NDUFB6

NADH:ubiquinone oxidoreductase subunit B6 O95139 NDUB6_HUMAN
Protein Coding Chr 9 9p21.1 Swiss-Prot reviewed Entrez 4712
Mutations
152
CL 19 · Tissue 132
Samples
61
CL 12 · Tissue 48
Peptides
68
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
Mutations15219132
Samples611248
Peptides68860

Function

NDUFB6 · NADH:ubiquinone oxidoreductase subunit B6

The protein encoded by this gene is a subunit of the multisubunit NADH:ubiquinone oxidoreductase (complex I). Mammalian complex I is composed of 45 different subunits. It locates at the mitochondrial inner membrane. This protein has NADH dehydrogenase activity and oxidoreductase activity. It transfers electrons from NADH to the respiratory chain. The immediate electron acceptor for the enzyme is believed to be ubiquinone. Alternative splicing occurs at this locus and three transcript variants encoding distinct isoforms have been identified. [provided by RefSeq, Jan 2011].

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
ENST00000379847 O95139 64 49
ENST00000350021 O95139-2 48 40
ENST00000366466 A0A087WZX2* 40 34

Gene Properties

Type
Protein Coding
Chromosome
9
Cytoband
9p21.1
Entrez ID
Aliases
B17CI

Recurrent Mutations

All 49 amino-acid changes on canonical ENST00000379847 · 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 NDUFB6 · 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 NDUFB6 – 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
1/26 4%
0/0 0%
Endometrial Carcinoma
1/42 2%
6/612 1%
Rhabdomyosarcoma
0/33 0%
1/171 1%
Non-Cancerous
1/104 1%
3/830 0%
Other Solid Cancers
2/94 2%
4/1515 0%
Neuroendocrine Tumour
2/154 1%
0/577 0%
Esophageal Carcinoma
0/23 0%
2/769 0%
Melanoma
0/210 0%
5/1899 0%
Cervical Carcinoma
0/35 0%
1/422 0%
Gastric Carcinoma
0/74 0%
4/1809 0%
Bladder Carcinoma
0/58 0%
2/956 0%
Biliary Tract Carcinoma
0/54 0%
2/950 0%
Breast Carcinoma
2/144 1%
4/3264 0%
Colorectal Carcinoma
0/143 0%
5/3239 0%
Neuroblastoma
2/87 2%
0/1331 0%
Non-Small Cell Lung Carcinoma
0/304 0%
2/1390 0%
Squamous Cell Lung Carcinoma
0/57 0%
1/810 0%
Kidney Carcinoma
1/85 1%
1/1862 0%
Ovarian Carcinoma
0/109 0%
1/998 0%
Pancreatic Carcinoma
0/89 0%
1/1611 0%
Head and Neck Carcinoma
0/85 0%
1/1574 0%
Glioma
0/52 0%
1/2127 0%
Other Blood Cancers
0/61 0%
1/2725 0%
Hepatocellular Carcinoma
0/46 0%
1/2210 0%

Mutation Distribution

Where NDUFB6 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in NDUFB6 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 152 mutations in NDUFB6

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