ATP6V0C

V-type proton ATPase 16 kDa proteolipid subunit c · P27449 · ATP6V0C on Sugi Atlas →

0 patent compounds predicted against ATP6V0C, 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 ATP6V0C by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Copper Histidine Therapy for Menkes Diseases PHASE1/PHASE2COMPLETED
Genetic Analysis of Patients With Pseudoxanthoma Elasticum nanCOMPLETED
Natural History Study of ATP1A3-related Disease nanUNKNOWN
Study of Resting and Exercising Body Functioning in Freeman-Sheldon Syndrome and Related Conditions nanWITHDRAWN
Genetic Analysis of Hereditary Disorders of Hearing and Balance nanCOMPLETED
Biological Collection of Kidney Cells nanUNKNOWN
Role for Biochemical Assays and Kayser-Fleischer Rings in Diagnosis of Wilson Disease nanRECRUITING
Characteristics and Impacts of X-linked Hypohidrotic Ectodermal Dysplasia (XLHED) in Boys: An Observational International Study nanACTIVE_NOT_RECRUITING
Genetic and Biohumoral Factors Involved in Menière's Disease and Their Correlation With Phenotypes nanRECRUITING
Clinical and Genetic Analysis of Enlarged Vestibular Aqueducts nanCOMPLETED
Longitudinal Assessment of Atypical Tripeptidyl Peptidase 1 Enzyme Deficiency Patients nanACTIVE_NOT_RECRUITING
Prescreening Study to Identify Potential Wilson Disease Participants for Gene-Editing Clinical Trial nanACTIVE_NOT_RECRUITING
Diagnosis of Primary Ciliary Dyskinesia nanCOMPLETED
Natural History Study of SLC25A46 Mutation-related Mitochondriopathy nanCOMPLETED
Establishment of Human Cellular Disease Models for Wilson Disease nanCOMPLETED
Study of Usher Syndromes, Type 1 and Type 2 nanCOMPLETED
Classification, Functional Stratification and Biomarkers in Ciliopathy (CILLICORIRCM) nanCOMPLETED
Natural History Evaluation of Charcot Marie Tooth Disease (CMT) Types CMT1B, CMT2A, CMT4A, CMT4C, and Others nanRECRUITING
Phenotypic and Genotypic Studies in Congenital and Early Onset Ataxias nanCOMPLETED
Defining Treatment Outcomes and Genetic Architecture in Idiopathic Toe Walking* nanCOMPLETED
Genetic Testing in Detection of Late-Onset Hearing Loss nanCOMPLETED
New Strategies of Genetic Study of Patients With Oculocutaneous Albinism nanCOMPLETED
Disability Severity Scale (DSI) and Hereditary Motor and Sensory Neuropathy Overall Disability Scale (HMSN-R-ODS) nanCOMPLETED
CHOPXE - Analysis of Choriocapillaris Flow Deficits in Patients With Pseudoxanthoma Elasticum nanRECRUITING
Hereditary Spastic Paraplegia Genomic Sequencing Initiative (HSPseq) nanRECRUITING
Exome Analysis in Hearing Impaired Patients nanUNKNOWN
PCD New Gene Discovery nanCOMPLETED
Genetic Investigation of Cancer Predisposition nanNOT_YET_RECRUITING
GDF-15 as a Biomarker for Mitochondrial Disease nanCOMPLETED
Core Stability Exercises and Hereditary Ataxia nanCOMPLETED

Related proteins — ESM-2 sequence neighbours (a ATP6V0C binder may also engage these)

ProteinNameSimilarity
Q03105 1.000 Q03105 →
P23956 1.000 P23956 →
P63081 1.000 P63081 →
P63082 1.000 P63082 →
O18882 1.000 O18882 →
Q00607 0.998 Q00607 →
P23380 0.998 P23380 →
P25515 0.995 P25515 →
O16110 0.994 O16110 →
Q26250 0.993 Q26250 →
P31413 0.992 P31413 →
P55277 0.992 P55277 →
P31403 0.985 P31403 →
P50515 0.985 P50515 →
Q41773 0.957 Q41773 →
Q9Y874 0.948 Q9Y874 →
Q0IUB5 0.945 Q0IUB5 →
C0HLB4 0.944 C0HLB4 →
Q40585 0.944 Q40585 →
P59228 0.943 P59228 →
Q96473 0.943 Q96473 →
C0HLB5 0.943 C0HLB5 →
A2ZBW5 0.942 A2ZBW5 →
O24011 0.942 O24011 →
P68161 0.941 P68161 →
P23957 0.941 P23957 →
P0DH94 0.940 P0DH94 →
O22552 0.940 O22552 →
Q43434 0.940 Q43434 →
Q17046 0.940 Q17046 →