BMERB1

BMERB domain containing 1 Q96MC5 MERB1_HUMAN
Protein Coding Chr 16 16p13.11 Swiss-Prot reviewed Entrez 89927
Mutations
22
CL 17 · Tissue 0
Samples
19
CL 16 · Tissue 0
Peptides
21
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
Mutations22170
Samples19160
Peptides21160

Function

BMERB1 · BMERB domain containing 1

Predicted to act upstream of or within negative regulation of cell motility involved in cerebral cortex radial glia guided migration and negative regulation of microtubule depolymerization. Predicted to be located in microtubule cytoskeleton. [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
ENST00000300006 Q96MC5 22 21

Gene Properties

Type
Protein Coding
Chromosome
16
Cytoband
16p13.11
Entrez ID
Aliases
C16orf45MINP

Recurrent Mutations

All 21 amino-acid changes on canonical ENST00000300006 · 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 BMERB1 · 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 BMERB1 – 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
Chronic Myelogenous Leukemia
1/25 4%
0/0 0%
T-Lymphoblastic Leukemia
1/40 2%
0/0 0%
Germ Cell Tumour
1/25 4%
0/169 0%
Rhabdomyosarcoma
1/33 3%
0/171 0%
Endometrial Carcinoma
0/42 0%
1/612 0%
Squamous Cell Lung Carcinoma
1/57 2%
0/810 0%
Biliary Tract Carcinoma
1/54 2%
0/950 0%
Colorectal Carcinoma
2/143 1%
1/3239 0%
Non-Small Cell Lung Carcinoma
1/304 0%
0/1390 0%
Thyroid Gland Carcinoma
1/45 2%
0/1592 0%
Pancreatic Carcinoma
1/89 1%
0/1611 0%
Kidney Carcinoma
1/85 1%
0/1862 0%
Glioma
1/52 2%
0/2127 0%
Melanoma
1/210 0%
0/1899 0%
B-Cell Non-Hodgkins Lymphoma
1/88 1%
0/2534 0%
B-Lymphoblastic Leukemia
1/55 2%
0/2640 0%
Breast Carcinoma
0/144 0%
1/3264 0%

Mutation Distribution

Where BMERB1 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in BMERB1 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 22 mutations in BMERB1

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