RABL3

Rab-like protein 3 · Q5HYI8 · RABL3 on Sugi Atlas →

0 patent compounds predicted against RABL3, 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 RABL3 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Safety and Efficacy of AAV9/AP4B1 (BFB-101) For Patients With AP4B1-related Hereditary Spastic Paraplegia Type 47 (SPG47) PHASE1/PHASE2NOT_YET_RECRUITING
Melpida: Recombinant Adeno-associated Virus (serotype 9) Encoding a Codon Optimized Human AP4M1 Transgene (hAP4M1opt) PHASE1/PHASE2RECRUITING
Effects of Lithium Therapy on Blood-based Therapeutic Targets in Parkinson's Disease. PHASE1COMPLETED
Nilotinib in Huntington's Disease PHASE1UNKNOWN
Rab 32 Gene Polymorphisms as a Prognostic Factor in Leprosy Patients nanRECRUITING
Study of the Pathophysiological Mechanisms Involved in Bleeding Events nanCOMPLETED
Identification of New Biomarkers of Insulin Resistance nanACTIVE_NOT_RECRUITING
Assessing the Polygenic Burden of Rare Disruptive Mutations in Parkinson's Disease nanUNKNOWN
Fox BioNet Project: LRRK2-002 nanCOMPLETED
Lipa Gene Mutation in PED-LIPIGEN (Pediatric FH Subjects) nanUNKNOWN
Genetic Characterization of Parkinson's Disease nanCOMPLETED
Gene Analysis of Parkinson's Disease nanCOMPLETED
Whole-genome Sequencing Study in Patients With Diminished Ovarian Reserve nanUNKNOWN
Rostock International Parkinson's Disease Study (ROPAD) nanCOMPLETED
Autophagy in Systemic Lupus Erythematosus nanUNKNOWN
LRRK2 Activity and Markers of Parkinson's Disease in G2385R Carriers nanCOMPLETED
Clinical, Genetic, and Epidemiologic Study of Children and Adults With RASopathies nanRECRUITING
Biomarker Research in Inherited Movement Disorders nanRECRUITING
Parkinson's Families Project nanRECRUITING
Study of Chediak-Higashi Syndrome nanRECRUITING
Consortium On Risk for Early-onset Parkinson's Disease (CORE PD) nanCOMPLETED
Genetic Study of Patients With Primary Ciliary Dyskinesia nanCOMPLETED
Study of the Genetic Factors Involved in Autism and Related Disorders nanRECRUITING
miRNAs Profiling in Parkinson's Disease nanCOMPLETED
Genetics of Rolandic Epilepsy nanCOMPLETED
Registry and Natural History of Epilepsy-Dyskinesia Syndromes nanRECRUITING
Pathogenesis of Primary Ciliary Dyskinesia (PCD) Lung Disease nanRECRUITING
Clinical Genetics Branch Eligibility Screening Survey nanNOT_YET_RECRUITING
AV133 Longitudinal Imaging Study in Patients With Early and Prdromal Parkinson's Disease nanRECRUITING
Identification of Genetic Basis of Atrioventricular Conduction Defects: From Congenital Forms to Degenerative Forms nanUNKNOWN

Related proteins — ESM-2 sequence neighbours (a RABL3 binder may also engage these)

ProteinNameSimilarity
Q6GPS4 1.000 Q6GPS4 →
Q5ZKR4 1.000 Q5ZKR4 →
A4IHM6 1.000 A4IHM6 →
Q32LJ6 0.999 Q32LJ6 →
Q6TNS7 0.997 Q6TNS7 →
Q9D4V7 0.996 Q9D4V7 →
Q5M8K8 0.964 Q5M8K8 →
Q66JN8 0.963 Q66JN8 →
Q5RFI2 0.962 Q5RFI2 →
Q9NX57 0.962 Q9NX57 →
Q9JKF8 0.962 Q9JKF8 →
Q7L523 0.961 Q7L523 →
Q80X95 0.961 Q80X95 →
O94844 0.961 O94844 →
Q9TS33 0.961 Q9TS33 →
Q05B56 0.961 Q05B56 →
O35626 0.961 O35626 →
Q9BYZ6 0.960 Q9BYZ6 →
Q99KL7 0.960 Q99KL7 →
A2AGL3 0.960 A2AGL3 →
Q9Y272 0.960 Q9Y272 →
Q63486 0.959 Q63486 →
P35295 0.959 P35295 →
Q6P4T2 0.959 Q6P4T2 →
Q3SWY9 0.959 Q3SWY9 →
Q7SXV1 0.959 Q7SXV1 →
P51157 0.958 P51157 →
Q676U5 0.958 Q676U5 →
Q9UKT5 0.958 Q9UKT5 →
Q15413 0.958 Q15413 →