Protein / target
Gamma-aminobutyric acid receptor subunit alpha-2
Protein at a glance
Biological role
GABA-gated chloride ion channel
Strongest disease association
Genetic developmental and epileptic encephalopathy
Therapeutic position
Established drug target
Derived from structured UniProt, Open Targets and literature data on this page.
Protein profile
Canonical identity and biological annotation from UniProt.
Function overview
Alpha subunit of the heteropentameric ligand-gated chloride channel gated by gamma-aminobutyric acid (GABA), a major inhibitory neurotransmitter in the brain.
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Alpha subunit of the heteropentameric ligand-gated chloride channel gated by gamma-aminobutyric acid (GABA), a major inhibitory neurotransmitter in the brain (PubMed:10449790, PubMed:29961870, PubMed:31032849). GABA-gated chloride channels, also named GABA(A) receptors (GABAAR), consist of five subunits arranged around a central pore and contain GABA active binding site(s) located at the alpha and beta subunit interfaces (By similarity). When activated by GABA, GABAARs selectively allow the flow of chloride anions across the cell membrane down their electrochemical gradient (PubMed:10449790). Chloride influx into the postsynaptic neuron following GABAAR opening decreases the neuron ability to generate a new action potential, thereby reducing nerve transmission (By similarity). The alpha-2 subunit exhibits synaptogenic activity together with beta-2 and very little to no activity together with beta-3, the gamma-2 subunit being necessary but not sufficient to induce rapid synaptic contacts formation (By similarity)
Subcellular location
Domains and Gene Ontology detail (20)Hide
Gene Ontology
- Caxon
- Cchloride channel complex
- Cdendrite membrane
- CGABA-A receptor complex
- CGABA-ergic synapse
- Cinhibitory synapse
- Cneuronal cell body
- Cplasma membrane
- Cpostsynapse
- Cpostsynaptic specialization membrane
- Csynaptic vesicle membrane
- Fbenzodiazepine receptor activity
Biological roles
What this protein does, drawn together from its UniProt function, Gene Ontology terms and Reactome pathways.
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Chloride transport
- ·Alpha subunit of the heteropentameric ligand-gated chloride channel gated by gamma-amino…
- ·chloride channel complex
- ·GABA-gated chloride ion channel activity
Ligand-gated signalling
- ·Alpha subunit of the heteropentameric ligand-gated chloride channel gated by gamma-amino…
- ·ligand-gated monoatomic ion channel activity involved in regulation of presynaptic membr…
- ·transmitter-gated monoatomic ion channel activity involved in regulation of postsynaptic…
Inhibitory neurotransmission
- ·GABA-ergic synapse
- ·inhibitory synapse
- ·inhibitory synapse assembly
- ·synaptic transmission, GABAergic
Ion channel gating
- ·GABA-gated chloride ion channel activity
- ·ligand-gated monoatomic ion channel activity involved in regulation of presynaptic membr…
- ·transmitter-gated monoatomic ion channel activity involved in regulation of postsynaptic…
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Concepts derived from UniProt GO Reactome — each badge above shows which sources supported that role.
Interaction neighbourhood
Proteins with the strongest functional or physical association. Node size and line weight reflect STRING confidence; hover or select a partner to inspect one association.
Functional and physical associations from STRING v12.0. Only associations with this protein are drawn — partner-to-partner links are not part of this evidence.
Approved medicines with mapped indications
Approved therapies targeting this protein, grouped by what they are approved to treat — the disease-first view of the medicines below. Relationships come from the canonical approved-indication graph (ChEMBL phase-4), the same source as the drug cards.
59 medicines meet Open Targets' target-level approved-medicine definition; the 9 shown here are those on this page with a canonical approved disease indication in the graph. Approved indications from ChEMBL (phase-4), via the canonical drug→disease graph.
Drugs targeting this protein
How approved and investigational drugs engage this protein — mechanism and action type, direct vs complex targeting, and how broadly each acts across other targets. A drug-first view (the section above groups the approved ones disease-first); direct binders with few recorded targets are listed first.
GABA-A receptor; anion channel positive allosteric modulator
Indicated for Epilepsy, Status Epilepticus
GABA-A receptor; anion channel positive allosteric modulator
GABA-A receptor; anion channel positive allosteric modulator
GABA-A receptor; anion channel positive allosteric modulator
GABA-A receptor; anion channel positive allosteric modulator
GABA-A receptor; anion channel positive allosteric modulator
Indicated for Seizures
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GABA-A receptor; anion channel positive allosteric modulator
Indicated for Epilepsy, Seizures
GABA-A receptor; anion channel positive allosteric modulator
Indicated for Anxiety Disorders, Status Epilepticus
GABA-A receptor; anion channel positive modulator
Indicated for Epilepsy, Migraine Disorders, Seizures
GABA-A receptor; anion channel positive allosteric modulator
Indicated for Epilepsy, Seizures
GABA-A receptor; anion channel positive allosteric modulator
Indicated for Epilepsy, Epileptic Syndromes, Seizures
GABA-A receptor; anion channel positive allosteric modulator
Indicated for Anxiety Disorders
ChEMBL mechanism, action type, target identity and approved indications. Open Targets clinical status.
Translational evidence
Why this target matters therapeutically, strongest evidence first. Disease associations are gene-level (via the gene that encodes this protein) and open into the full confidence synthesis; the development universe, tractability and safety annotations are target-level, from Open Targets.
Strongest disease associations · via encoding gene GABRA2
Gene-level evidence surfaced through the gene GABRA2that encodes this protein — not a direct protein–disease relationship. Ranked by Forefront's causal-directness weighting, so genetically- and clinically-evidenced diseases lead over ones that merely share the literature.
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The evidence agreement range shows how closely the independent evidence families agree — it is not a statistical confidence interval, and nothing here is fitted to outcome data. Derived from Open Targets evidence types under Forefront weighting; the per-type scores above show the calculation.
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Drug development
75 compounds recorded · 59 approved · 11 in clinical development · 5 earlier-stage
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Open Targets known-drugs universe. Drug name and highest clinical stage only — the disease relationship is NOT read from this slice (it carries trial-context noise); approved indications come from the canonical graph above.
Tractability
Small molecules — Strong
Antibodies — Emerging
Protein degraders — Emerging
View underlying tractability evidence (10)Hide
Raw Open Targets tractability assessment buckets, by modality.
Safety-related annotations
Terms indexed against this target in Open Targets' safety data, with their datasource. These are annotations, not causal claims: the direction of effect (whether activation or inhibition is implicated), species and evidence strength are not captured here, so an entry does not mean that modulating this target is known to cause that condition.
Clinical trials
Trials of drugs that target this protein — reached indirectly through those drugs, so a trial listed here studies the drug, not the protein. Ranked by active status, then clinical phase and recency, and spread across the targeting drugs.
View all trials (26)Hide
ClinicalTrials.gov via the drug-target graph.
What's happening now
Recent therapeutic activity around this target — regulatory actions, clinical trials and safety signals for 7 drugs that target this protein, plus publications where such a drug is a genuine subject. Every item is reached indirectly through the drug, not the protein itself; incidental mentions (a paper that merely measures a drug) and press items are excluded.
- Trial status changed
NMDAR Modulation As a Therapeutic Target and Probe of Neural Dysfunction in OCD
- Regulatory approval
Approval: TOPIRAMATE (ANDA220943)
- Trial status changed
A Phase 1, 3-part, Open-label Study to Evaluate the Effects of KarXT Administration on the Pharmacokinetics of Midazolam, Fexofenadine, and Digoxin in Healthy Adult Participants
- Trial status changed
A Phase 1 Study to Evaluate the Effect of Multiple Doses of ABBV-722 on the Pharmacokinetics of Cocktail Probe Substrates of CYP3A and Select Transporters in Healthy Adult Subjects
- Regulatory approval
Approval: PROPOFOL (ANDA220857)
- Regulatory approval
Approval: ALPRAZOLAM (ANDA213204)
- Trial status changed
Mechanistic Investigation of Therapies for Down Syndrome Regression Disorder
- Product recall
Recall (Class III): TOPIRAMATE
- Supplemental approval
Supplemental approval: PHENTERMINE AND TOPIRAMATE (NDA022580)
- New publicationNeonatal sevoflurane exposures inhibits DHHC5-mediated palmitoylation of TfR1 in oligodendrocytes, leading to hypomyelination and neurological impairments.
- Product recall
Recall (Class I): CLONAZEPAM
- Safety communication
Drug Safety Update: Topiramate (Topamax): introduction of new safety measures, including a Pregnancy Prevention Programme
Objective event titles are shown unmodified; the event kind and significance line are derived from structured fields. Forefront AttentionEvent stream aggregating Europe PMC Regulatory filings ClinicalTrials.gov.