COQ10B

Coenzyme Q10B Q9H8M1 CQ10B_HUMAN
Protein Coding Chr 2 2q33.1 Swiss-Prot reviewed Entrez 80219
Mutations
191
CL 45 · Tissue 146
Samples
80
CL 24 · Tissue 56
Peptides
70
unique mutant peptides
Transcripts
3
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
Mutations19145146
Samples802456
Peptides701854

Function

COQ10B · Coenzyme Q10B

Predicted to enable ubiquinone binding activity. Predicted to be involved in cellular respiration and ubiquinone biosynthetic process. Predicted to be located in mitochondrial inner membrane. Predicted to be active in mitochondrion. [provided by Alliance of Genome Resources, Apr 2022]

Isoforms & Proteins

3 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
ENST00000263960 Q9H8M1 81 61
ENST00000409010 B8ZZV9* 57 47
ENST00000409398 B8ZZX2* 53 44

Gene Properties

Type
Protein Coding
Chromosome
2
Cytoband
2q33.1
Entrez ID

Recurrent Mutations

All 61 amino-acid changes on canonical ENST00000263960 · 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 COQ10B · 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 COQ10B – 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
2/40 5%
0/0 0%
T-Cell Non-Hodgkins Lymphoma
1/26 4%
0/0 0%
Oral Cavity Carcinoma
1/54 2%
0/0 0%
Endometrial Carcinoma
1/42 2%
7/612 1%
Plasma Cell Myeloma
2/44 5%
1/305 0%
Gastrointestinal Stromal Tumour
0/0 0%
1/133 1%
Non-Small Cell Lung Carcinoma
6/304 2%
5/1390 0%
Squamous Cell Lung Carcinoma
2/57 4%
2/810 0%
Colorectal Carcinoma
4/143 3%
11/3239 0%
Bladder Carcinoma
0/58 0%
4/956 0%
Meningioma
1/3 33%
0/252 0%
Melanoma
1/210 0%
4/1899 0%
Non-Cancerous
0/104 0%
2/830 0%
Gastric Carcinoma
2/74 3%
2/1809 0%
Other Solid Cancers
0/94 0%
3/1515 0%
Hepatocellular Carcinoma
0/46 0%
3/2210 0%
Breast Carcinoma
0/144 0%
4/3264 0%
Glioma
0/52 0%
2/2127 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
2/2550 0%
Head and Neck Carcinoma
0/85 0%
1/1574 0%
Kidney Carcinoma
0/85 0%
1/1862 0%
B-Cell Non-Hodgkins Lymphoma
0/88 0%
1/2534 0%
B-Lymphoblastic Leukemia
1/55 2%
0/2640 0%

Mutation Distribution

Where COQ10B is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in COQ10B 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 191 mutations in COQ10B

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