TLR9

Toll like receptor 9 Q9NR96 TLR9_HUMAN
Protein Coding Chr 3 3p21.2 Swiss-Prot reviewed Entrez 54106
Mutations
555
CL 106 · Tissue 426
Samples
492
CL 92 · Tissue 390
Peptides
379
unique mutant peptides
Transcripts
1
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
Mutations555106426
Samples49292390
Peptides37975304

Function

TLR9 · Toll like receptor 9

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. Studies in mice and human indicate that this receptor mediates cellular response to unmethylated CpG dinucleotides in bacterial DNA to mount an innate immune response. [provided by RefSeq, Aug 2017].

Isoforms & Proteins

1 transcript · 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
ENST00000360658 Q9NR96 555 379

Gene Properties

Type
Protein Coding
Chromosome
3
Cytoband
3p21.2
Entrez ID
Aliases
CD289

Recurrent Mutations

All 378 amino-acid changes on canonical ENST00000360658 · 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 TLR9 · 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 TLR9 – 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
9/40 22%
0/0 0%
Endometrial Carcinoma
6/42 14%
23/612 4%
Glioblastoma
4/98 4%
0/0 0%
Chronic Myelogenous Leukemia
1/25 4%
0/0 0%
Other Solid Cancers
4/94 4%
55/1515 4%
Melanoma
13/210 6%
53/1899 3%
Colorectal Carcinoma
16/143 11%
74/3239 2%
Unknown
0/10 0%
1/29 3%
Gastric Carcinoma
6/74 8%
39/1809 2%
Oral Cavity Carcinoma
1/54 2%
0/0 0%
Chondrosarcoma
0/14 0%
1/75 1%
Bladder Carcinoma
2/58 3%
8/956 1%
Rhabdomyosarcoma
0/33 0%
2/171 1%
Hepatocellular Carcinoma
1/46 2%
21/2210 1%
Non-Small Cell Lung Carcinoma
3/304 1%
13/1390 1%
Glioma
1/52 2%
17/2127 1%
Squamous Cell Lung Carcinoma
0/57 0%
7/810 1%
Pancreatic Carcinoma
1/89 1%
12/1611 1%
Esophageal Carcinoma
0/23 0%
6/769 1%
Head and Neck Carcinoma
0/85 0%
12/1574 1%
Ovarian Carcinoma
3/109 3%
5/998 0%
Hodgkins Lymphoma
0/16 0%
1/122 1%
Neuroendocrine Tumour
3/154 2%
2/577 0%
Plasma Cell Myeloma
1/44 2%
1/305 0%
Non-Cancerous
1/104 1%
4/830 0%
Germ Cell Tumour
0/25 0%
1/169 1%
Cervical Carcinoma
0/35 0%
2/422 0%
Mesothelioma
0/62 0%
1/165 1%
B-Cell Non-Hodgkins Lymphoma
4/88 5%
7/2534 0%
Other Sarcomas
0/69 0%
3/699 0%

Mutation Distribution

Where TLR9 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in TLR9 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 555 mutations in TLR9

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