KLK3

Kallikrein related peptidase 3 P07288 KLK3_HUMAN
Protein Coding Chr 19 19q13.33 Swiss-Prot reviewed Entrez 354
Mutations
830
CL 142 · Tissue 680
Samples
230
CL 53 · Tissue 173
Peptides
189
unique mutant peptides
Transcripts
5
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
Mutations830142680
Samples23053173
Peptides18949148

Function

KLK3 · Kallikrein related peptidase 3

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. The gene is one of the fifteen kallikrein subfamily members located in a cluster on chromosome 19. It encodes a single-chain glycoprotein, a protease which is synthesized in the epithelial cells of the prostate gland, and is present in seminal plasma. It is thought to function normally in the liquefaction of seminal coagulum, presumably by hydrolysis of the high molecular mass seminal vesicle protein. The serum level of this protein, called PSA in the clinical setting, is useful in the diagnosis and monitoring of prostatic carcinoma. Alternate splicing of this gene generates several transcript variants encoding different isoforms. [provided by RefSeq, Dec 2019].

Isoforms & Proteins

5 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
ENST00000326003 P07288 223 142
ENST00000595952 P07288-3 168 112
ENST00000360617 P07288-2 161 119
ENST00000593997 P07288-5 143 106
ENST00000597483 M0R294* 135 99

Gene Properties

Type
Protein Coding
Chromosome
19
Cytoband
19q13.33
Entrez ID
Aliases
APSKLK2A1PSAhK3

Recurrent Mutations

All 142 amino-acid changes on canonical ENST00000326003 · 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 KLK3 · 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 KLK3 – 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
Acute Myeloid Leukemia
5/90 6%
0/0 0%
Melanoma
4/210 2%
38/1899 2%
Rhabdomyosarcoma
0/33 0%
4/171 2%
Squamous Cell Lung Carcinoma
2/57 4%
9/810 1%
Endometrial Carcinoma
2/42 5%
5/612 1%
Non-Small Cell Lung Carcinoma
7/304 2%
9/1390 1%
Burkitts Lymphoma
2/32 6%
0/196 0%
Small Cell Lung Carcinoma
0/9 0%
6/752 1%
Other Sarcomas
4/69 6%
2/699 0%
Colorectal Carcinoma
7/143 5%
17/3239 1%
Gastric Carcinoma
2/74 3%
11/1809 1%
Head and Neck Carcinoma
0/85 0%
11/1574 1%
Non-Cancerous
1/104 1%
5/830 1%
Ewings Sarcoma
2/63 3%
0/262 0%
Germ Cell Tumour
1/25 4%
0/169 0%
Ovarian Carcinoma
2/109 2%
3/998 0%
Other Solid Cancers
2/94 2%
5/1515 0%
Cervical Carcinoma
0/35 0%
2/422 0%
Hepatocellular Carcinoma
0/46 0%
9/2210 0%
Thyroid Gland Carcinoma
0/45 0%
6/1592 0%
Glioma
1/52 2%
7/2127 0%
Prostate Carcinoma
2/13 15%
5/2105 0%
Kidney Carcinoma
0/85 0%
6/1862 0%
Plasma Cell Myeloma
0/44 0%
1/305 0%
Neuroendocrine Tumour
2/154 1%
0/577 0%
Neuroblastoma
3/87 3%
0/1331 0%
Bladder Carcinoma
0/58 0%
2/956 0%
Esophageal Squamous Cell Carcinoma
1/51 2%
4/2550 0%
Breast Carcinoma
0/144 0%
6/3264 0%
Esophageal Carcinoma
0/23 0%
1/769 0%

Mutation Distribution

Where KLK3 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in KLK3 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 50 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 830 mutations in KLK3

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