Sugi Predict

Sugi Predict / Targets / DNAJC9

DNAJC9

DnaJ homolog subfamily C member 9 · Q8WXX5 · DNAJC9 on Sugi Atlas →

0 patent compounds predicted against DNAJC9, 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 DNAJC9 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Study Evaluating the Safety and Tolerability of RCT1100 in Healthy and PCD Subjects PHASE1COMPLETED
FASHION Fabry Disease Hypertrophic Cardiomyopathy and Infammation nanUNKNOWN
Registry and Natural History Study for Early Onset Hereditary Spastic Paraplegia nanRECRUITING
Mapping Novel Disease Genes for Dilated Cardiomyopathy nanCOMPLETED
Acquirement of Clinical and Genomic Data to Diagnose in Rare Inherited Cardiomyopathy nanRECRUITING
Genetic Analysis of Familial Hypertrophic Cardiomyopathy nanCOMPLETED
Genetic Characterization of Parkinson's Disease nanCOMPLETED
Genetics of Pediatric-Onset Motor Neuron and Neuromuscular Diseases nanCOMPLETED
Autophagy in Systemic Lupus Erythematosus nanUNKNOWN
Exome Analysis in Hearing Impaired Patients nanUNKNOWN
Genetic Analysis of Hereditary Disorders of Hearing and Balance nanCOMPLETED
Idiopathic Dilated Cardiomyopathy nanCOMPLETED
PCD New Gene Discovery nanCOMPLETED
PCM1-JAK2 in Therapy Related Neoplasms nanUNKNOWN
Early Onset and Familial Gastric Cancer Registry nanCOMPLETED
Identification of Genes and Pathogenesis Involved in Familial Thoracic Aortic Aneurysm nanCOMPLETED
Genetics of Primary Ciliary Dyskinesia nanCOMPLETED
Chromosome 9 P Minus Syndrome nanRECRUITING
Exploration and Verification of DNA Methylolation in Early Screening of Esophageal Cancer nanUNKNOWN
Pathogenesis of Primary Ciliary Dyskinesia (PCD) Lung Disease nanRECRUITING
Hereditary Spastic Paraplegia Genomic Sequencing Initiative (HSPseq) nanRECRUITING
Genetics of Cardiovascular and Neuromuscular Disease nanRECRUITING
Biomarkers in SCOTland CardiomyopatHy Registry (Bio-SCOTCH) nanRECRUITING
Classification, Functional Stratification and Biomarkers in Ciliopathy (CILLICORIRCM) nanCOMPLETED
Signs and Symptoms of Genetic Abnormalities Linked to Inherited Heart Disease nanCOMPLETED
Diagnosis of Primary Ciliary Dyskinesia nanCOMPLETED
Genetic Analysis of Heart Channelopathies in Brazilian Patients and Their Relatives nanUNKNOWN
Study of a Candidate Gene Involved in Goldenhar Syndrome. nanCOMPLETED
Whole Genome Scan of Extended Families With Familial Vocal Cord Paralysis nanCOMPLETED
Genotype-Phenotype Associations in Pediatric Cardiomyopathy (PCM GENES) nanCOMPLETED

Related proteins — ESM-2 sequence neighbours (a DNAJC9 binder may also engage these)

ProteinNameSimilarity
Q91WN1 — 0.996 Q91WN1 →
Q9VGR7 — 0.982 Q9VGR7 →
Q6NWJ4 — 0.979 Q6NWJ4 →
Q5EAC6 — 0.978 Q5EAC6 →
Q8N1G2 — 0.978 Q8N1G2 →
Q5R981 — 0.977 Q5R981 →
P27008 — 0.977 P27008 →
Q8R3H9 — 0.976 Q8R3H9 →
Q9U6V6 — 0.976 Q9U6V6 →
Q9DBC3 — 0.976 Q9DBC3 →
C0HAV3 — 0.975 C0HAV3 →
Q66HA5 — 0.975 Q66HA5 →
Q6PGY6 — 0.974 Q6PGY6 →
B4KN00 — 0.974 B4KN00 →
CDC37 Hsp90 co-chaperone Cdc37 0.973 landscape →
Q6PFQ2 — 0.973 Q6PFQ2 →
Q7PGE8 — 0.973 Q7PGE8 →
Q9D8X2 — 0.973 Q9D8X2 →
Q7T0W1 — 0.973 Q7T0W1 →
Q5RAS1 — 0.973 Q5RAS1 →
Q8K339 — 0.973 Q8K339 →
P0C204 — 0.973 P0C204 →
Q7SXW2 — 0.972 Q7SXW2 →
Q61081 — 0.972 Q61081 →
Q5R5N9 — 0.972 Q5R5N9 →
CDC5L Cell division cycle 5-like protein 0.972 landscape →
A1XD97 — 0.972 A1XD97 →
Q9XHR2 — 0.972 Q9XHR2 →
A1A4I9 — 0.971 A1A4I9 →
F4IDS7 — 0.971 F4IDS7 →