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Protein / target

Gamma-aminobutyric acid receptor subunit gamma-1

Encoded byGABRG1Q8N1C3Homo sapiensSwiss-Prot
Clinically validated
Therapeutic maturity
57
Approved medicines
Open Targets target-level
View by indication →
30
Clinical trials
Small-molecule tractable
Druggability
Approved Drug

Protein at a glance

Biological role

GABA-gated chloride ion channel

Strongest disease association

Epilepsy

Via encoding gene GABRG1 · Clinical evidence · score 0.61

Therapeutic position

Established drug target

Small molecules

Derived from structured UniProt, Open Targets and literature data on this page.

Protein profile

UniProt 2026_02

Canonical identity and biological annotation from UniProt.

Function overview

Gamma subunit of the heteropentameric ligand-gated chloride channel gated by gamma-aminobutyric acid (GABA), a major inhibitory neurotransmitter in the brain.

View complete UniProt function annotation

Gamma subunit of the heteropentameric ligand-gated chloride channel gated by gamma-aminobutyric acid (GABA), a major inhibitory neurotransmitter in the brain (PubMed:10449790). 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 interface(s) (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)

Subcellular location

Postsynaptic cell membraneCell membrane
Domains and Gene Ontology detail (13)

Gene Ontology

  • Cchloride channel complex
  • Cdendrite membrane
  • CGABA-A receptor complex
  • Cplasma membrane
  • Cpostsynapse
  • Cpostsynaptic membrane
  • FGABA receptor binding
  • FGABA-A receptor activity
  • FGABA-gated chloride ion channel activity
  • Pchloride transmembrane transport
  • Pgamma-aminobutyric acid signaling pathway
  • Pinhibitory synapse assembly

465 aa · 54 kDa

Biological roles

What this protein does, drawn together from its UniProt function, Gene Ontology terms and Reactome pathways.

Chloride transportUniProt · GOInhibitory neurotransmissionGOIon channel gatingGOLigand-gated signallingUniProt
View supporting evidence

Chloride transport

  • ·Gamma subunit of the heteropentameric ligand-gated chloride channel gated by gamma-amino…
  • ·chloride channel complex
  • ·GABA-gated chloride ion channel activity

Inhibitory neurotransmission

  • ·inhibitory synapse assembly
  • ·synaptic transmission, GABAergic

Ion channel gating

  • ·GABA-gated chloride ion channel activity

Ligand-gated signalling

  • ·Gamma subunit of the heteropentameric ligand-gated chloride channel gated by gamma-amino…

Concepts derived from UniProt GO Reactome — each badge above shows which sources supported that role.

Interaction neighbourhood

STRING v12.0

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.

PLCL1NSFTRAK2HAP1GABRB1GABRG2GABARAPGABRB2GABARA…GABRA1GABRG1

10 strongest partners — larger node and heavier line mean higher confidence

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

9 medicines · 6 areas

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.

Anxiety Disorders3 medicines
Status Epilepticus2 medicines
Epileptic Syndromes1 medicine
Migraine Disorders1 medicine

57 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

13

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.

Midazolam
ApprovedPositive allosteric modulator

GABA-A receptor; anion channel positive allosteric modulator

Indicated for Epilepsy, Status Epilepticus

Acts on a complex — shared with GABRG2, GABRB3, GABRG3 +12 more · 1 of 16 recorded protein targets — broad pharmacology

Isoflurane
ApprovedPositive allosteric modulator

GABA-A receptor; anion channel positive allosteric modulator

Acts on a complex — shared with GABRG2, GABRB3, GABRG3 +12 more · 1 of 23 recorded protein targets — broad pharmacology

Halothane
ApprovedPositive allosteric modulator

GABA-A receptor; anion channel positive allosteric modulator

Acts on a complex — shared with GABRG2, GABRB3, GABRG3 +12 more · 1 of 23 recorded protein targets — broad pharmacology

sevoflurane
ApprovedPositive allosteric modulator

GABA-A receptor; anion channel positive allosteric modulator

Acts on a complex — shared with GABRG2, GABRB3, GABRG3 +12 more · 1 of 23 recorded protein targets — broad pharmacology

propofol
ApprovedPositive allosteric modulator

GABA-A receptor; anion channel positive allosteric modulator

Acts on a complex — shared with GABRG2, GABRB3, GABRG3 +12 more · 1 of 16 recorded protein targets — broad pharmacology

clobazam
ApprovedPositive allosteric modulator

GABA-A receptor; anion channel positive allosteric modulator

Indicated for Seizures

Acts on a complex — shared with GABRG2, GABRB3, GABRG3 +12 more · 1 of 16 recorded protein targets — broad pharmacology

View all 13 targeting drugs
clonazepam
ApprovedPositive allosteric modulator

GABA-A receptor; anion channel positive allosteric modulator

Indicated for Epilepsy, Seizures

Acts on a complex — shared with GABRG2, GABRB3, GABRG3 +12 more · 1 of 16 recorded protein targets — broad pharmacology

lorazepam
ApprovedPositive allosteric modulator

GABA-A receptor; anion channel positive allosteric modulator

Indicated for Anxiety Disorders, Status Epilepticus

Acts on a complex — shared with GABRG2, GABRB3, GABRG3 +12 more · 1 of 16 recorded protein targets — broad pharmacology

meprobamate
ApprovedAgonist

GABA-A receptor; anion channel agonist

Indicated for Anxiety Disorders

Acts on a complex — shared with GABRG2, GABRB3, GABRG3 +12 more · 1 of 16 recorded protein targets — broad pharmacology

topiramate
ApprovedPositive modulator

GABA-A receptor; anion channel positive modulator

Indicated for Epilepsy, Migraine Disorders, Seizures

Acts on a complex — shared with GABRG2, GABRB3, GABRG3 +12 more · 1 of 37 recorded protein targets — broad pharmacology

cenobamate
ApprovedPositive allosteric modulator

GABA-A receptor; anion channel positive allosteric modulator

Indicated for Epilepsy, Seizures

Acts on a complex — shared with GABRG2, GABRB3, GABRG3 +12 more · 1 of 26 recorded protein targets — broad pharmacology

ganaxolone
ApprovedPositive allosteric modulator

GABA-A receptor; anion channel positive allosteric modulator

Indicated for Epilepsy, Epileptic Syndromes, Seizures

Acts on a complex — shared with GABRG2, GABRB3, GABRG3 +12 more · 1 of 16 recorded protein targets — broad pharmacology

alprazolam
ApprovedPositive allosteric modulator

GABA-A receptor; anion channel positive allosteric modulator

Indicated for Anxiety Disorders

Acts on a complex — shared with GABRG2, GABRB3, GABRG3 +12 more · 1 of 16 recorded protein targets — broad pharmacology

ChEMBL mechanism, action type, target identity and approved indications. Open Targets clinical status.

Translational evidence

Open Targets 26

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 GABRG1

Gene-level evidence surfaced through the gene GABRG1 that 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.

Epilepsy
0.75Moderately supported

Clinical evidence dominant · Open Targets 0.61

Migraine Disorders
0.75Moderately supported

Clinical evidence dominant · Open Targets 0.61

Major depressive disorder
0.75Moderately supported

Clinical evidence dominant · Open Targets 0.61

Alcoholism
0.73Moderately supported

Clinical evidence dominant · Open Targets 0.59

View evidence synthesis (4)
EpilepsyModerately supported
0.75
agreement 0.590.90
Clinical99%Literature1%

Open Targets aggregate 0.61 · 2 independent evidence families

Migraine DisordersModerately supported
0.75
agreement 0.590.90
Clinical100%Literature0%

Open Targets aggregate 0.61 · 2 independent evidence families

Major depressive disorderModerately supported
0.75
agreement 0.590.90
Clinical100%Literature1%

Open Targets aggregate 0.61 · 2 independent evidence families

AlcoholismModerately supported
0.73
agreement 0.580.89
Clinical98%Literature2%

Open Targets aggregate 0.59 · 2 independent evidence families

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.

Show all associations
Epilepsy0.61
Migraine Disorders0.61
Major depressive disorder0.61
Alcoholism0.59

Drug development

71 compounds recorded · 57 approved · 9 in clinical development · 5 earlier-stage

Open Targets' development universe — every compound recorded against the target at any stage, not all approved medicines. Distinct from the 13 drugs that target this protein in Forefront's canonical graph (9 with a mapped approved indication, shown above): these count different sets and are not a subset relation.

View all recorded compounds (10)
ALPRAZOLAMApproval
ISOFLURANEApproval
METHOHEXITALApproval
ENFLURANEApproval
TOPIRAMATEApproval
PAGOCLONEPhase 2 3
METHAQUALONE HYDROCHLORIDEUnknown
TETRAZEPAMUnknown
CLOTIAZEPAMApproval
MEPROBAMATEApproval

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 moleculesStrong

Approved Drug and High-Quality Ligand support this modality.

AntibodiesEmerging

Feasibility evidence (go cc high conf and uniprot loc med conf) — no clinical-stage drug of this modality recorded.

Protein degradersEmerging

Feasibility evidence (small molecule binder) — no clinical-stage drug of this modality recorded.

View underlying tractability evidence (8)
SM · Approved DrugSM · High-Quality LigandSM · Druggable FamilyAB · GO CC high confAB · UniProt loc med confAB · UniProt SigP or TMHMMAB · Human Protein Atlas locPR · Small Molecule Binder

Raw Open Targets tractability assessment buckets, by modality.

Safety-related annotations

decreased cardiac contractilityLynch et al. (2017)decreased memoryLynch et al. (2017)decreased convulsionsLynch et al. (2017)decreased locomotor activityLynch et al. (2017)increased sleepLynch et al. (2017)increased eatingLynch et al. (2017)increased respiratory rateLynch et al. (2017)decreased sleepLynch et al. (2017)muscle relaxationLynch et al. (2017)decreased body temperatureLynch et al. (2017)decreased painLynch et al. (2017)decreased blood pressureLynch et al. (2017)

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

30

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)

UNKNOWN · via topiramate · NCT06089356

ClinicalTrials.gov via the drug-target graph.

What's happening now

12

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.

  1. Regulatory approval2026-09-04

    Approval: TOPIRAMATE (ANDA219183)

    fda · regulatory · fda · via topiramate

  2. Product recall2026-08-31

    Recall (Class III): TOPIRAMATE

    fda · safety · fda · via topiramate

  3. Trial status changed2026-08-25

    The Effect of Low-Flow Sevoflurane and Low-Flow Desflurane Anesthesia on Postoperative Sore Throat in Laparoscopic Cholecystectomy Surgery

    Status changed to Completed · ClinicalTrials.gov · via sevoflurane

  4. Trial status changed2026-08-19

    A Phase 1, Open-Label, Two-Cohort Study to Assess the Effect of a Strong CYP3A4 Inducer on the Pharmacokinetics of Atumelnant and the Effect of Atumelnant on the Pharmacokinetics of CYP3A4, P-gp, and MATE1/2-K Substrates in Healthy Participants

    Status changed to Completed · ClinicalTrials.gov · via Midazolam

  5. Trial status changed2026-08-13

    NMDAR Modulation As a Therapeutic Target and Probe of Neural Dysfunction in OCD

    Status changed to Completed · ClinicalTrials.gov · via Midazolam

  6. Regulatory approval2026-07-22

    Approval: TOPIRAMATE (ANDA220943)

    fda · regulatory · fda · via topiramate

  7. Regulatory approval2026-07-14

    Approval: PROPOFOL (ANDA220857)

    fda · regulatory · fda · via propofol

  8. Regulatory approval2026-07-13

    Approval: ALPRAZOLAM (ANDA213204)

    fda · regulatory · fda · via alprazolam

  9. Trial status changed2026-07-13

    Mechanistic Investigation of Therapies for Down Syndrome Regression Disorder

    Status changed to Completed · ClinicalTrials.gov · via lorazepam

  10. Product recall2026-07-06

    Recall (Class III): TOPIRAMATE

    fda · safety · fda · via topiramate

  11. Product recall2024-11-18

    Recall (Class I): CLONAZEPAM

    fda · safety · fda · via clonazepam

  12. Safety communication2024-06-20

    Drug Safety Update: Topiramate (Topamax): introduction of new safety measures, including a Pregnancy Prevention Programme

    mhra · safety · mhra · via topiramate

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.