ATAD3A

ATPase family AAA domain-containing protein 3A · Q9NVI7 · ATAD3A on Sugi Atlas →

0 patent compounds predicted against ATAD3A, 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 ATAD3A by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
PhII 5-Azacytidine Plus Valproic Acid and Eventually Atra in Intermediate II and High Risk MDS PHASE2COMPLETED
Trial of the Histone-Deacetylase Inhibitor ITF2357 Followed by Mechlorethamine in Relapsed/Refractory Hodgkin's Lymphoma PHASE1/PHASE2COMPLETED
Phenotypic and Genotypic Studies in Congenital and Early Onset Ataxias nanCOMPLETED
Genetic Basis of Abdominal Aortic Aneurysm nanCOMPLETED
Autophagy in Systemic Lupus Erythematosus nanUNKNOWN
A Patient-tailored Genetic/Biomarker/iPSC Combined Approach in ALS - PERMEALS nanRECRUITING
Molecular Studies on the Candidate Genes of Dopaminergic and Noradrenergic Systems in ADHD nanCOMPLETED
Core Stability Exercises and Hereditary Ataxia nanCOMPLETED
Autophagy Bladder Cancer nanUNKNOWN
PCD New Gene Discovery nanCOMPLETED
Pathogenetic Basis of Aortopathy and Aortic Valve Disease nanACTIVE_NOT_RECRUITING
Identification of Genes and Pathogenesis Involved in Familial Thoracic Aortic Aneurysm nanCOMPLETED
Familial Intracranial Aneurysm Study II nanCOMPLETED
Amyotrophic Lateral Sclerosis (ALS) Families Project nanRECRUITING
Classification, Functional Stratification and Biomarkers in Ciliopathy (CILLICORIRCM) nanCOMPLETED
Identification of New FTLD Genes nanUNKNOWN
Identifying Genes and Mutations Underlying Retinitis Pigmentosa and Allied Diseases nanUNKNOWN
Natural History Study of ATP1A3-related Disease nanUNKNOWN
Genotype-Phenotype Associations in Pediatric Cardiomyopathy (PCM GENES) nanCOMPLETED
Pathogenesis of Primary Ciliary Dyskinesia (PCD) Lung Disease nanRECRUITING
Delineating the Molecular Spectrum and the Clinical, Imaging and Neuronal Phenotype of Chopra-Amiel-Gordon Syndrome nanRECRUITING
Study on Genetically Affected Sporadic Thoracic Aortic Aneurysm and Dissection nanCOMPLETED
Mapping Novel Disease Genes for Dilated Cardiomyopathy nanCOMPLETED
Genetics of Endocrine Tumours - Familial Isolated Pituitary Adenoma - FIPA nanRECRUITING
New Genes Involved in Molecular Etiology of Rett Syndrome Through DNA Microarray Comparative Genomic Hybridization nanCOMPLETED
Collection of Blood Samples for DNA in Motor Neuron Disease nanCOMPLETED
Genetic Characterization of Parkinson's Disease nanCOMPLETED
Assessing the Polygenic Burden of Rare Disruptive Mutations in Parkinson's Disease nanUNKNOWN
Clinical and Genetic Analysis in Congenital Hypothyroidism Due to Thyroid Dysgenesis. nanCOMPLETED
Diagnosis of Primary Ciliary Dyskinesia nanCOMPLETED

Related proteins — ESM-2 sequence neighbours (a ATAD3A binder may also engage these)

ProteinNameSimilarity
A7YWC4 1.000 A7YWC4 →
Q3KRE0 1.000 Q3KRE0 →
Q925I1 1.000 Q925I1 →
Q9VEX6 1.000 Q9VEX6 →
Q58E76 1.000 Q58E76 →
Q6NVR9 1.000 Q6NVR9 →
Q20748 0.999 Q20748 →
Q6PAX2 0.998 Q6PAX2 →
ATAD3B ATPase family AAA domain-containing protein 3B 0.997 landscape →
Q5T2N8 0.994 Q5T2N8 →
Q9UQ90 0.988 Q9UQ90 →
P0A4V9 0.988 P0A4V9 →
A5U8T5 0.988 A5U8T5 →
A1R6Q4 0.987 A1R6Q4 →
B7KUB4 0.987 B7KUB4 →
P9WQN2 0.987 P9WQN2 →
A0PRE5 0.986 A0PRE5 →
A7H8E6 0.986 A7H8E6 →
A4FNI7 0.986 A4FNI7 →
Q73UL2 0.986 Q73UL2 →
A8M2A0 0.986 A8M2A0 →
B2B1M4 0.986 B2B1M4 →
Q0BXE2 0.986 Q0BXE2 →
A5CPU4 0.986 A5CPU4 →
Q2INY3 0.986 Q2INY3 →
P27472 0.986 P27472 →
B2GIP2 0.985 B2GIP2 →
P0A4G6 0.985 P0A4G6 →
Q7UDY6 0.985 Q7UDY6 →
A1WYM9 0.985 A1WYM9 →