TAC1

Tachykinin precursor 1 P20366 TKN1_HUMAN
Protein Coding Chr 7 7q21.3 Swiss-Prot reviewed Entrez 6863
Mutations
257
CL 27 · Tissue 230
Samples
94
CL 14 · Tissue 80
Peptides
107
unique mutant peptides
Transcripts
3
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
Mutations25727230
Samples941480
Peptides1071197

Function

TAC1 · Tachykinin precursor 1

This gene encodes four products of the tachykinin peptide hormone family, substance P and neurokinin A, as well as the related peptides, neuropeptide K and neuropeptide gamma. These hormones are thought to function as neurotransmitters which interact with nerve receptors and smooth muscle cells. They are known to induce behavioral responses and function as vasodilators and secretagogues. Substance P is an antimicrobial peptide with antibacterial and antifungal properties. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2014].

Isoforms & Proteins

3 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
ENST00000319273 P20366 98 77
ENST00000346867 P20366-3 80 67
ENST00000350485 P20366-2 79 65

Gene Properties

Type
Protein Coding
Chromosome
7
Cytoband
7q21.3
Entrez ID
Aliases
Hs.2563NK2NKNANPKTAC2

Recurrent Mutations

All 77 amino-acid changes on canonical ENST00000319273 · 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 TAC1 · 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 TAC1 – 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
Chondrosarcoma
0/14 0%
1/75 1%
Endometrial Carcinoma
1/42 2%
6/612 1%
Melanoma
2/210 1%
14/1899 1%
Squamous Cell Lung Carcinoma
0/57 0%
6/810 1%
Non-Small Cell Lung Carcinoma
3/304 1%
8/1390 1%
Colorectal Carcinoma
4/143 3%
9/3239 0%
Plasma Cell Myeloma
0/44 0%
1/305 0%
Glioma
0/52 0%
6/2127 0%
Neuroendocrine Tumour
1/154 1%
1/577 0%
Other Sarcomas
0/69 0%
2/699 0%
Cervical Carcinoma
0/35 0%
1/422 0%
Gastric Carcinoma
0/74 0%
4/1809 0%
Hepatocellular Carcinoma
0/46 0%
3/2210 0%
Esophageal Carcinoma
0/23 0%
1/769 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
3/2550 0%
Other Solid Cancers
0/94 0%
2/1515 0%
Head and Neck Carcinoma
0/85 0%
2/1574 0%
Thyroid Gland Carcinoma
0/45 0%
2/1592 0%
Pancreatic Carcinoma
2/89 2%
0/1611 0%
Biliary Tract Carcinoma
0/54 0%
1/950 0%
Bladder Carcinoma
0/58 0%
1/956 0%
Prostate Carcinoma
0/13 0%
2/2105 0%
Ovarian Carcinoma
1/109 1%
0/998 0%
B-Cell Non-Hodgkins Lymphoma
0/88 0%
2/2534 0%
Kidney Carcinoma
0/85 0%
1/1862 0%
Breast Carcinoma
0/144 0%
1/3264 0%

Mutation Distribution

Where TAC1 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in TAC1 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 53 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 257 mutations in TAC1

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