TIFA

TRAF interacting protein with forkhead associated domain Q96CG3 TIFA_HUMAN
Protein Coding Chr 4 4q25 Swiss-Prot reviewed Entrez 92610
Mutations
120
CL 20 · Tissue 100
Samples
62
CL 13 · Tissue 49
Peptides
50
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
Mutations12020100
Samples621349
Peptides50842

Function

TIFA · TRAF interacting protein with forkhead associated domain

This gene encodes an adapter protein involved in adaptive and innate immunity. This protein includes a forkhead-associated (FHA) domain that specifically binds to phosphorylated serine and threonine residues. In response to bacterial infection, the encoded host cell protein undergoes an intermolecular interaction between the FHA domain and a phosphorylated threonine that leads to protein oligomerization and stimulation of the NF-kappa B and other downstream signaling pathways. This protein exhibits reduced expression in hepatocellular carcinoma and may suppress hepatocellular carcinoma progression. This protein may also play a role in the DNA damage response. [provided by RefSeq, Jun 2018].

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
ENST00000361717 Q96CG3 63 50
ENST00000500655 Q96CG3 57 49

Gene Properties

Type
Protein Coding
Chromosome
4
Cytoband
4q25
Entrez ID
Aliases
T2BPT6BPTIFAA

Recurrent Mutations

All 50 amino-acid changes on canonical ENST00000361717 · 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 TIFA · 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 TIFA – 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
Endometrial Carcinoma
2/42 5%
3/612 0%
Other Sarcomas
0/69 0%
3/699 0%
Melanoma
3/210 1%
4/1899 0%
Colorectal Carcinoma
3/143 2%
7/3239 0%
Gastric Carcinoma
0/74 0%
5/1809 0%
Other Solid Cancers
0/94 0%
4/1515 0%
Non-Cancerous
0/104 0%
2/830 0%
Bladder Carcinoma
0/58 0%
2/956 0%
Breast Carcinoma
0/144 0%
5/3264 0%
Esophageal Squamous Cell Carcinoma
2/51 4%
2/2550 0%
Glioma
0/52 0%
3/2127 0%
Neuroendocrine Tumour
0/154 0%
1/577 0%
Neuroblastoma
2/87 2%
0/1331 0%
Small Cell Lung Carcinoma
0/9 0%
1/752 0%
Thyroid Gland Carcinoma
0/45 0%
2/1592 0%
Head and Neck Carcinoma
0/85 0%
2/1574 0%
Prostate Carcinoma
0/13 0%
2/2105 0%
Non-Small Cell Lung Carcinoma
1/304 0%
0/1390 0%
Kidney Carcinoma
0/85 0%
1/1862 0%

Mutation Distribution

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

Mutation counts by tissue
Mutation Distribution

How many mutations in TIFA 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 120 mutations in TIFA

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