GTPBP4

GTP binding protein 4 Q9BZE4 GTPB4_HUMAN
Protein Coding Chr 10 10p15.3 Swiss-Prot reviewed Entrez 23560
Mutations
291
CL 49 · Tissue 241
Samples
276
CL 47 · Tissue 228
Peptides
211
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
Mutations29149241
Samples27647228
Peptides21133185

Function

GTPBP4 · GTP binding protein 4

GTP-binding proteins are GTPases and function as molecular switches that can flip between two states: active, when GTP is bound, and inactive, when GDP is bound. 'Active' in this context usually means that the molecule acts as a signal to trigger other events in the cell. When an extracellular ligand binds to a G-protein-linked receptor, the receptor changes its conformation and switches on the trimeric G proteins that associate with it by causing them to eject their GDP and replace it with GTP. The switch is turned off when the G protein hydrolyzes its own bound GTP, converting it back to GDP. But before that occurs, the active protein has an opportunity to diffuse away from the receptor and deliver its message for a prolonged period to its downstream target. [provided by RefSeq, Jul 2008].

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
ENST00000360803 Q9BZE4 291 211

Gene Properties

Type
Protein Coding
Chromosome
10
Cytoband
10p15.3
Entrez ID
Aliases
CRFGNGBNOG1

Recurrent Mutations

All 211 amino-acid changes on canonical ENST00000360803 · 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 GTPBP4 · 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 GTPBP4 – 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%
16/612 3%
Hodgkins Lymphoma
2/16 12%
1/122 1%
Mesothelioma
4/62 6%
0/165 0%
Melanoma
3/210 1%
28/1899 1%
Colorectal Carcinoma
9/143 6%
32/3239 1%
Non-Small Cell Lung Carcinoma
3/304 1%
17/1390 1%
Squamous Cell Lung Carcinoma
2/57 4%
8/810 1%
Small Cell Lung Carcinoma
0/9 0%
7/752 1%
Adrenocortical Carcinoma
0/3 0%
1/112 1%
Non-Cancerous
0/104 0%
7/830 1%
Neuroendocrine Tumour
4/154 3%
1/577 0%
Other Solid Cancers
2/94 2%
8/1515 1%
Bladder Carcinoma
2/58 3%
4/956 0%
Gastric Carcinoma
0/74 0%
11/1809 1%
Plasma Cell Myeloma
1/44 2%
1/305 0%
Ovarian Carcinoma
0/109 0%
6/998 1%
Germ Cell Tumour
0/25 0%
1/169 1%
Biliary Tract Carcinoma
0/54 0%
5/950 1%
Rhabdomyosarcoma
0/33 0%
1/171 1%
Head and Neck Carcinoma
0/85 0%
8/1574 1%
Osteosarcoma
1/45 2%
0/166 0%
Kidney Carcinoma
3/85 4%
6/1862 0%
Cervical Carcinoma
0/35 0%
2/422 0%
Burkitts Lymphoma
0/32 0%
1/196 1%
Meningioma
0/3 0%
1/252 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
10/2550 0%
Glioma
0/52 0%
8/2127 0%
Hepatocellular Carcinoma
0/46 0%
8/2210 0%
Ewings Sarcoma
0/63 0%
1/262 0%

Mutation Distribution

Where GTPBP4 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in GTPBP4 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 291 mutations in GTPBP4

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