ARHGDIB

Rho GDP dissociation inhibitor beta P52566 GDIR2_HUMAN
Protein Coding Chr 12 12p12.3 Swiss-Prot reviewed Entrez 397
Mutations
382
CL 82 · Tissue 297
Samples
136
CL 38 · Tissue 96
Peptides
100
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
Mutations38282297
Samples1363896
Peptides1002579

Function

ARHGDIB · Rho GDP dissociation inhibitor beta

Members of the Rho (or ARH) protein family (see MIM 165390) and other Ras-related small GTP-binding proteins (see MIM 179520) are involved in diverse cellular events, including cell signaling, proliferation, cytoskeletal organization, and secretion. The GTP-binding proteins are active only in the GTP-bound state. At least 3 classes of proteins tightly regulate cycling between the GTP-bound and GDP-bound states: GTPase-activating proteins (GAPs), guanine nucleotide-releasing factors (GRFs), and GDP-dissociation inhibitors (GDIs). The GDIs, including ARHGDIB, decrease the rate of GDP dissociation from Ras-like GTPases (summary by Scherle et al., 1993 [PubMed 8356058]).[supplied by OMIM, Dec 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
ENST00000228945 P52566 140 100
ENST00000541546 P52566 121 94
ENST00000541644 P52566 121 94

Gene Properties

Type
Protein Coding
Chromosome
12
Cytoband
12p12.3
Entrez ID
Aliases
D4GDIA2GDID4LYGDILy-GDIRAP1GN1

Recurrent Mutations

All 100 amino-acid changes on canonical ENST00000228945 · 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 ARHGDIB · 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 ARHGDIB – 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
Glioblastoma
5/98 5%
0/0 0%
T-Lymphoblastic Leukemia
2/40 5%
0/0 0%
Endometrial Carcinoma
1/42 2%
7/612 1%
Acute Myeloid Leukemia
1/90 1%
0/0 0%
Melanoma
3/210 1%
16/1899 1%
Squamous Cell Lung Carcinoma
3/57 5%
4/810 0%
Non-Small Cell Lung Carcinoma
6/304 2%
6/1390 0%
Plasma Cell Myeloma
2/44 5%
0/305 0%
Colorectal Carcinoma
5/143 4%
13/3239 0%
Germ Cell Tumour
0/25 0%
1/169 1%
Rhabdomyosarcoma
1/33 3%
0/171 0%
Medulloblastoma
0/0 0%
2/450 0%
Burkitts Lymphoma
0/32 0%
1/196 1%
Meningioma
0/3 0%
1/252 0%
Other Solid Cancers
0/94 0%
6/1515 0%
Bladder Carcinoma
2/58 3%
1/956 0%
Neuroendocrine Tumour
2/154 1%
0/577 0%
Thyroid Gland Carcinoma
0/45 0%
4/1592 0%
Esophageal Squamous Cell Carcinoma
2/51 4%
4/2550 0%
Hepatocellular Carcinoma
0/46 0%
5/2210 0%
Breast Carcinoma
0/144 0%
7/3264 0%
Glioma
0/52 0%
4/2127 0%
B-Lymphoblastic Leukemia
2/55 4%
2/2640 0%
Kidney Carcinoma
0/85 0%
3/1862 0%
Neuroblastoma
0/87 0%
2/1331 0%
Esophageal Carcinoma
0/23 0%
1/769 0%
Small Cell Lung Carcinoma
0/9 0%
1/752 0%
Other Sarcomas
0/69 0%
1/699 0%
Gastric Carcinoma
0/74 0%
2/1809 0%
Ovarian Carcinoma
0/109 0%
1/998 0%

Mutation Distribution

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

Mutation counts by tissue
Mutation Distribution

How many mutations in ARHGDIB 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 382 mutations in ARHGDIB

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