Sugi Predict

Sugi Predict / Targets / RABL6

RABL6

Rab-like protein 6 · Q3YEC7 · RABL6 on Sugi Atlas →

0 patent compounds predicted against RABL6, 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 RABL6 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
Study of the Pathophysiological Mechanisms Involved in Bleeding Events nanCOMPLETED
Assessing the Polygenic Burden of Rare Disruptive Mutations in Parkinson's Disease nanUNKNOWN
Identification of New Biomarkers of Insulin Resistance nanACTIVE_NOT_RECRUITING
Rab 32 Gene Polymorphisms as a Prognostic Factor in Leprosy Patients nanRECRUITING
Consortium On Risk for Early-onset Parkinson's Disease (CORE PD) nanCOMPLETED
Genetic Characterization of Parkinson's Disease nanCOMPLETED
Genetics of Rolandic Epilepsy nanCOMPLETED
Gene Analysis of Parkinson's Disease nanCOMPLETED
Autophagy in Systemic Lupus Erythematosus nanUNKNOWN
Genetic Study of Patients With Primary Ciliary Dyskinesia nanCOMPLETED
Rostock International Parkinson's Disease Study (ROPAD) nanCOMPLETED
Parkinson's Families Project nanRECRUITING
Natural History of Neuronal Ceroid Lipofuscinosis, Batten's CLN6 Diseae nanACTIVE_NOT_RECRUITING
Autophagy Bladder Cancer nanUNKNOWN
Whole-genome Sequencing Study in Patients With Diminished Ovarian Reserve nanUNKNOWN
Registry and Natural History of Epilepsy-Dyskinesia Syndromes nanRECRUITING
Genetic Basis of Non Syndromic Congenital Diaphragmatic Hernia nanCOMPLETED
Identifying Genes and Mutations Underlying Retinitis Pigmentosa and Allied Diseases nanUNKNOWN
Characterization of New Candidate Genes in Cases of Human Inherited Thrombocytopenia (CATCH) nanCOMPLETED
Study of Chediak-Higashi Syndrome nanRECRUITING
Clinical, Genetic, and Epidemiologic Study of Children and Adults With RASopathies nanRECRUITING
Biomarker Research in Inherited Movement Disorders nanRECRUITING
Whole Genome Scan of Extended Families With Familial Vocal Cord Paralysis nanCOMPLETED
Phenotypic and Genotypic Studies in Congenital and Early Onset Ataxias nanCOMPLETED
PCD New Gene Discovery nanCOMPLETED
New Genes Involved in Molecular Etiology of Rett Syndrome Through DNA Microarray Comparative Genomic Hybridization nanCOMPLETED

Related proteins — ESM-2 sequence neighbours (a RABL6 binder may also engage these)

ProteinNameSimilarity
Q08DA0 — 0.998 Q08DA0 →
Q5U3K5 — 0.994 Q5U3K5 →
Q96SB3 — 0.984 Q96SB3 →
Q6R891 — 0.984 Q6R891 →
O35274 — 0.984 O35274 →
Q9TUG2 — 0.983 Q9TUG2 →
O54935 — 0.982 O54935 →
Q60596 — 0.980 Q60596 →
P0DPB3 — 0.980 P0DPB3 →
Q3SX22 — 0.979 Q3SX22 →
A2A9T0 — 0.978 A2A9T0 →
Q9ET78 — 0.978 Q9ET78 →
Q91WD1 — 0.978 Q91WD1 →
Q9ET77 — 0.978 Q9ET77 →
Q8WVT3 — 0.978 Q8WVT3 →
Q9BWU0 — 0.977 Q9BWU0 →
P78524 — 0.977 P78524 →
Q9WTU0 — 0.977 Q9WTU0 →
A0JPQ7 — 0.977 A0JPQ7 →
Q1L8L6 — 0.977 Q1L8L6 →
Q8R5H6 — 0.977 Q8R5H6 →
Q60698 — 0.977 Q60698 →
Q5PQS6 — 0.977 Q5PQS6 →
Q62925 — 0.977 Q62925 →
Q80W04 — 0.977 Q80W04 →
Q9BR39 — 0.977 Q9BR39 →
Q07266 — 0.976 Q07266 →
Q53T59 — 0.976 Q53T59 →
Q9WU42 — 0.976 Q9WU42 →
Q9WVI9 — 0.976 Q9WVI9 →