LTBP4

Latent transforming growth factor beta binding protein 4 Q8N2S1 LTBP4_HUMAN
Protein Coding Chr 19 19q13.2 Swiss-Prot reviewed Entrez 8425
Mutations
1,848
CL 234 · Tissue 1,591
Samples
643
CL 128 · Tissue 502
Peptides
531
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
Mutations1,8482341,591
Samples643128502
Peptides531102436

Function

LTBP4 · Latent transforming growth factor beta binding protein 4

The protein encoded by this gene binds transforming growth factor beta (TGFB) as it is secreted and targeted to the extracellular matrix. TGFB is biologically latent after secretion and insertion into the extracellular matrix, and sheds TGFB and other proteins upon activation. Defects in this gene may be a cause of cutis laxa and severe pulmonary, gastrointestinal, and urinary abnormalities. Three transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, May 2010].

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
ENST00000396819 Q8N2S1-2 659 482
ENST00000308370 Q8N2S1 598 460
ENST00000204005 A0A0C4DH07* 591 454

Gene Properties

Type
Protein Coding
Chromosome
19
Cytoband
19q13.2
Entrez ID
Aliases
ARCL1CLTBP-4LTBP4LLTBP4S

Recurrent Mutations

All 482 amino-acid changes on canonical ENST00000396819 · 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 LTBP4 · 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 LTBP4 – 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
6/40 15%
0/0 0%
Thymic Epithelial Tumor
0/0 0%
2/39 5%
Endometrial Carcinoma
6/42 14%
26/612 4%
Glioblastoma
4/98 4%
0/0 0%
Melanoma
12/210 6%
67/1899 4%
Cervical Carcinoma
1/35 3%
12/422 3%
Colorectal Carcinoma
10/143 7%
78/3239 2%
Acute Myeloid Leukemia
2/90 2%
0/0 0%
Gastric Carcinoma
4/74 5%
37/1809 2%
Bladder Carcinoma
3/58 5%
18/956 2%
Other Solid Cancers
0/94 0%
31/1515 2%
Thyroid Gland Carcinoma
2/45 4%
26/1592 2%
Non-Small Cell Lung Carcinoma
15/304 5%
11/1390 1%
Esophageal Carcinoma
1/23 4%
11/769 1%
Squamous Cell Lung Carcinoma
1/57 2%
12/810 1%
Hodgkins Lymphoma
1/16 6%
1/122 1%
Plasma Cell Myeloma
3/44 7%
2/305 1%
Biliary Tract Carcinoma
1/54 2%
13/950 1%
Burkitts Lymphoma
3/32 9%
0/196 0%
Hepatocellular Carcinoma
2/46 4%
26/2210 1%
Ovarian Carcinoma
7/109 6%
5/998 0%
Small Cell Lung Carcinoma
1/9 11%
6/752 1%
Other Sarcomas
0/69 0%
7/699 1%
Head and Neck Carcinoma
0/85 0%
14/1574 1%
Breast Carcinoma
8/144 6%
20/3264 1%
Pancreatic Carcinoma
6/89 7%
8/1611 0%
Neuroendocrine Tumour
5/154 3%
1/577 0%
Prostate Carcinoma
4/13 31%
13/2105 1%
Meningioma
0/3 0%
2/252 1%
Esophageal Squamous Cell Carcinoma
0/51 0%
19/2550 1%

Mutation Distribution

Where LTBP4 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in LTBP4 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 1,848 mutations in LTBP4

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