GDI2

GDP dissociation inhibitor 2 P50395 GDIB_HUMAN
Protein Coding Chr 10 10p15.1 Swiss-Prot reviewed Entrez 2665
Mutations
295
CL 44 · Tissue 250
Samples
163
CL 33 · Tissue 129
Peptides
137
unique mutant peptides
Transcripts
2
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
Mutations29544250
Samples16333129
Peptides13721117

Function

GDI2 · GDP dissociation inhibitor 2

GDP dissociation inhibitors are proteins that regulate the GDP-GTP exchange reaction of members of the rab family, small GTP-binding proteins of the ras superfamily, that are involved in vesicular trafficking of molecules between cellular organelles. GDIs slow the rate of dissociation of GDP from rab proteins and release GDP from membrane-bound rabs. GDI2 is ubiquitously expressed. The GDI2 gene contains many repetitive elements indicating that it may be prone to inversion/deletion rearrangements. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2008].

Isoforms & Proteins

2 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
ENST00000380191 P50395 166 129
ENST00000380181 P50395-2 129 108

Gene Properties

Type
Protein Coding
Chromosome
10
Cytoband
10p15.1
Entrez ID
Aliases
HEL-S-46eRABGDIB

Recurrent Mutations

All 129 amino-acid changes on canonical ENST00000380191 · 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 GDI2 · 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 GDI2 – 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
3/42 7%
8/612 1%
Bladder Carcinoma
1/58 2%
8/956 1%
Hodgkins Lymphoma
0/16 0%
1/122 1%
Gastric Carcinoma
0/74 0%
13/1809 1%
Colorectal Carcinoma
3/143 2%
20/3239 1%
Neuroendocrine Tumour
4/154 3%
1/577 0%
Cervical Carcinoma
0/35 0%
3/422 1%
Melanoma
1/210 0%
10/1899 1%
Other Sarcomas
2/69 3%
2/699 0%
Hepatocellular Carcinoma
2/46 4%
9/2210 0%
Non-Small Cell Lung Carcinoma
2/304 1%
6/1390 0%
Squamous Cell Lung Carcinoma
0/57 0%
4/810 0%
Mesothelioma
1/62 2%
0/165 0%
Esophageal Carcinoma
0/23 0%
3/769 0%
Head and Neck Carcinoma
0/85 0%
6/1574 0%
Ovarian Carcinoma
4/109 4%
0/998 0%
Esophageal Squamous Cell Carcinoma
2/51 4%
7/2550 0%
Non-Cancerous
1/104 1%
2/830 0%
Other Solid Cancers
1/94 1%
4/1515 0%
Plasma Cell Myeloma
0/44 0%
1/305 0%
Medulloblastoma
0/0 0%
1/450 0%
Neuroblastoma
3/87 3%
0/1331 0%
Pancreatic Carcinoma
0/89 0%
3/1611 0%
Breast Carcinoma
0/144 0%
6/3264 0%
B-Cell Non-Hodgkins Lymphoma
0/88 0%
4/2534 0%
Glioma
0/52 0%
3/2127 0%
Small Cell Lung Carcinoma
0/9 0%
1/752 0%
Biliary Tract Carcinoma
0/54 0%
1/950 0%
Other Blood Cancers
1/61 2%
1/2725 0%

Mutation Distribution

Where GDI2 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in GDI2 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 295 mutations in GDI2

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