BMP10

Bone morphogenetic protein 10 O95393 BMP10_HUMAN
Protein Coding Chr 2 2p13.3 Swiss-Prot reviewed Entrez 27302
Mutations
312
CL 55 · Tissue 257
Samples
296
CL 53 · Tissue 243
Peptides
206
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
Mutations31255257
Samples29653243
Peptides20631184

Function

BMP10 · Bone morphogenetic protein 10

This gene encodes a secreted ligand of the TGF-beta (transforming growth factor-beta) superfamily of proteins. Ligands of this family bind various TGF-beta receptors leading to recruitment and activation of SMAD family transcription factors that regulate gene expression. The encoded preproprotein is proteolytically processed to generate the mature protein, which binds to the activin receptor-like kinase 1 (ALK1) and plays important roles in cardiovascular development including cardiomyocyte proliferation and regulation of heart size, closure of the ductus arteriosus, angiogenesis and ventricular trabeculation. [provided by RefSeq, Aug 2016].

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
ENST00000295379 O95393 312 206

Gene Properties

Type
Protein Coding
Chromosome
2
Cytoband
2p13.3
Entrez ID

Recurrent Mutations

All 206 amino-acid changes on canonical ENST00000295379 · 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 BMP10 · 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 BMP10 – 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-Lymphoblastic Leukemia
7/40 18%
0/0 0%
Endometrial Carcinoma
4/42 10%
15/612 2%
Melanoma
4/210 2%
53/1899 3%
Glioblastoma
2/98 2%
0/0 0%
Other Solid Cancers
0/94 0%
21/1515 1%
Colorectal Carcinoma
6/143 4%
38/3239 1%
Squamous Cell Lung Carcinoma
0/57 0%
11/810 1%
Non-Small Cell Lung Carcinoma
8/304 3%
13/1390 1%
Neuroendocrine Tumour
5/154 3%
2/577 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
22/2550 1%
Gastric Carcinoma
2/74 3%
14/1809 1%
Gastrointestinal Stromal Tumour
0/0 0%
1/133 1%
Hodgkins Lymphoma
0/16 0%
1/122 1%
Ovarian Carcinoma
6/109 6%
2/998 0%
Bladder Carcinoma
0/58 0%
6/956 1%
Small Cell Lung Carcinoma
0/9 0%
4/752 1%
Esophageal Carcinoma
0/23 0%
4/769 1%
Mesothelioma
1/62 2%
0/165 0%
Other Sarcomas
0/69 0%
3/699 0%
Non-Cancerous
0/104 0%
3/830 0%
Breast Carcinoma
5/144 3%
5/3264 0%
Medulloblastoma
0/0 0%
1/450 0%
Biliary Tract Carcinoma
0/54 0%
2/950 0%
Thyroid Gland Carcinoma
0/45 0%
3/1592 0%
Glioma
0/52 0%
4/2127 0%
Kidney Carcinoma
1/85 1%
2/1862 0%
Prostate Carcinoma
0/13 0%
3/2105 0%
Hepatocellular Carcinoma
0/46 0%
3/2210 0%
B-Cell Non-Hodgkins Lymphoma
0/88 0%
3/2534 0%
Other Blood Cancers
1/61 2%
1/2725 0%

Mutation Distribution

Where BMP10 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in BMP10 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 15 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 312 mutations in BMP10

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