LSG1

Large subunit GTPase 1 homolog · Q9H089 · LSG1 on Sugi Atlas →

0 patent compounds predicted against LSG1, 0 high-confidence (nearest known ligand ≥ 0.5)

Top predicted compounds (top 20 by supporting neighbours, then confidence)

CompoundConfidenceSupporting neighbours

Clinical trials — most relevant to LSG1 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Management of Retinitis Pigmentosa Via Combination of Wharton's Jelly-derived Mesenchymal Stem Cells and Magnovision PHASE3COMPLETED
R115777 to Treat Children With Neurofibromatosis Type 1 and Progressive Plexiform Neurofibromas PHASE2COMPLETED
Amyotrophic Lateral Sclerosis (ALS) Families Project nanRECRUITING
Autophagy in Systemic Lupus Erythematosus nanUNKNOWN
Study of the Pathophysiological Mechanisms Involved in Bleeding Events nanCOMPLETED
Evaluation of Serum Gasdermin D Level As a Potential Biomarker of Disease Activity in Vitiligo Patients nanUNKNOWN
Pilot Trial of Sirolimus/MEC in High Risk Acute Myelogenous Leukemia (AML) nanCOMPLETED
CML Pediatric ITK Response According to Molecular Identification at Diagnosis nanRECRUITING
Patient-derived Glioma Stem Cell Organoids nanACTIVE_NOT_RECRUITING
Investigating the Genetic Basis of Pseudoexfoliation Syndrome, Angle-closure Glaucoma and Primary Open-angle Glaucoma nanRECRUITING
Genetics and Psychopathology in the 22q11 Deletion Syndrome nanUNKNOWN
Transcriptomic Profile of Patients Treated With Different Modalities of Spinal Cord Stimulation nanUNKNOWN
Study of Skeletal Disorders and Short Stature nanCOMPLETED
Positional Cloning of the Gene(s) Responsible for Alagille Syndrome nanCOMPLETED
Molecular Genetics Study of Nasopharyngeal Carcinoma: Characterization of NCP Susceptibility Gene(s) nanCOMPLETED
Role of Polymorphisms in the IL-1 Gene Cluster nanCOMPLETED
Characterization of WAGR Syndrome and Other Chromosome 11 Gene Deletions nanCOMPLETED
Human Epilepsy Genetics--Neuronal Migration Disorders Study nanRECRUITING
Role of Sorcin and Annexin A3 in Breast Cancer Patients nanUNKNOWN
Mapping Disease Pathways for Biliary Atresia nanRECRUITING
Genetic Evaluation of NF1 and Scoliosis Patients nanCOMPLETED
Novel Biomarkers in the Neoplastic Progression of Barrett's Esophagus nanACTIVE_NOT_RECRUITING
Study of the Genetic and Epigenetic Causes of Recurrent Hydatidiform Moles nanACTIVE_NOT_RECRUITING
Long QT Syndrome-Population Genetics and Cardiac Studies nanCOMPLETED
Study of Tissue Samples in Predicting How Well Chemotherapy and Radiation Therapy Will Kill Cancer Cells in Patients With Squamous Cell Carcinoma of the Esophagus nanUNKNOWN
Developing Genetic Education for Smoking Cessation nanCOMPLETED
Studying Genes for Barrett's Esophagus in Brothers and Sisters nanUNKNOWN
Biomarkers of Lichen Sclerosus nanUNKNOWN
Assessing the Polygenic Burden of Rare Disruptive Mutations in Parkinson's Disease nanUNKNOWN
Diaphragmatic Hernia Research & Exploration, Advancing Molecular Science nanRECRUITING

Related proteins — ESM-2 sequence neighbours (a LSG1 binder may also engage these)

ProteinNameSimilarity
Q3UM18 1.000 Q3UM18 →
Q2YDM7 1.000 Q2YDM7 →
Q5BJT6 1.000 Q5BJT6 →
Q4R8L2 0.995 Q4R8L2 →
Q6NY89 0.992 Q6NY89 →
Q5ZJD3 0.991 Q5ZJD3 →
Q99LH1 0.989 Q99LH1 →
Q5R981 0.982 Q5R981 →
Q9V411 0.981 Q9V411 →
O14830 0.981 O14830 →
Q13823 0.981 Q13823 →
Q9W590 0.981 Q9W590 →
Q9CXF4 0.980 Q9CXF4 →
Q5RHD1 0.980 Q5RHD1 →
O35385 0.980 O35385 →
Q8BGE5 0.980 Q8BGE5 →
Q4KLT3 0.979 Q4KLT3 →
B3M1E1 0.979 B3M1E1 →
Q10LF7 0.979 Q10LF7 →
Q9SJF1 0.979 Q9SJF1 →
Q9SHS8 0.978 Q9SHS8 →
Q3T0J9 0.978 Q3T0J9 →
Q15326 0.978 Q15326 →
Q5ZLG3 0.978 Q5ZLG3 →
Q00578 0.978 Q00578 →
Q02395 0.978 Q02395 →
F1RA39 0.978 F1RA39 →
Q99P77 0.977 Q99P77 →
Q9BZF3 0.977 Q9BZF3 →
Q6NU40 0.977 Q6NU40 →