DEFB136

Defensin beta 136 Q30KP8 DB136_HUMAN
Protein Coding Chr 8 8p23.1 Swiss-Prot reviewed Entrez 613210
Mutations
67
CL 18 · Tissue 48
Samples
67
CL 18 · Tissue 48
Peptides
40
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
Mutations671848
Samples671848
Peptides40933

Function

DEFB136 · Defensin beta 136

Defensins are cysteine-rich cationic polypeptides that are important in the immunologic response to invading microorganisms. The antimicrobial protein encoded by this gene is secreted and is a member of the beta defensin protein family. Beta defensin genes are found in several clusters throughout the genome, with this gene mapping to a cluster at 8p23. [provided by RefSeq, Nov 2014].

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
ENST00000382209 Q30KP8 67 40

Gene Properties

Type
Protein Coding
Chromosome
8
Cytoband
8p23.1
Entrez ID
Aliases
DEFB137

Recurrent Mutations

All 40 amino-acid changes on canonical ENST00000382209 · 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 DEFB136 · 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 DEFB136 – 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
Oral Cavity Carcinoma
1/54 2%
0/0 0%
Endometrial Carcinoma
3/42 7%
3/612 0%
Neuroendocrine Tumour
4/154 3%
2/577 0%
Gastrointestinal Stromal Tumour
0/0 0%
1/133 1%
Colorectal Carcinoma
2/143 1%
12/3239 0%
Non-Small Cell Lung Carcinoma
6/304 2%
0/1390 0%
Melanoma
0/210 0%
7/1899 0%
Gastric Carcinoma
0/74 0%
6/1809 0%
Other Solid Cancers
0/94 0%
5/1515 0%
Squamous Cell Lung Carcinoma
0/57 0%
2/810 0%
Biliary Tract Carcinoma
0/54 0%
2/950 0%
Small Cell Lung Carcinoma
0/9 0%
1/752 0%
Esophageal Carcinoma
0/23 0%
1/769 0%
Other Sarcomas
0/69 0%
1/699 0%
Head and Neck Carcinoma
1/85 1%
1/1574 0%
Bladder Carcinoma
0/58 0%
1/956 0%
Thyroid Gland Carcinoma
1/45 2%
0/1592 0%
Breast Carcinoma
0/144 0%
2/3264 0%
Pancreatic Carcinoma
0/89 0%
1/1611 0%
Kidney Carcinoma
0/85 0%
1/1862 0%

Mutation Distribution

Where DEFB136 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in DEFB136 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 67 mutations in DEFB136

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