TLR5

Toll like receptor 5 O60602 TLR5_HUMAN
Protein Coding Chr 1 1q41 Swiss-Prot reviewed Entrez 7100
Mutations
943
CL 162 · Tissue 764
Samples
459
CL 98 · Tissue 353
Peptides
345
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
Mutations943162764
Samples45998353
Peptides34559287

Function

TLR5 · Toll like receptor 5

This gene encodes a member of the toll-like receptor (TLR) family, which plays a fundamental role in pathogen recognition and activation of innate immune responses. These receptors recognize distinct pathogen-associated molecular patterns that are expressed on infectious agents. The protein encoded by this gene recognizes bacterial flagellin, the principal component of bacterial flagella and a virulence factor. The activation of this receptor mobilizes the nuclear factor NF-kappaB, which in turn activates a host of inflammatory-related target genes. Mutations in this gene have been associated with both resistance and susceptibility to systemic lupus erythematosus, and susceptibility to Legionnaire disease.[provided by RefSeq, Dec 2009].

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
ENST00000642603 O60602 499 344
ENST00000540964 O60602 443 326
ENST00000407096 B1AZ06* 1 1

Gene Properties

Type
Protein Coding
Chromosome
1
Cytoband
1q41
Entrez ID
Aliases
MELIOSSLE1SLEB1TIL3

Recurrent Mutations

All 344 amino-acid changes on canonical ENST00000642603 · 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 TLR5 · 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 TLR5 – 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
10/40 25%
0/0 0%
Endometrial Carcinoma
4/42 10%
29/612 5%
Melanoma
10/210 5%
76/1899 4%
T-Cell Non-Hodgkins Lymphoma
1/26 4%
0/0 0%
Oral Cavity Carcinoma
1/54 2%
0/0 0%
Colorectal Carcinoma
8/143 6%
52/3239 2%
Non-Small Cell Lung Carcinoma
12/304 4%
17/1390 1%
Squamous Cell Lung Carcinoma
6/57 11%
8/810 1%
Gastrointestinal Stromal Tumour
0/0 0%
2/133 2%
Gastric Carcinoma
1/74 1%
26/1809 1%
Other Sarcomas
3/69 4%
8/699 1%
Bladder Carcinoma
0/58 0%
14/956 1%
Other Solid Cancers
4/94 4%
17/1515 1%
Plasma Cell Myeloma
1/44 2%
3/305 1%
Cervical Carcinoma
2/35 6%
3/422 1%
Small Cell Lung Carcinoma
0/9 0%
8/752 1%
Germ Cell Tumour
0/25 0%
2/169 1%
Neuroendocrine Tumour
6/154 4%
1/577 0%
Ovarian Carcinoma
6/109 6%
4/998 0%
Esophageal Carcinoma
0/23 0%
7/769 1%
Burkitts Lymphoma
2/32 6%
0/196 0%
Non-Cancerous
0/104 0%
7/830 1%
Ewings Sarcoma
1/63 2%
1/262 0%
Hepatocellular Carcinoma
3/46 7%
9/2210 0%
Biliary Tract Carcinoma
2/54 4%
3/950 0%
Breast Carcinoma
3/144 2%
14/3264 0%
Rhabdomyosarcoma
0/33 0%
1/171 1%
Head and Neck Carcinoma
1/85 1%
7/1574 0%
Kidney Carcinoma
4/85 5%
5/1862 0%
Meningioma
0/3 0%
1/252 0%

Mutation Distribution

Where TLR5 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in TLR5 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 943 mutations in TLR5

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