LAGE3

EKC/KEOPS complex subunit LAGE3 · Q14657 · LAGE3 on Sugi Atlas →

0 patent compounds predicted against LAGE3, 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 LAGE3 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
A Study of KRN23 in Pediatric Patients With X-linked Hypophosphatemic Rickets/Osteomalacia PHASE3COMPLETED
Cornelia De Lange Syndrome: Assessing Positive Effects of Lithium Treatment PHASE2/PHASE3RECRUITING
Optimizing IV Gentamicin in JEB PHASE1/PHASE2UNKNOWN
Perinatal Precision Medicine nanUNKNOWN
Identification of Genetic Basis of Atrioventricular Conduction Defects: From Congenital Forms to Degenerative Forms nanUNKNOWN
Efficacy of Visual and Perceptual Training on Visual Function for Operative Congenital Ectopia Lentis Children nanRECRUITING
MEHMO Natural History and Biomarkers nanRECRUITING
Decoding Developmental Disorders in Humams nanCOMPLETED
Genetic Variants in Linear Localized Scleroderma nanCOMPLETED
Neurovisual Function in CHARGE Syndrome nanUNKNOWN
Whole-genome Sequencing Study in Patients With Diminished Ovarian Reserve nanUNKNOWN
Investigating the Genetic Basis of Pseudoexfoliation Syndrome, Angle-closure Glaucoma and Primary Open-angle Glaucoma nanRECRUITING
NGS Panel of Incomplete Forms of Ocular Albinism nanCOMPLETED
New Strategies of Genetic Study of Patients With Oculocutaneous Albinism nanCOMPLETED
Whole Exome Sequencing in Coronary Artery Ectasia nanCOMPLETED
Idiopathic CD4 Lymphocytopenia nanCOMPLETED
Fast Exome for Diagnosis of Congenital Conditions in Infants Under 12 Months of Age Hospitalized in Intensive Care Unit nanCOMPLETED
Clinical Utility of Pediatric Whole Exome Sequencing nanCOMPLETED
Clinical Utility of Prenatal Whole Exome Sequencing nanCOMPLETED
Developing a Management Approach for Patients With Late-Onset Pompe Disease nanACTIVE_NOT_RECRUITING
Impact of Elastin Mediated Vascular Stiffness on End Organs nanCOMPLETED
Registry and Natural History of Epilepsy-Dyskinesia Syndromes nanRECRUITING
Classification, Functional Stratification and Biomarkers in Ciliopathy (CILLICORIRCM) nanCOMPLETED
Natural History Study of Patients With EYS-Associated RP nanRECRUITING
Whole Exome and Whole Genome Sequencing for Genotyping of Inherited and Congenital Eye Conditions nanRECRUITING
Study of a Candidate Gene Involved in Goldenhar Syndrome. nanCOMPLETED
Phenotype and Etiology of Pallister-Hall Syndrome nanCOMPLETED
Inbon Errors of Immunity Attending Assiut University Children&Amp;#39;s Hospital: a Single Center Study nanNOT_YET_RECRUITING
Genomic Study of Congenital Malformation nanUNKNOWN
Multidimensional Dynamic Early Warning System for Neonatal Necrotizing Enterocolitis: A Multicenter Clinical Study nanNOT_YET_RECRUITING

Related proteins — ESM-2 sequence neighbours (a LAGE3 binder may also engage these)

ProteinNameSimilarity
Q9CR70 0.949 Q9CR70 →
P78358 0.945 P78358 →
A0A0U1RRI6 0.939 A0A0U1RRI6 →
P0DPI3 0.935 P0DPI3 →
B7E321 0.933 B7E321 →
Q147X3 0.932 Q147X3 →
A0A0U1RR11 0.932 A0A0U1RR11 →
Q12962 0.932 Q12962 →
A6NNE9 0.931 A6NNE9 →
Q9CUB6 0.931 Q9CUB6 →
A6P320 0.930 A6P320 →
E9Q0B3 0.929 E9Q0B3 →
A1A5B6 0.928 A1A5B6 →
Q8K0H5 0.928 Q8K0H5 →
Q9BXQ6 0.928 Q9BXQ6 →
Q08DX6 0.928 Q08DX6 →
Q3TZ87 0.927 Q3TZ87 →
Q460M5 0.927 Q460M5 →
Q9WU40 0.927 Q9WU40 →
P55108 0.927 P55108 →
Q6DVA0 0.927 Q6DVA0 →
D3YXK1 0.926 D3YXK1 →
Q9Y6J9 0.926 Q9Y6J9 →
P83369 0.926 P83369 →
Q9JLG8 0.926 Q9JLG8 →
Q8CBH7 0.926 Q8CBH7 →
Q9P244 0.925 Q9P244 →
Q99MX7 0.925 Q99MX7 →
Q80TG9 0.925 Q80TG9 →
F5H4A9 0.925 F5H4A9 →