TADA2A

Transcriptional adaptor 2A A0A024R0Y4 A0A024R0Y4_HUMAN*
Protein Coding Chr 17 17q12 TrEMBL Entrez 6871
Mutations
33
CL 20 · Tissue 0
Samples
27
CL 20 · Tissue 0
Peptides
33
unique mutant peptides
Transcripts
1
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
Mutations33200
Samples27200
Peptides33200

Function

TADA2A · Transcriptional adaptor 2A

Many DNA-binding transcriptional activator proteins enhance the initiation rate of RNA polymerase II-mediated gene transcription by interacting functionally with the general transcription machinery bound at the basal promoter. Adaptor proteins are usually required for this activation, possibly to acetylate and destabilize nucleosomes, thereby relieving chromatin constraints at the promoter. The protein encoded by this gene is a transcriptional activator adaptor and has been found to be part of the PCAF histone acetylase complex. Several alternatively spliced transcript variants encoding different isoforms of this gene have been described, but the full-length nature of some of these variants has not been determined. [provided by RefSeq, Oct 2009].

Isoforms & Proteins

1 transcript · 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
ENST00000615182 A0A024R0Y4* 33 33

Gene Properties

Type
Protein Coding
Chromosome
17
Cytoband
17q12
Entrez ID
Aliases
ADA2ADA2AKL04PTADA2LhADA2

Recurrent Mutations

All 33 amino-acid changes on canonical ENST00000615182 · 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 TADA2A · 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 TADA2A – 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
Glioblastoma
1/98 1%
0/0 0%
Neuroendocrine Tumour
4/154 3%
0/577 0%
Endometrial Carcinoma
2/42 5%
1/612 0%
Cervical Carcinoma
0/35 0%
1/422 0%
Glioma
2/52 4%
1/2127 0%
Other Sarcomas
1/69 1%
0/699 0%
Non-Cancerous
1/104 1%
0/830 0%
Gastric Carcinoma
1/74 1%
1/1809 0%
Melanoma
1/210 0%
1/1899 0%
Colorectal Carcinoma
2/143 1%
1/3239 0%
Head and Neck Carcinoma
1/85 1%
0/1574 0%
Kidney Carcinoma
1/85 1%
0/1862 0%
B-Lymphoblastic Leukemia
1/55 2%
0/2640 0%
B-Cell Non-Hodgkins Lymphoma
1/88 1%
0/2534 0%
Hepatocellular Carcinoma
1/46 2%
0/2210 0%
Breast Carcinoma
0/144 0%
1/3264 0%

Mutation Distribution

Where TADA2A is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in TADA2A 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 33 mutations in TADA2A

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