TEN1

TEN1 subunit of CST complex Q86WV5 TEN1L_HUMAN
Protein Coding Chr 17 17q25.1 Swiss-Prot reviewed Entrez 100134934
Mutations
67
CL 19 · Tissue 48
Samples
47
CL 14 · Tissue 33
Peptides
33
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
Mutations671948
Samples471433
Peptides33825

Function

TEN1 · TEN1 subunit of CST complex

C17ORF106, or TEN1, appears to function in a telomere-associated complex with STN1 (OBFC1; MIM 613128) and CTC1 (C17ORF68; MIM 613129) (Miyake et al., 2009 [PubMed 19854130]).[supplied by OMIM, Nov 2009].

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
ENST00000397640 Q86WV5 44 29
ENST00000588202 K7EL09* 23 16

Gene Properties

Type
Protein Coding
Chromosome
17
Cytoband
17q25.1
Entrez ID
Aliases
C17orf106

Recurrent Mutations

All 29 amino-acid changes on canonical ENST00000397640 · 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 TEN1 · 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 TEN1 – 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
1/90 1%
0/0 0%
Hodgkins Lymphoma
0/16 0%
1/122 1%
Mesothelioma
0/62 0%
1/165 1%
Melanoma
4/210 2%
4/1899 0%
Endometrial Carcinoma
0/42 0%
2/612 0%
Esophageal Carcinoma
0/23 0%
2/769 0%
Non-Small Cell Lung Carcinoma
4/304 1%
0/1390 0%
Cervical Carcinoma
1/35 3%
0/422 0%
Colorectal Carcinoma
2/143 1%
3/3239 0%
Hepatocellular Carcinoma
0/46 0%
3/2210 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
3/2550 0%
Non-Cancerous
1/104 1%
0/830 0%
Bladder Carcinoma
0/58 0%
1/956 0%
Biliary Tract Carcinoma
0/54 0%
1/950 0%
Breast Carcinoma
0/144 0%
3/3264 0%
Prostate Carcinoma
0/13 0%
2/2105 0%
B-Lymphoblastic Leukemia
0/55 0%
2/2640 0%
Other Solid Cancers
0/94 0%
1/1515 0%
Kidney Carcinoma
0/85 0%
1/1862 0%
Glioma
0/52 0%
1/2127 0%
Gastric Carcinoma
0/74 0%
1/1809 0%
Other Blood Cancers
1/61 2%
0/2725 0%
B-Cell Non-Hodgkins Lymphoma
0/88 0%
1/2534 0%

Mutation Distribution

Where TEN1 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in TEN1 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 67 mutations in TEN1

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