DGKB

Diacylglycerol kinase beta Q9Y6T7 DGKB_HUMAN
Protein Coding Chr 7 7p21.2 Swiss-Prot reviewed Entrez 1607
Mutations
3,686
CL 538 · Tissue 3,123
Samples
732
CL 147 · Tissue 581
Peptides
552
unique mutant peptides
Transcripts
5
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
Mutations3,6865383,123
Samples732147581
Peptides552107475

Function

DGKB · Diacylglycerol kinase beta

Diacylglycerol kinases (DGKs) are regulators of the intracellular concentration of the second messenger diacylglycerol (DAG) and thus play a key role in cellular processes. Nine mammalian isotypes have been identified, which are encoded by separate genes. Mammalian DGK isozymes contain a conserved catalytic (kinase) domain and a cysteine-rich domain (CRD). The protein encoded by this gene is a diacylglycerol kinase, beta isotype. Several alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2017].

Isoforms & Proteins

5 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
ENST00000402815 B5MBY2* 809 513
ENST00000399322 Q9Y6T7 729 497
ENST00000403951 Q9Y6T7 729 497
ENST00000407950 B5MCD5* 724 493
ENST00000406247 Q9Y6T7-2 695 474

Gene Properties

Type
Protein Coding
Chromosome
7
Cytoband
7p21.2
Entrez ID
Aliases
DAGK2DGKDGK-BETA

Recurrent Mutations

All 497 amino-acid changes on canonical ENST00000399322 · 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 DGKB · 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 DGKB – 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
4/40 10%
0/0 0%
Hodgkins Lymphoma
2/16 12%
6/122 5%
Endometrial Carcinoma
6/42 14%
31/612 5%
Oral Cavity Carcinoma
3/54 6%
0/0 0%
Melanoma
20/210 10%
94/1899 5%
Non-Small Cell Lung Carcinoma
29/304 10%
52/1390 4%
Other Solid Cancers
2/94 2%
55/1515 4%
Squamous Cell Lung Carcinoma
6/57 11%
24/810 3%
Glioblastoma
3/98 3%
0/0 0%
Colorectal Carcinoma
22/143 15%
58/3239 2%
Acute Myeloid Leukemia
2/90 2%
0/0 0%
Gastric Carcinoma
5/74 7%
36/1809 2%
Ovarian Carcinoma
3/109 3%
21/998 2%
Small Cell Lung Carcinoma
0/9 0%
16/752 2%
Neuroendocrine Tumour
10/154 6%
3/577 1%
Plasma Cell Myeloma
3/44 7%
3/305 1%
Bladder Carcinoma
3/58 5%
13/956 1%
Gastrointestinal Stromal Tumour
0/0 0%
2/133 2%
Rhabdomyosarcoma
1/33 3%
2/171 1%
Esophageal Squamous Cell Carcinoma
1/51 2%
30/2550 1%
Chondrosarcoma
0/14 0%
1/75 1%
Head and Neck Carcinoma
2/85 2%
15/1574 1%
Esophageal Carcinoma
2/23 9%
5/769 1%
Non-Cancerous
0/104 0%
8/830 1%
Other Sarcomas
0/69 0%
6/699 1%
Hepatocellular Carcinoma
0/46 0%
16/2210 1%
Prostate Carcinoma
0/13 0%
15/2105 1%
Thyroid Gland Carcinoma
1/45 2%
10/1592 1%
Breast Carcinoma
5/144 3%
18/3264 1%

Mutation Distribution

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

Mutation counts by tissue
Mutation Distribution

How many mutations in DGKB 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 53 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 3,686 mutations in DGKB

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