CAMK2G

Calcium/calmodulin dependent protein kinase II gamma Q13555-4 KCC2G_HUMAN
Protein Coding Chr 10 10q22.2 Swiss-Prot reviewed Entrez 818
Mutations
1,293
CL 117 · Tissue 1,160
Samples
218
CL 34 · Tissue 180
Peptides
211
unique mutant peptides
Transcripts
8
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
Mutations1,2931171,160
Samples21834180
Peptides21133178

Function

CAMK2G · Calcium/calmodulin dependent protein kinase II gamma

The product of this gene is one of the four subunits of an enzyme which belongs to the serine/threonine protein kinase family, and to the Ca(2+)/calmodulin-dependent protein kinase subfamily. Calcium signaling is crucial for several aspects of plasticity at glutamatergic synapses. In mammalian cells the enzyme is composed of four different chains: alpha, beta, gamma, and delta. The product of this gene is a gamma chain. Many alternatively spliced transcripts encoding different isoforms have been described but the full-length nature of all the variants has not been determined.[provided by RefSeq, Mar 2011].

Isoforms & Proteins

8 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
ENST00000322680 A0A2Q3DQE3* 205 151
ENST00000305762 Q13555-4 194 145
ENST00000680035 Q13555-11 191 141
ENST00000322635 Q13555-5 189 140
ENST00000372765 Q5SWX3* 181 135
ENST00000351293 Q13555-10 177 132
ENST00000423381 H0Y6G2* 147 104
ENST00000394762 A0A804CJ50* 9 6

Gene Properties

Type
Protein Coding
Chromosome
10
Cytoband
10q22.2
Entrez ID
Aliases
CAMKCAMK-IICAMKGMRD59

Recurrent Mutations

All 145 amino-acid changes on canonical ENST00000305762 · 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 CAMK2G · 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 CAMK2G – 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
2/25 8%
0/0 0%
T-Lymphoblastic Leukemia
3/40 8%
0/0 0%
T-Cell Non-Hodgkins Lymphoma
1/26 4%
0/0 0%
Endometrial Carcinoma
3/42 7%
13/612 2%
Melanoma
3/210 1%
26/1899 1%
Gastric Carcinoma
2/74 3%
17/1809 1%
Thyroid Gland Carcinoma
0/45 0%
15/1592 1%
Colorectal Carcinoma
4/143 3%
26/3239 1%
Bladder Carcinoma
0/58 0%
8/956 1%
Cervical Carcinoma
0/35 0%
3/422 1%
Neuroendocrine Tumour
4/154 3%
0/577 0%
Non-Cancerous
0/104 0%
5/830 1%
Rhabdomyosarcoma
0/33 0%
1/171 1%
Non-Small Cell Lung Carcinoma
2/304 1%
5/1390 0%
Glioma
0/52 0%
9/2127 0%
Other Sarcomas
2/69 3%
1/699 0%
Head and Neck Carcinoma
1/85 1%
4/1574 0%
Hepatocellular Carcinoma
0/46 0%
6/2210 0%
Small Cell Lung Carcinoma
0/9 0%
2/752 0%
Other Solid Cancers
0/94 0%
4/1515 0%
Pancreatic Carcinoma
0/89 0%
4/1611 0%
Squamous Cell Lung Carcinoma
0/57 0%
2/810 0%
Medulloblastoma
0/0 0%
1/450 0%
Neuroblastoma
2/87 2%
1/1331 0%
Breast Carcinoma
1/144 1%
6/3264 0%
Prostate Carcinoma
2/13 15%
2/2105 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
5/2550 0%
B-Cell Non-Hodgkins Lymphoma
0/88 0%
5/2534 0%
Ovarian Carcinoma
1/109 1%
1/998 0%
B-Lymphoblastic Leukemia
1/55 2%
3/2640 0%

Mutation Distribution

Where CAMK2G is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in CAMK2G 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 1,293 mutations in CAMK2G

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