ATP6V1A

V-type proton ATPase catalytic subunit A · P38606 · ATP6V1A on Sugi Atlas →

0 patent compounds predicted against ATP6V1A, 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 ATP6V1A by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
The Possible Efficacy and Safety of Lansoprazole Co-administration With Neoadjuvant Chemotherapy in Women With Breast Cancer PHASE3COMPLETED
Applying Proton Pump Inhibitor to Prevent and Treat Acute Fluctuating Hearing Loss in Patients With SLC26A4 Mutation PHASE2/PHASE3UNKNOWN
Copper Histidine Therapy for Menkes Diseases PHASE1/PHASE2COMPLETED
Efavirenz for Patients With Alzheimer's Disease PHASE1COMPLETED
Natural History Study of ATP1A3-related Disease nanUNKNOWN
Clinical and Genetic Analysis of Enlarged Vestibular Aqueducts nanCOMPLETED
Prescreening Study to Identify Potential Wilson Disease Participants for Gene-Editing Clinical Trial nanACTIVE_NOT_RECRUITING
Establishment of Human Cellular Disease Models for Wilson Disease nanCOMPLETED
Core Stability Exercises and Hereditary Ataxia nanCOMPLETED
Nuclear Myosin VI - a Therapeutic Target in Breast Cancer nanUNKNOWN
Diagnosis of Primary Ciliary Dyskinesia nanCOMPLETED
Study of Resting and Exercising Body Functioning in Freeman-Sheldon Syndrome and Related Conditions nanWITHDRAWN
Exome Analysis in Hearing Impaired Patients nanUNKNOWN
Phenotypic and Genotypic Studies in Congenital and Early Onset Ataxias nanCOMPLETED
Longitudinal Assessment of Atypical Tripeptidyl Peptidase 1 Enzyme Deficiency Patients nanACTIVE_NOT_RECRUITING
Role for Biochemical Assays and Kayser-Fleischer Rings in Diagnosis of Wilson Disease nanRECRUITING
Genetic Analysis of Patients With Pseudoxanthoma Elasticum nanCOMPLETED
Genetic Analysis of Hereditary Disorders of Hearing and Balance nanCOMPLETED
Validation of the RADIAL Algorithm for Diagnosis of Autosomal Recessive Cerebellar Ataxia nanRECRUITING
Genetics of Primary Ciliary Dyskinesia nanCOMPLETED
Natural History Study of SLC25A46 Mutation-related Mitochondriopathy nanCOMPLETED
Classification, Functional Stratification and Biomarkers in Ciliopathy (CILLICORIRCM) nanCOMPLETED
Genetic Testing in Detection of Late-Onset Hearing Loss nanCOMPLETED
Coproporphyrine Isomers and Methotrexate Elimination nanCOMPLETED
Genotype/Phenotype Correlation With Focus on Lung Function in Primary Ciliary Dyskinesia (PCD) nanUNKNOWN
Chronic Obstructive Pulmonary Disease Gene Localization nanCOMPLETED
Genetic Variations That Increase the Risk for Calcium Kidney Stones: a Family-based Study nanCOMPLETED
Study of Usher Syndromes, Type 1 and Type 2 nanCOMPLETED
Pediatric Cardiomyopathy Mutation Analysis nanRECRUITING
Exercise-mediated Rescue of Mitochondrial Dysfunctions Driving Insulin Resistance nanCOMPLETED

Related proteins — ESM-2 sequence neighbours (a ATP6V1A binder may also engage these)

ProteinNameSimilarity
P31404 1.000 P31404 →
P50516 1.000 P50516 →
Q76NM6 1.000 Q76NM6 →
Q29048 1.000 Q29048 →
Q5R5H2 1.000 Q5R5H2 →
Q27331 1.000 Q27331 →
Q90647 1.000 Q90647 →
O16109 1.000 O16109 →
Q5TTG1 1.000 Q5TTG1 →
P48602 1.000 P48602 →
O23654 1.000 O23654 →
Q2TJ56 1.000 Q2TJ56 →
Q61VZ4 1.000 Q61VZ4 →
P13548 1.000 P13548 →
Q9SM09 1.000 Q9SM09 →
Q9XW92 1.000 Q9XW92 →
Q8P2U6 1.000 Q8P2U6 →
P31406 1.000 P31406 →
P09469 1.000 P09469 →
Q9UVJ8 1.000 Q9UVJ8 →
P0DA07 1.000 P0DA07 →
Q1JNS8 1.000 Q1JNS8 →
Q5AJB1 1.000 Q5AJB1 →
Q5XE50 1.000 Q5XE50 →
Q6MAJ5 1.000 Q6MAJ5 →
P31405 1.000 P31405 →
Q1JDX0 1.000 Q1JDX0 →
Q8SQU9 1.000 Q8SQU9 →
P16140 1.000 P16140 →
Q38676 1.000 Q38676 →