BMP7

Bone morphogenetic protein 7 P18075 BMP7_HUMAN
Protein Coding Chr 20 20q13.31 Swiss-Prot reviewed Entrez 655
Mutations
967
CL 136 · Tissue 822
Samples
371
CL 72 · Tissue 294
Peptides
275
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
Mutations967136822
Samples37172294
Peptides27556226

Function

BMP7 · Bone morphogenetic protein 7

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 each subunit of the disulfide-linked homodimer, which plays a role in bone, kidney and brown adipose tissue development. Additionally, this protein induces ectopic bone formation and may promote fracture healing in human patients. [provided by RefSeq, Jul 2016].

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
ENST00000395863 P18075 384 243
ENST00000450594 B1AL00* 321 216
ENST00000395864 B1AKZ9* 262 174

Gene Properties

Type
Protein Coding
Chromosome
20
Cytoband
20q13.31
Entrez ID
Aliases
OP-1

Recurrent Mutations

All 243 amino-acid changes on canonical ENST00000395863 · 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 BMP7 · 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 BMP7 – 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
Burkitts Lymphoma
1/32 3%
12/196 6%
Endometrial Carcinoma
6/42 14%
28/612 5%
T-Cell Non-Hodgkins Lymphoma
1/26 4%
0/0 0%
Non-Small Cell Lung Carcinoma
12/304 4%
24/1390 2%
Oral Cavity Carcinoma
1/54 2%
0/0 0%
Melanoma
6/210 3%
32/1899 2%
Gastric Carcinoma
3/74 4%
28/1809 2%
Colorectal Carcinoma
7/143 5%
35/3239 1%
Glioblastoma
1/98 1%
0/0 0%
Squamous Cell Lung Carcinoma
4/57 7%
4/810 0%
Adrenocortical Carcinoma
0/3 0%
1/112 1%
Hepatocellular Carcinoma
0/46 0%
19/2210 1%
Neuroendocrine Tumour
1/154 1%
5/577 1%
B-Cell Non-Hodgkins Lymphoma
5/88 6%
13/2534 1%
Small Cell Lung Carcinoma
0/9 0%
5/752 1%
Cervical Carcinoma
0/35 0%
3/422 1%
Ovarian Carcinoma
1/109 1%
6/998 1%
Ewings Sarcoma
0/63 0%
2/262 1%
Bladder Carcinoma
2/58 3%
4/956 0%
Plasma Cell Myeloma
2/44 5%
0/305 0%
Germ Cell Tumour
0/25 0%
1/169 1%
Biliary Tract Carcinoma
1/54 2%
4/950 0%
Thyroid Gland Carcinoma
0/45 0%
8/1592 0%
Pancreatic Carcinoma
2/89 2%
6/1611 0%
Kidney Carcinoma
3/85 4%
6/1862 0%
Non-Cancerous
1/104 1%
3/830 0%
Prostate Carcinoma
0/13 0%
9/2105 0%
Neuroblastoma
2/87 2%
4/1331 0%
Other Sarcomas
2/69 3%
1/699 0%
Other Solid Cancers
1/94 1%
5/1515 0%

Mutation Distribution

Where BMP7 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in BMP7 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 967 mutations in BMP7

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