TCP11

T-complex 11 Q8WWU5 TCP11_HUMAN
Protein Coding Chr 6 6p21.31 Swiss-Prot reviewed Entrez 6954
Mutations
1,716
CL 205 · Tissue 1,486
Samples
239
CL 47 · Tissue 188
Peptides
230
unique mutant peptides
Transcripts
10
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
Mutations1,7162051,486
Samples23947188
Peptides23037197

Function

TCP11 · T-complex 11

Predicted to be involved in several processes, including protein kinase A signaling; regulation of cAMP-mediated signaling; and regulation of sperm capacitation. Located in acrosomal vesicle and sperm flagellum. [provided by Alliance of Genome Resources, Apr 2022]

Isoforms & Proteins

10 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
ENST00000673754 Q8WWU5-7 226 157
ENST00000512012 Q8WWU5 224 155
ENST00000373974 Q8WWU5-4 209 145
ENST00000244645 Q8WWU5-2 208 137
ENST00000412155 Q8WWU5-6 204 142
ENST00000418521 Q8WWU5-3 200 138
ENST00000611141 Q8WWU5-3 198 136
ENST00000373979 Q8WWU5-2 193 131
ENST00000311875 Q8WWU5 43 37
ENST00000444780 A0A6E1WXZ9* 11 8

Gene Properties

Type
Protein Coding
Chromosome
6
Cytoband
6p21.31
Entrez ID
Aliases
D6S230EFPPR

Recurrent Mutations

All 155 amino-acid changes on canonical ENST00000512012 · 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 TCP11 · 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 TCP11 – 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
5/40 12%
0/0 0%
Oral Cavity Carcinoma
2/54 4%
0/0 0%
Endometrial Carcinoma
5/42 12%
16/612 3%
Glioblastoma
3/98 3%
0/0 0%
Melanoma
4/210 2%
52/1899 3%
Acute Myeloid Leukemia
2/90 2%
0/0 0%
Gastrointestinal Stromal Tumour
0/0 0%
2/133 2%
Other Solid Cancers
0/94 0%
17/1515 1%
Squamous Cell Lung Carcinoma
1/57 2%
7/810 1%
Colorectal Carcinoma
7/143 5%
23/3239 1%
Mesothelioma
2/62 3%
0/165 0%
Adrenocortical Carcinoma
0/3 0%
1/112 1%
Plasma Cell Myeloma
1/44 2%
2/305 1%
Ovarian Carcinoma
1/109 1%
7/998 1%
Gastric Carcinoma
0/74 0%
12/1809 1%
Esophageal Carcinoma
1/23 4%
3/769 0%
Bladder Carcinoma
1/58 2%
4/956 0%
Non-Small Cell Lung Carcinoma
1/304 0%
7/1390 0%
Cervical Carcinoma
0/35 0%
2/422 0%
Pancreatic Carcinoma
3/89 3%
4/1611 0%
Ewings Sarcoma
0/63 0%
1/262 0%
Other Sarcomas
1/69 1%
1/699 0%
Head and Neck Carcinoma
1/85 1%
3/1574 0%
Non-Cancerous
2/104 2%
0/830 0%
Kidney Carcinoma
0/85 0%
4/1862 0%
Breast Carcinoma
2/144 1%
3/3264 0%
Neuroblastoma
1/87 1%
1/1331 0%
Glioma
0/52 0%
3/2127 0%
Neuroendocrine Tumour
1/154 1%
0/577 0%
Small Cell Lung Carcinoma
0/9 0%
1/752 0%

Mutation Distribution

Where TCP11 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in TCP11 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 1,716 mutations in TCP11

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