GABRA2

Gamma-aminobutyric acid type A receptor subunit alpha2 P47869 GBRA2_HUMAN
Protein Coding Chr 4 4p12 Swiss-Prot reviewed Entrez 2555
Mutations
3,883
CL 443 · Tissue 3,415
Samples
599
CL 106 · Tissue 486
Peptides
474
unique mutant peptides
Transcripts
8
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
Mutations3,8834433,415
Samples599106486
Peptides47476416

Function

GABRA2 · Gamma-aminobutyric acid type A receptor subunit alpha2

GABA is the major inhibitory neurotransmitter in the mammalian brain where it acts at GABA-A receptors, which are ligand-gated chloride channels. Chloride conductance of these channels can be modulated by agents such as benzodiazepines that bind to the GABA-A receptor. At least 16 distinct subunits of GABA-A receptors have been identified. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2013].

Isoforms & Proteins

8 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
ENST00000381620 P47869 628 403
ENST00000507069 E9PBQ7* 582 402
ENST00000510861 P47869 564 389
ENST00000356504 P47869 561 386
ENST00000514090 P47869 561 386
ENST00000540012 A0A0A0MTM5* 497 345
ENST00000515082 G5E9Z6* 421 288
ENST00000507460 D6RAA9* 69 44

Gene Properties

Type
Protein Coding
Chromosome
4
Cytoband
4p12
Entrez ID
Aliases
DEE78EIEE78

Recurrent Mutations

All 403 amino-acid changes on canonical ENST00000381620 · 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 GABRA2 · 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 GABRA2 – 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
Squamous Cell Lung Carcinoma
9/57 16%
40/810 5%
Oral Cavity Carcinoma
3/54 6%
0/0 0%
Melanoma
14/210 7%
97/1899 5%
T-Lymphoblastic Leukemia
2/40 5%
0/0 0%
T-Cell Non-Hodgkins Lymphoma
1/26 4%
0/0 0%
Endometrial Carcinoma
3/42 7%
22/612 4%
Non-Small Cell Lung Carcinoma
17/304 6%
46/1390 3%
Other Solid Cancers
5/94 5%
42/1515 3%
Small Cell Lung Carcinoma
0/9 0%
20/752 3%
Colorectal Carcinoma
16/143 11%
54/3239 2%
Glioblastoma
2/98 2%
0/0 0%
Neuroendocrine Tumour
9/154 6%
3/577 1%
Bladder Carcinoma
3/58 5%
12/956 1%
Gastric Carcinoma
2/74 3%
24/1809 1%
Other Sarcomas
2/69 3%
6/699 1%
Germ Cell Tumour
0/25 0%
2/169 1%
Head and Neck Carcinoma
2/85 2%
15/1574 1%
Esophageal Carcinoma
0/23 0%
8/769 1%
Mesothelioma
1/62 2%
1/165 1%
Burkitts Lymphoma
2/32 6%
0/196 0%
Meningioma
0/3 0%
2/252 1%
Esophageal Squamous Cell Carcinoma
0/51 0%
19/2550 1%
Hepatocellular Carcinoma
2/46 4%
14/2210 1%
Cervical Carcinoma
0/35 0%
3/422 1%
Thyroid Gland Carcinoma
0/45 0%
8/1592 0%
Breast Carcinoma
5/144 3%
9/3264 0%
Glioma
1/52 2%
8/2127 0%
Biliary Tract Carcinoma
0/54 0%
4/950 0%
B-Cell Non-Hodgkins Lymphoma
2/88 2%
8/2534 0%
Ovarian Carcinoma
1/109 1%
3/998 0%

Mutation Distribution

Where GABRA2 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in GABRA2 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 53 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 3,883 mutations in GABRA2

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