TAF5L

TATA-box binding protein associated factor 5 like O75529 TAF5L_HUMAN
Protein Coding Chr 1 1q42.13 Swiss-Prot reviewed Entrez 27097
Mutations
493
CL 137 · Tissue 351
Samples
309
CL 96 · Tissue 208
Peptides
239
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
Mutations493137351
Samples30996208
Peptides23958193

Function

TAF5L · TATA-box binding protein associated factor 5 like

The product of this gene belongs to the WD-repeat TAF5 family of proteins. This gene encodes a protein that is a component of the PCAF histone acetylase complex. The PCAF histone acetylase complex, which is composed of more than 20 polypeptides some of which are TAFs, is required for myogenic transcription and differentiation. TAFs may participate in basal transcription, serve as coactivators, function in promoter recognition or modify general transcription factors to facilitate complex assembly and transcription initiation. The encoded protein is structurally similar to one of the histone-like TAFs, TAF5. Alternatively spliced transcript variants encoding different isoforms have been identified for this gene. [provided by RefSeq, Jul 2008].

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
ENST00000258281 O75529 328 230
ENST00000366675 O75529-2 131 109
ENST00000366674 Q5TDI7* 34 23

Gene Properties

Type
Protein Coding
Chromosome
1
Cytoband
1q42.13
Entrez ID
Aliases
PAF65B

Recurrent Mutations

All 230 amino-acid changes on canonical ENST00000258281 · 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 TAF5L · 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 TAF5L – 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
2/40 5%
0/0 0%
Endometrial Carcinoma
1/42 2%
17/612 3%
Thymic Epithelial Tumor
0/0 0%
1/39 3%
Non-Small Cell Lung Carcinoma
26/304 9%
14/1390 1%
Acute Myeloid Leukemia
2/90 2%
0/0 0%
Squamous Cell Lung Carcinoma
5/57 9%
9/810 1%
Gastric Carcinoma
2/74 3%
23/1809 1%
Bladder Carcinoma
3/58 5%
10/956 1%
Colorectal Carcinoma
15/143 10%
26/3239 1%
Melanoma
2/210 1%
21/1899 1%
Cervical Carcinoma
3/35 9%
2/422 0%
Neuroendocrine Tumour
8/154 5%
0/577 0%
Glioblastoma
1/98 1%
0/0 0%
Osteosarcoma
2/45 4%
0/166 0%
Gastrointestinal Stromal Tumour
0/0 0%
1/133 1%
Small Cell Lung Carcinoma
0/9 0%
5/752 1%
Other Solid Cancers
0/94 0%
9/1515 1%
Thyroid Gland Carcinoma
2/45 4%
7/1592 0%
Ovarian Carcinoma
1/109 1%
5/998 0%
Germ Cell Tumour
0/25 0%
1/169 1%
Head and Neck Carcinoma
1/85 1%
7/1574 0%
Glioma
1/52 2%
9/2127 0%
Mesothelioma
1/62 2%
0/165 0%
Medulloblastoma
0/0 0%
2/450 0%
Breast Carcinoma
0/144 0%
11/3264 0%
Hepatocellular Carcinoma
5/46 11%
2/2210 0%
Ewings Sarcoma
0/63 0%
1/262 0%
Biliary Tract Carcinoma
0/54 0%
3/950 0%
Pancreatic Carcinoma
1/89 1%
4/1611 0%
Prostate Carcinoma
2/13 15%
4/2105 0%

Mutation Distribution

Where TAF5L is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in TAF5L 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 493 mutations in TAF5L

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