KLK15

Kallikrein related peptidase 15 Q9H2R5 KLK15_HUMAN
Protein Coding Chr 19 19q13.33 Swiss-Prot reviewed Entrez 55554
Mutations
809
CL 111 · Tissue 692
Samples
306
CL 60 · Tissue 244
Peptides
206
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
Mutations809111692
Samples30660244
Peptides20636181

Function

KLK15 · Kallikrein related peptidase 15

Kallikreins are a subgroup of serine proteases having diverse physiological functions. Growing evidence suggests that many kallikreins are implicated in carcinogenesis and some have potential as novel cancer and other disease biomarkers. This gene is one of the fifteen kallikrein subfamily members located in a cluster on chromosome 19. In prostate cancer, this gene has increased expression, which indicates its possible use as a diagnostic or prognostic marker for prostate cancer. The gene contains multiple polyadenylation sites and alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2008].

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
ENST00000598239 Q9H2R5 318 183
ENST00000326856 Q9H2R5-5 285 172
ENST00000596931 M0R0D7* 206 120

Gene Properties

Type
Protein Coding
Chromosome
19
Cytoband
19q13.33
Entrez ID
Aliases
ACOHSRNASPH

Recurrent Mutations

All 183 amino-acid changes on canonical ENST00000598239 · 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 KLK15 · 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 KLK15 – 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
2/54 4%
0/0 0%
Melanoma
3/210 1%
48/1899 3%
Acute Myeloid Leukemia
2/90 2%
0/0 0%
Non-Small Cell Lung Carcinoma
18/304 6%
19/1390 1%
Endometrial Carcinoma
3/42 7%
9/612 1%
Hodgkins Lymphoma
2/16 12%
0/122 0%
Squamous Cell Lung Carcinoma
1/57 2%
11/810 1%
Gastric Carcinoma
1/74 1%
21/1809 1%
Colorectal Carcinoma
3/143 2%
36/3239 1%
Other Solid Cancers
1/94 1%
16/1515 1%
Meningioma
1/3 33%
1/252 0%
Bladder Carcinoma
0/58 0%
7/956 1%
Cervical Carcinoma
0/35 0%
3/422 1%
Esophageal Carcinoma
0/23 0%
5/769 1%
Glioma
2/52 4%
11/2127 1%
Non-Cancerous
0/104 0%
4/830 0%
Breast Carcinoma
6/144 4%
8/3264 0%
Biliary Tract Carcinoma
1/54 2%
3/950 0%
Small Cell Lung Carcinoma
0/9 0%
3/752 0%
Head and Neck Carcinoma
1/85 1%
5/1574 0%
Hepatocellular Carcinoma
0/46 0%
8/2210 0%
Pancreatic Carcinoma
0/89 0%
6/1611 0%
B-Lymphoblastic Leukemia
8/55 15%
1/2640 0%
Ewings Sarcoma
0/63 0%
1/262 0%
Plasma Cell Myeloma
0/44 0%
1/305 0%
Neuroendocrine Tumour
2/154 1%
0/577 0%
Prostate Carcinoma
0/13 0%
5/2105 0%
Esophageal Squamous Cell Carcinoma
1/51 2%
5/2550 0%
Neuroblastoma
2/87 2%
1/1331 0%
Thyroid Gland Carcinoma
0/45 0%
2/1592 0%

Mutation Distribution

Where KLK15 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in KLK15 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 14 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 809 mutations in KLK15

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