TLR10

Toll like receptor 10 Q9BXR5 TLR10_HUMAN
Protein Coding Chr 4 4p14 Swiss-Prot reviewed Entrez 81793
Mutations
2,404
CL 250 · Tissue 2,154
Samples
356
CL 65 · Tissue 291
Peptides
278
unique mutant peptides
Transcripts
6
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
Mutations2,4042502,154
Samples35665291
Peptides27841244

Function

TLR10 · Toll like receptor 10

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 most highly expressed in lymphoid tissues such as spleen, lymph node, thymus, and tonsil. Multiple alternatively spliced transcript variants which encode different protein isoforms have been found for this gene. [provided by RefSeq, Aug 2010].

Isoforms & Proteins

6 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
ENST00000308973 Q9BXR5 429 278
ENST00000361424 Q9BXR5 395 272
ENST00000506111 Q9BXR5 395 272
ENST00000508334 Q9BXR5 395 272
ENST00000613579 Q9BXR5 395 272
ENST00000622002 Q9BXR5 395 272

Gene Properties

Type
Protein Coding
Chromosome
4
Cytoband
4p14
Entrez ID
Aliases
CD290

Recurrent Mutations

All 278 amino-acid changes on canonical ENST00000308973 · 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 TLR10 · 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 TLR10 – 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%
Chronic Myelogenous Leukemia
2/25 8%
0/0 0%
Endometrial Carcinoma
3/42 7%
25/612 4%
Acute Myeloid Leukemia
3/90 3%
0/0 0%
Gastrointestinal Stromal Tumour
0/0 0%
4/133 3%
Melanoma
4/210 2%
57/1899 3%
Non-Small Cell Lung Carcinoma
10/304 3%
24/1390 2%
Other Solid Cancers
2/94 2%
20/1515 1%
Colorectal Carcinoma
8/143 6%
35/3239 1%
Bladder Carcinoma
0/58 0%
12/956 1%
Neuroendocrine Tumour
5/154 3%
3/577 1%
Cervical Carcinoma
0/35 0%
4/422 1%
Adrenocortical Carcinoma
0/3 0%
1/112 1%
Gastric Carcinoma
4/74 5%
12/1809 1%
Ovarian Carcinoma
5/109 5%
3/998 0%
Hepatocellular Carcinoma
0/46 0%
15/2210 1%
Non-Cancerous
1/104 1%
5/830 1%
Biliary Tract Carcinoma
0/54 0%
5/950 1%
Rhabdomyosarcoma
0/33 0%
1/171 1%
Squamous Cell Lung Carcinoma
2/57 4%
2/810 0%
Head and Neck Carcinoma
0/85 0%
7/1574 0%
Glioma
0/52 0%
9/2127 0%
Prostate Carcinoma
0/13 0%
8/2105 0%
Pancreatic Carcinoma
2/89 2%
4/1611 0%
B-Cell Non-Hodgkins Lymphoma
3/88 3%
6/2534 0%
Kidney Carcinoma
2/85 2%
4/1862 0%
Other Sarcomas
0/69 0%
2/699 0%
Breast Carcinoma
4/144 3%
5/3264 0%
Other Blood Cancers
0/61 0%
7/2725 0%
Medulloblastoma
0/0 0%
1/450 0%

Mutation Distribution

Where TLR10 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in TLR10 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 2,404 mutations in TLR10

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