KBTBD6

Kelch repeat and BTB domain containing 6 Q86V97 KBTB6_HUMAN
Protein Coding Chr 13 13q14.11 Swiss-Prot reviewed Entrez 89890
Mutations
288
CL 37 · Tissue 243
Samples
265
CL 36 · Tissue 223
Peptides
209
unique mutant peptides
Transcripts
1
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
Mutations28837243
Samples26536223
Peptides20923186

Function

KBTBD6 · Kelch repeat and BTB domain containing 6

Involved in proteasome-mediated ubiquitin-dependent protein catabolic process; protein K48-linked ubiquitination; and regulation of Rac protein signal transduction. Located in cytoplasm and nucleus. Part of Cul3-RING ubiquitin ligase complex. [provided by Alliance of Genome Resources, Apr 2022]

Isoforms & Proteins

1 transcript · 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
ENST00000379485 Q86V97 288 209

Gene Properties

Type
Protein Coding
Chromosome
13
Cytoband
13q14.11
Entrez ID

Recurrent Mutations

All 209 amino-acid changes on canonical ENST00000379485 · 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 KBTBD6 · 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 KBTBD6 – 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
Endometrial Carcinoma
5/42 12%
24/612 4%
Colorectal Carcinoma
10/143 7%
43/3239 1%
Melanoma
1/210 0%
27/1899 1%
Squamous Cell Lung Carcinoma
3/57 5%
7/810 1%
Non-Small Cell Lung Carcinoma
4/304 1%
15/1390 1%
Germ Cell Tumour
0/25 0%
2/169 1%
Rhabdomyosarcoma
0/33 0%
2/171 1%
Ovarian Carcinoma
1/109 1%
7/998 1%
Biliary Tract Carcinoma
0/54 0%
7/950 1%
Gastric Carcinoma
0/74 0%
13/1809 1%
Non-Cancerous
0/104 0%
6/830 1%
Other Solid Cancers
2/94 2%
8/1515 1%
Bladder Carcinoma
0/58 0%
6/956 1%
Plasma Cell Myeloma
2/44 5%
0/305 0%
Hepatocellular Carcinoma
0/46 0%
12/2210 1%
Head and Neck Carcinoma
2/85 2%
6/1574 0%
Osteosarcoma
1/45 2%
0/166 0%
Kidney Carcinoma
2/85 2%
6/1862 0%
Neuroendocrine Tumour
1/154 1%
2/577 0%
Glioma
0/52 0%
8/2127 0%
Other Sarcomas
1/69 1%
1/699 0%
Prostate Carcinoma
0/13 0%
5/2105 0%
Breast Carcinoma
0/144 0%
8/3264 0%
Cervical Carcinoma
0/35 0%
1/422 0%
B-Cell Non-Hodgkins Lymphoma
0/88 0%
5/2534 0%
Small Cell Lung Carcinoma
0/9 0%
1/752 0%
Esophageal Carcinoma
0/23 0%
1/769 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
2/2550 0%
B-Lymphoblastic Leukemia
0/55 0%
2/2640 0%
Other Blood Cancers
1/61 2%
1/2725 0%

Mutation Distribution

Where KBTBD6 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in KBTBD6 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 288 mutations in KBTBD6

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