TLR1

Toll like receptor 1 Q15399 TLR1_HUMAN
Protein Coding Chr 4 4p14 Swiss-Prot reviewed Entrez 7096
Mutations
749
CL 143 · Tissue 598
Samples
359
CL 88 · Tissue 267
Peptides
281
unique mutant peptides
Transcripts
2
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
Mutations749143598
Samples35988267
Peptides28156233

Function

TLR1 · Toll like receptor 1

The protein encoded by this gene is a member of the Toll-like receptor (TLR) family which plays a fundamental role in pathogen recognition and activation of innate immunity. TLRs are highly conserved from Drosophila to humans and share structural and functional similarities. They recognize pathogen-associated molecular patterns (PAMPs) that are expressed on infectious agents, and mediate the production of cytokines necessary for the development of effective immunity. The various TLRs exhibit different patterns of expression. This gene is ubiquitously expressed, and at higher levels than other TLR genes. Different length transcripts presumably resulting from use of alternative polyadenylation site, and/or from alternative splicing, have been noted for this gene. [provided by RefSeq, Jul 2008].

Isoforms & Proteins

2 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
ENST00000308979 Q15399 397 281
ENST00000502213 Q15399 352 268

Gene Properties

Type
Protein Coding
Chromosome
4
Cytoband
4p14
Entrez ID
Aliases
CD281TILTIL. LPRS5rsc786

Recurrent Mutations

All 281 amino-acid changes on canonical ENST00000308979 · 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 TLR1 · 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 TLR1 – 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-Cell Non-Hodgkins Lymphoma
2/26 8%
0/0 0%
T-Lymphoblastic Leukemia
3/40 8%
0/0 0%
Endometrial Carcinoma
5/42 12%
21/612 3%
Gastrointestinal Stromal Tumour
0/0 0%
5/133 4%
Acute Myeloid Leukemia
2/90 2%
0/0 0%
Hodgkins Lymphoma
2/16 12%
1/122 1%
Melanoma
5/210 2%
39/1899 2%
Oral Cavity Carcinoma
1/54 2%
0/0 0%
Colorectal Carcinoma
9/143 6%
36/3239 1%
Bladder Carcinoma
1/58 2%
12/956 1%
Gastric Carcinoma
2/74 3%
19/1809 1%
Germ Cell Tumour
2/25 8%
0/169 0%
Glioblastoma
1/98 1%
0/0 0%
Non-Small Cell Lung Carcinoma
5/304 2%
12/1390 1%
Ovarian Carcinoma
5/109 5%
6/998 1%
Rhabdomyosarcoma
0/33 0%
2/171 1%
Osteosarcoma
2/45 4%
0/166 0%
Small Cell Lung Carcinoma
1/9 11%
6/752 1%
Burkitts Lymphoma
2/32 6%
0/196 0%
Neuroendocrine Tumour
4/154 3%
2/577 0%
Other Solid Cancers
2/94 2%
11/1515 1%
Esophageal Carcinoma
0/23 0%
6/769 1%
Glioma
0/52 0%
16/2127 1%
Cervical Carcinoma
0/35 0%
3/422 1%
Other Sarcomas
2/69 3%
3/699 0%
Pancreatic Carcinoma
5/89 6%
6/1611 0%
Neuroblastoma
6/87 7%
3/1331 0%
Biliary Tract Carcinoma
1/54 2%
5/950 1%
Hepatocellular Carcinoma
5/46 11%
7/2210 0%
Squamous Cell Lung Carcinoma
0/57 0%
4/810 0%

Mutation Distribution

Where TLR1 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in TLR1 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 749 mutations in TLR1

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