KLK5

Kallikrein related peptidase 5 Q9Y337 KLK5_HUMAN
Protein Coding Chr 19 19q13.41 Swiss-Prot reviewed Entrez 25818
Mutations
663
CL 80 · Tissue 579
Samples
221
CL 39 · Tissue 180
Peptides
164
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
Mutations66380579
Samples22139180
Peptides16423142

Function

KLK5 · Kallikrein related peptidase 5

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. Its expression is up-regulated by estrogens and progestins. The encoded protein is secreted and may be involved in desquamation in the epidermis. Alternative splicing results in multiple transcript variants encoding the same protein. [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
ENST00000336334 Q9Y337 235 164
ENST00000391809 Q9Y337 214 158
ENST00000593428 Q9Y337 214 158

Gene Properties

Type
Protein Coding
Chromosome
19
Cytoband
19q13.41
Entrez ID
Aliases
KLK-L2KLKL2SCTE

Recurrent Mutations

All 164 amino-acid changes on canonical ENST00000336334 · 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 KLK5 · 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 KLK5 – 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
4/40 10%
0/0 0%
Chordoma
0/7 0%
1/13 8%
Melanoma
1/210 0%
53/1899 3%
Glioblastoma
2/98 2%
0/0 0%
Osteosarcoma
3/45 7%
1/166 1%
Endometrial Carcinoma
3/42 7%
8/612 1%
Small Cell Lung Carcinoma
0/9 0%
9/752 1%
Squamous Cell Lung Carcinoma
1/57 2%
9/810 1%
Non-Small Cell Lung Carcinoma
4/304 1%
12/1390 1%
Adrenocortical Carcinoma
0/3 0%
1/112 1%
Colorectal Carcinoma
10/143 7%
15/3239 0%
Hodgkins Lymphoma
0/16 0%
1/122 1%
Germ Cell Tumour
0/25 0%
1/169 1%
Bladder Carcinoma
0/58 0%
5/956 1%
Mesothelioma
1/62 2%
0/165 0%
Burkitts Lymphoma
1/32 3%
0/196 0%
Other Solid Cancers
0/94 0%
7/1515 0%
Gastric Carcinoma
0/74 0%
8/1809 0%
Other Sarcomas
2/69 3%
1/699 0%
Hepatocellular Carcinoma
2/46 4%
5/2210 0%
Head and Neck Carcinoma
1/85 1%
4/1574 0%
Pancreatic Carcinoma
0/89 0%
5/1611 0%
Ovarian Carcinoma
0/109 0%
3/998 0%
Neuroendocrine Tumour
0/154 0%
2/577 0%
Thyroid Gland Carcinoma
0/45 0%
4/1592 0%
Cervical Carcinoma
0/35 0%
1/422 0%
Biliary Tract Carcinoma
0/54 0%
2/950 0%
Prostate Carcinoma
2/13 15%
2/2105 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
5/2550 0%
Glioma
0/52 0%
3/2127 0%

Mutation Distribution

Where KLK5 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in KLK5 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 53 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 663 mutations in KLK5

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