CAMK2D

Calcium/calmodulin dependent protein kinase II delta Q13557 KCC2D_HUMAN
Protein Coding Chr 4 4q26 Swiss-Prot reviewed Entrez 817
Mutations
1,858
CL 203 · Tissue 1,650
Samples
221
CL 41 · Tissue 176
Peptides
220
unique mutant peptides
Transcripts
11
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
Mutations1,8582031,650
Samples22141176
Peptides22028188

Function

CAMK2D · Calcium/calmodulin dependent protein kinase II delta

The product of this gene 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 delta chain. Alternative splicing results in multiple transcript variants encoding distinct isoforms. Distinct isoforms of this chain have different expression patterns.[provided by RefSeq, Nov 2008].

Isoforms & Proteins

11 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
ENST00000511664 E9PF82* 211 168
ENST00000515496 Q13557-3 189 161
ENST00000342666 Q13557 186 159
ENST00000514328 D6R938* 186 159
ENST00000394522 Q13557-10 183 155
ENST00000508738 Q13557-9 182 154
ENST00000505990 E9PBG7* 181 153
ENST00000296402 Q13557-8 179 152
ENST00000379773 Q13557-8 179 152
ENST00000394524 Q13557-12 179 152
ENST00000683023 Q13557 3 3

Gene Properties

Type
Protein Coding
Chromosome
4
Cytoband
4q26
Entrez ID
Aliases
CAMKD

Recurrent Mutations

All 161 amino-acid changes on canonical ENST00000515496 · 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 CAMK2D · 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 CAMK2D – 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%
Acute Myeloid Leukemia
5/90 6%
0/0 0%
Chordoma
0/7 0%
1/13 8%
Glioblastoma
3/98 3%
0/0 0%
Endometrial Carcinoma
1/42 2%
13/612 2%
Oral Cavity Carcinoma
1/54 2%
0/0 0%
Non-Small Cell Lung Carcinoma
5/304 2%
16/1390 1%
Melanoma
0/210 0%
21/1899 1%
Bladder Carcinoma
4/58 7%
6/956 1%
Gastric Carcinoma
3/74 4%
12/1809 1%
Meningioma
0/3 0%
2/252 1%
Colorectal Carcinoma
5/143 4%
21/3239 1%
Thyroid Gland Carcinoma
0/45 0%
12/1592 1%
Hodgkins Lymphoma
0/16 0%
1/122 1%
Other Solid Cancers
2/94 2%
8/1515 1%
Plasma Cell Myeloma
0/44 0%
2/305 1%
Biliary Tract Carcinoma
0/54 0%
5/950 1%
Cervical Carcinoma
0/35 0%
2/422 0%
Neuroendocrine Tumour
1/154 1%
2/577 0%
Ovarian Carcinoma
0/109 0%
4/998 0%
Squamous Cell Lung Carcinoma
0/57 0%
3/810 0%
Glioma
0/52 0%
7/2127 0%
Kidney Carcinoma
2/85 2%
4/1862 0%
Head and Neck Carcinoma
1/85 1%
4/1574 0%
Prostate Carcinoma
0/13 0%
6/2105 0%
B-Cell Non-Hodgkins Lymphoma
1/88 1%
6/2534 0%
Other Sarcomas
0/69 0%
2/699 0%
Hepatocellular Carcinoma
0/46 0%
5/2210 0%
Pancreatic Carcinoma
0/89 0%
3/1611 0%
Breast Carcinoma
1/144 1%
4/3264 0%

Mutation Distribution

Where CAMK2D is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in CAMK2D 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 1,858 mutations in CAMK2D

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