TBPL1

TATA-box binding protein like 1 P62380 TBPL1_HUMAN
Protein Coding Chr 6 6q23.2 Swiss-Prot reviewed Entrez 9519
Mutations
200
CL 11 · Tissue 189
Samples
71
CL 6 · Tissue 65
Peptides
63
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
Mutations20011189
Samples71665
Peptides63558

Function

TBPL1 · TATA-box binding protein like 1

This gene encodes a member of the TATA box-binding protein family. TATA box-binding proteins play a critical role in transcription by RNA polymerase II as components of the transcription factor IID (TFIID) complex. The encoded protein does not bind to the TATA box and initiates transcription from TATA-less promoters. This gene plays a critical role in spermatogenesis, and single nucleotide polymorphisms in this gene may be associated with male infertility. Alternatively spliced transcript variants have been observed for this gene, and a pseudogene of this gene is located on the long arm of chromosome 3. [provided by RefSeq, Nov 2011].

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
ENST00000237264 P62380 72 60
ENST00000613034 P62380 69 58
ENST00000367871 Q7Z6U2* 59 50

Gene Properties

Type
Protein Coding
Chromosome
6
Cytoband
6q23.2
Entrez ID
Aliases
MGC:8389MGC:9620STUDTLFTLPTRF2

Recurrent Mutations

All 60 amino-acid changes on canonical ENST00000237264 · 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 TBPL1 · 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 TBPL1 – 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
1/42 2%
7/612 1%
Glioblastoma
1/98 1%
0/0 0%
Cervical Carcinoma
0/35 0%
3/422 1%
Colorectal Carcinoma
3/143 2%
10/3239 0%
Gastric Carcinoma
0/74 0%
7/1809 0%
Melanoma
0/210 0%
7/1899 0%
Bladder Carcinoma
0/58 0%
3/956 0%
Plasma Cell Myeloma
0/44 0%
1/305 0%
Squamous Cell Lung Carcinoma
0/57 0%
2/810 0%
Non-Small Cell Lung Carcinoma
0/304 0%
3/1390 0%
Head and Neck Carcinoma
0/85 0%
3/1574 0%
Hepatocellular Carcinoma
0/46 0%
4/2210 0%
Esophageal Carcinoma
0/23 0%
1/769 0%
Other Sarcomas
0/69 0%
1/699 0%
Other Solid Cancers
1/94 1%
1/1515 0%
Breast Carcinoma
0/144 0%
3/3264 0%
Glioma
0/52 0%
2/2127 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
2/2550 0%
B-Cell Non-Hodgkins Lymphoma
0/88 0%
2/2534 0%
Pancreatic Carcinoma
0/89 0%
1/1611 0%
Prostate Carcinoma
0/13 0%
1/2105 0%
Other Blood Cancers
0/61 0%
1/2725 0%

Mutation Distribution

Where TBPL1 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in TBPL1 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 200 mutations in TBPL1

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