutations in CCNG2

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