ARL1

ADP-ribosylation factor-like protein 1 · P40616 · ARL1 on Sugi Atlas →

0 patent compounds predicted against ARL1, 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 ARL1 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
Sirolimus Treatment in Patients With Autosomal Dominant Polycystic Kidney Disease: Renal Efficacy and Safety PHASE2COMPLETED
Scleral Buckling for Retinal Detachment Prevention in Genetically Confirmed Stickler Syndrome PHASE2WITHDRAWN
Effects of Vitamin B3 in Patients With Ataxia Telangiectasia PHASE2COMPLETED
Investigating the Effect of Vitamin A Supplementation on Retinitis Pigmentosa PHASE1COMPLETED
Study of the Pathophysiological Mechanisms Involved in Bleeding Events nanCOMPLETED
Autophagy in Systemic Lupus Erythematosus nanUNKNOWN
Genetic Characterization of Parkinson's Disease nanCOMPLETED
Identifying Genes and Mutations Underlying Retinitis Pigmentosa and Allied Diseases nanUNKNOWN
Classification, Functional Stratification and Biomarkers in Ciliopathy (CILLICORIRCM) nanCOMPLETED
The Cognitive Resilience Study nanCOMPLETED
Characterization of New Candidate Genes in Cases of Human Inherited Thrombocytopenia (CATCH) nanCOMPLETED
Genetics of Endocrine Tumours - Familial Isolated Pituitary Adenoma - FIPA nanRECRUITING
Molecular Genetic Epidemiology of Endocardial Cushion Defects - SCOR in Pediatric Cardiovascular Disease nanCOMPLETED
Studies on the Expression and Functions of RLIP76 in Blood Samples of Healthy Human Subjects nanWITHDRAWN
Dentatorubral-pallidoluysian Atrophy Natural History and Biomarkers Study nanUNKNOWN
Assessing the Polygenic Burden of Rare Disruptive Mutations in Parkinson's Disease nanUNKNOWN
GARM II: A Study on the Genetics of Age-related Maculopathy nanACTIVE_NOT_RECRUITING
The LD Lync Study - Natural History Study of Lipodystrophy Syndromes nanRECRUITING
Telomeres Length in Israeli Fibrotic ILD Patients nanENROLLING_BY_INVITATION
Characterization of WAGR Syndrome and Other Chromosome 11 Gene Deletions nanCOMPLETED
Biomarker for Homozygous Familial Hypercholesterolemia (BioHoFH) nanWITHDRAWN
Autophagy Bladder Cancer nanUNKNOWN
New Genes Involved in Molecular Etiology of Rett Syndrome Through DNA Microarray Comparative Genomic Hybridization nanCOMPLETED
Mapping Disease Pathways for Biliary Atresia nanRECRUITING
Clinical Characterization on PDE6A-related Retinitis Pigmentosa in Preparation to a Gene Therapy Trial nanCOMPLETED
Validation of the RADIAL Algorithm for Diagnosis of Autosomal Recessive Cerebellar Ataxia nanRECRUITING
Universal Rare Gene Study: A Registry and Natural History Study of Retinal Dystrophies Associated With Rare Disease-Causing Genetic Variants nanRECRUITING
Epidemiological and Genetic Studies of Body Mass Index nanCOMPLETED
Genetic Basis of Non Syndromic Congenital Diaphragmatic Hernia nanCOMPLETED

Related proteins — ESM-2 sequence neighbours (a ARL1 binder may also engage these)

ProteinNameSimilarity
Q2YDM1 1.000 Q2YDM1 →
P61212 1.000 P61212 →
P61211 1.000 P61211 →
P25160 1.000 P25160 →
Q96361 1.000 Q96361 →
Q75A26 1.000 Q75A26 →
P61750 1.000 P61750 →
Q5RCF1 1.000 Q5RCF1 →
P40940 1.000 P40940 →
P22274 1.000 P22274 →
ARF4 ADP-ribosylation factor 4 1.000 landscape →
P61204 0.999 P61204 →
Q25761 0.999 Q25761 →
Q5E9I6 0.999 Q5E9I6 →
O48649 0.999 O48649 →
P0CM16 0.999 P0CM16 →
Q06396 0.999 Q06396 →
O48920 0.999 O48920 →
P51822 0.998 P51822 →
P51644 0.998 P51644 →
P61206 0.998 P61206 →
Q10943 0.998 Q10943 →
ARF6 ADP-ribosylation factor 6 0.998 landscape →
Q7RVM2 0.998 Q7RVM2 →
P49702 0.998 P49702 →
P19146 0.998 P19146 →
P36579 0.998 P36579 →
P40946 0.997 P40946 →
P61207 0.997 P61207 →
Q9WUL7 0.997 Q9WUL7 →