TOP6BL

TOP6B like initiator of meiotic double strand breaks Q8N6T0 TO6BL_HUMAN
Protein Coding Chr 11 11q13.2 Swiss-Prot reviewed Entrez 79703
Mutations
32
CL 18 · Tissue 0
Samples
24
CL 18 · Tissue 0
Peptides
32
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
Mutations32180
Samples24180
Peptides32180

Function

TOP6BL · TOP6B like initiator of meiotic double strand breaks

Predicted to be involved in meiotic DNA double-strand break formation and reciprocal meiotic recombination. Predicted to be located in chromosome. Implicated in gestational trophoblastic neoplasm. [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
ENST00000540737 Q8N6T0 18 18
ENST00000525908 A0A2U3TZP7* 11 11
ENST00000524551 E9PMI8* 3 3

Gene Properties

Type
Protein Coding
Chromosome
11
Cytoband
11q13.2
Entrez ID
Aliases
C11orf80HYDM4TOPOVIBL

Recurrent Mutations

All 18 amino-acid changes on canonical ENST00000540737 · 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 TOP6BL · 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 TOP6BL – 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
Glioblastoma
1/98 1%
0/0 0%
Endometrial Carcinoma
4/42 10%
1/612 0%
Hodgkins Lymphoma
1/16 6%
0/122 0%
Meningioma
1/3 33%
0/252 0%
Ewings Sarcoma
1/63 2%
0/262 0%
Gastric Carcinoma
2/74 3%
1/1809 0%
Non-Small Cell Lung Carcinoma
1/304 0%
1/1390 0%
Biliary Tract Carcinoma
1/54 2%
0/950 0%
Bladder Carcinoma
0/58 0%
1/956 0%
Colorectal Carcinoma
3/143 2%
0/3239 0%
Neuroblastoma
1/87 1%
0/1331 0%
Pancreatic Carcinoma
1/89 1%
0/1611 0%
Melanoma
0/210 0%
1/1899 0%
Glioma
0/52 0%
1/2127 0%
Other Blood Cancers
1/61 2%
0/2725 0%

Mutation Distribution

Where TOP6BL is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in TOP6BL 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.

Mutations

All 32 mutations in TOP6BL

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