TAC4

Tachykinin precursor 4 Q86UU9 TKN4_HUMAN
Protein Coding Chr 17 17q21.33 Swiss-Prot reviewed Entrez 255061
Mutations
258
CL 61 · Tissue 197
Samples
56
CL 9 · Tissue 47
Peptides
85
unique mutant peptides
Transcripts
5
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
Mutations25861197
Samples56947
Peptides852074

Function

TAC4 · Tachykinin precursor 4

This gene is a member of the tachykinin family of neurotransmitter-encoding genes. Tachykinin proteins are cleaved into small, secreted peptides that activate members of a family of receptor proteins. The products of this gene preferentially activate tachykinin receptor 1, and are thought to regulate peripheral endocrine and paracrine functions including blood pressure, the immune system, and endocrine gland secretion. The products of this gene lack a dibasic cleavage site found in other tachykinin proteins. Consequently, the nature of the cleavage products generated in vivo remains to be determined. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008].

Isoforms & Proteins

5 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
ENST00000334568 Q86UU9 60 41
ENST00000436235 Q86UU9-5 59 39
ENST00000326219 Q86UU9-3 49 31
ENST00000398154 Q86UU9-2 49 32
ENST00000352793 Q86UU9-4 41 25

Gene Properties

Type
Protein Coding
Chromosome
17
Cytoband
17q21.33
Entrez ID
Aliases
EKHK-1PPT-C

Recurrent Mutations

All 41 amino-acid changes on canonical ENST00000334568 · 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 TAC4 · 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 TAC4 – 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
Oral Cavity Carcinoma
2/54 4%
0/0 0%
Endometrial Carcinoma
0/42 0%
5/612 1%
Osteosarcoma
1/45 2%
0/166 0%
Other Solid Cancers
0/94 0%
5/1515 0%
Plasma Cell Myeloma
0/44 0%
1/305 0%
Melanoma
0/210 0%
6/1899 0%
Squamous Cell Lung Carcinoma
0/57 0%
2/810 0%
Cervical Carcinoma
0/35 0%
1/422 0%
Colorectal Carcinoma
0/143 0%
6/3239 0%
Gastric Carcinoma
0/74 0%
3/1809 0%
Hepatocellular Carcinoma
1/46 2%
2/2210 0%
Other Sarcomas
1/69 1%
0/699 0%
Thyroid Gland Carcinoma
0/45 0%
2/1592 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
3/2550 0%
Non-Small Cell Lung Carcinoma
0/304 0%
2/1390 0%
B-Cell Non-Hodgkins Lymphoma
2/88 2%
1/2534 0%
Non-Cancerous
0/104 0%
1/830 0%
Biliary Tract Carcinoma
0/54 0%
1/950 0%
Bladder Carcinoma
0/58 0%
1/956 0%
Breast Carcinoma
1/144 1%
2/3264 0%
Glioma
0/52 0%
2/2127 0%
Head and Neck Carcinoma
1/85 1%
0/1574 0%
Kidney Carcinoma
0/85 0%
1/1862 0%

Mutation Distribution

Where TAC4 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in TAC4 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 48 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 258 mutations in TAC4

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