GABRR2

Gamma-aminobutyric acid type A receptor subunit rho2 P28476 GBRR2_HUMAN
Protein Coding Chr 6 6q15 Swiss-Prot reviewed Entrez 2570
Mutations
271
CL 63 · Tissue 205
Samples
264
CL 63 · Tissue 198
Peptides
184
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
Mutations27163205
Samples26463198
Peptides18434152

Function

GABRR2 · Gamma-aminobutyric acid type A receptor subunit rho2

Gamma-aminobutyric acid (GABA) is the major inhibitory neurotransmitter in the mammalian brain where it acts at GABA receptors, which are ligand-gated chloride channels. The protein encoded by this gene is a member of the rho subunit family and is a component of the GABA type A receptor complex. This gene exists on chromosome 6q next to the gene encoding the rho 1 subunit of the GABA type A receptor, in a region thought to be associated with susceptibility for psychiatric disorders and epilepsy. Polymorphisms in this gene may also be associated with alcohol dependence, and general cognitive ability. [provided by RefSeq, Apr 2016].

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
ENST00000402938 P28476 271 184

Gene Properties

Type
Protein Coding
Chromosome
6
Cytoband
6q15
Entrez ID

Recurrent Mutations

All 184 amino-acid changes on canonical ENST00000402938 · 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 GABRR2 · 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 GABRR2 – 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
Chronic Myelogenous Leukemia
1/25 4%
0/0 0%
Endometrial Carcinoma
3/42 7%
14/612 2%
Acute Myeloid Leukemia
2/90 2%
0/0 0%
Gastrointestinal Stromal Tumour
0/0 0%
2/133 2%
Hodgkins Lymphoma
2/16 12%
0/122 0%
Colorectal Carcinoma
6/143 4%
41/3239 1%
Squamous Cell Lung Carcinoma
4/57 7%
7/810 1%
Germ Cell Tumour
2/25 8%
0/169 0%
Non-Small Cell Lung Carcinoma
1/304 0%
16/1390 1%
Gastric Carcinoma
1/74 1%
17/1809 1%
Melanoma
8/210 4%
10/1899 1%
Other Solid Cancers
2/94 2%
10/1515 1%
Head and Neck Carcinoma
2/85 2%
10/1574 1%
Biliary Tract Carcinoma
3/54 6%
4/950 0%
Bladder Carcinoma
2/58 3%
5/956 1%
Neuroendocrine Tumour
4/154 3%
1/577 0%
Small Cell Lung Carcinoma
0/9 0%
5/752 1%
Pancreatic Carcinoma
4/89 4%
6/1611 0%
Thyroid Gland Carcinoma
0/45 0%
8/1592 0%
Breast Carcinoma
3/144 2%
11/3264 0%
Glioma
0/52 0%
8/2127 0%
Ovarian Carcinoma
1/109 1%
3/998 0%
Ewings Sarcoma
1/63 2%
0/262 0%
Hepatocellular Carcinoma
0/46 0%
6/2210 0%
Other Sarcomas
0/69 0%
2/699 0%
Esophageal Carcinoma
0/23 0%
2/769 0%
Cervical Carcinoma
1/35 3%
0/422 0%
Non-Cancerous
0/104 0%
2/830 0%
Esophageal Squamous Cell Carcinoma
2/51 4%
3/2550 0%
Prostate Carcinoma
0/13 0%
4/2105 0%

Mutation Distribution

Where GABRR2 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in GABRR2 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 271 mutations in GABRR2

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