KBTBD12

Kelch repeat and BTB domain containing 12 Q3ZCT8 KBTBC_HUMAN
Protein Coding Chr 3 3q21.3 Swiss-Prot reviewed Entrez 166348
Mutations
950
CL 143 · Tissue 787
Samples
360
CL 67 · Tissue 283
Peptides
259
unique mutant peptides
Transcripts
4
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
Mutations950143787
Samples36067283
Peptides25946219

Isoforms & Proteins

4 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
ENST00000405109 Q3ZCT8 371 242
ENST00000405256 Q3ZCT8 337 230
ENST00000407609 B5MCZ4* 122 86
ENST00000343941 Q3ZCT8-2 120 76

Gene Properties

Type
Protein Coding
Chromosome
3
Cytoband
3q21.3
Entrez ID
Aliases
KLHDC6

Recurrent Mutations

All 242 amino-acid changes on canonical ENST00000405109 · 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 KBTBD12 · 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 KBTBD12 – 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
Melanoma
7/210 3%
68/1899 4%
Endometrial Carcinoma
4/42 10%
16/612 3%
Gastrointestinal Stromal Tumour
0/0 0%
3/133 2%
Osteosarcoma
3/45 7%
1/166 1%
Oral Cavity Carcinoma
1/54 2%
0/0 0%
Rhabdomyosarcoma
2/33 6%
1/171 1%
Colorectal Carcinoma
15/143 10%
34/3239 1%
Squamous Cell Lung Carcinoma
2/57 4%
10/810 1%
Other Solid Cancers
3/94 3%
19/1515 1%
Other Sarcomas
0/69 0%
8/699 1%
Non-Small Cell Lung Carcinoma
6/304 2%
9/1390 1%
Cervical Carcinoma
0/35 0%
4/422 1%
Adrenocortical Carcinoma
1/3 33%
0/112 0%
Esophageal Squamous Cell Carcinoma
5/51 10%
16/2550 1%
Non-Cancerous
0/104 0%
7/830 1%
Ovarian Carcinoma
7/109 6%
1/998 0%
Bladder Carcinoma
1/58 2%
6/956 1%
Gastric Carcinoma
0/74 0%
12/1809 1%
Ewings Sarcoma
0/63 0%
2/262 1%
Head and Neck Carcinoma
0/85 0%
10/1574 1%
Small Cell Lung Carcinoma
0/9 0%
4/752 1%
Hepatocellular Carcinoma
0/46 0%
12/2210 1%
Glioma
2/52 4%
9/2127 0%
Biliary Tract Carcinoma
0/54 0%
5/950 1%
Mesothelioma
1/62 2%
0/165 0%
Esophageal Carcinoma
1/23 4%
2/769 0%
Thyroid Gland Carcinoma
0/45 0%
6/1592 0%
B-Cell Non-Hodgkins Lymphoma
1/88 1%
7/2534 0%
Plasma Cell Myeloma
0/44 0%
1/305 0%
Pancreatic Carcinoma
2/89 2%
2/1611 0%

Mutation Distribution

Where KBTBD12 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in KBTBD12 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 950 mutations in KBTBD12

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