DNAJB11

DnaJ homolog subfamily B member 11 · Q9UBS4 · DNAJB11 on Sugi Atlas →

0 patent compounds predicted against DNAJB11, 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 DNAJB11 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Applying Proton Pump Inhibitor to Prevent and Treat Acute Fluctuating Hearing Loss in Patients With SLC26A4 Mutation PHASE2/PHASE3UNKNOWN
Mobilization and Collection of Peripheral Blood Stem Cells in Patients With Fanconi Anemia Using G-CSF and AMD3100 PHASE1/PHASE2COMPLETED
Study of Oral CNF2024 (BIIB021) in Advanced Solid Tumors PHASE1COMPLETED
Genetic Characterization of Parkinson's Disease nanCOMPLETED
Mapping Novel Disease Genes for Dilated Cardiomyopathy nanCOMPLETED
Studying Genes for Barrett's Esophagus in Brothers and Sisters nanUNKNOWN
Genetic Analysis of Hereditary Disorders of Hearing and Balance nanCOMPLETED
Shwachman Diamond Syndrome Registry and Study nanRECRUITING
Characterization of WAGR Syndrome and Other Chromosome 11 Gene Deletions nanCOMPLETED
PCD New Gene Discovery nanCOMPLETED
Identification of Genes and Pathogenesis Involved in Familial Thoracic Aortic Aneurysm nanCOMPLETED
Genetics of Primary Ciliary Dyskinesia nanCOMPLETED
Exome Analysis in Hearing Impaired Patients nanUNKNOWN
Signs and Symptoms of Genetic Abnormalities Linked to Inherited Heart Disease nanCOMPLETED
A Study Providing Genetic Testing to Find Those Who May Have Primary Ciliary Dyskinesia for Potential Clinical Trials nanACTIVE_NOT_RECRUITING
Natural History of Asphyxiating Thoracic Dystrophy (DTJ) nanCOMPLETED
Pathogenesis of Primary Ciliary Dyskinesia (PCD) Lung Disease nanRECRUITING
Early Onset and Familial Gastric Cancer Registry nanCOMPLETED
Registry and Natural History Study for Early Onset Hereditary Spastic Paraplegia nanRECRUITING
Identification of Genetic Causes of Calcific Aortic Valve Disease nanACTIVE_NOT_RECRUITING
Whole-genome Sequencing Study in Patients With Diminished Ovarian Reserve nanUNKNOWN
Molecular Diagnosis of Syndromic or Isolated Severe Intellectual Disability Using Whole Exome Sequencing : a Pilot Study nanCOMPLETED
Autophagy in Systemic Lupus Erythematosus nanUNKNOWN
Genetic Investigations in Spontaneous Coronary Artery Dissection (SCAD) nanRECRUITING
Genetic Determinants of Kawasaki Disease nanUNKNOWN
Family Risk Analysis of Substance Use in Attention Deficit Hyperactivity Disorder (ADHD) Youth Treated With Concerta nanCOMPLETED
Pathogenetic Basis of Aortopathy and Aortic Valve Disease nanACTIVE_NOT_RECRUITING
FASHION Fabry Disease Hypertrophic Cardiomyopathy and Infammation nanUNKNOWN
Genetic Analyses of Nonsyndromic and Syndromic Deafness in Pakistan nanENROLLING_BY_INVITATION
Genetic Studies of Tone Deafness nanCOMPLETED

Related proteins — ESM-2 sequence neighbours (a DNAJB11 binder may also engage these)

ProteinNameSimilarity
Q3ZBA6 1.000 Q3ZBA6 →
Q99KV1 1.000 Q99KV1 →
P81999 1.000 P81999 →
Q5RAJ6 1.000 Q5RAJ6 →
Q6TUG0 1.000 Q6TUG0 →
Q8MPX3 1.000 Q8MPX3 →
B9FHF3 1.000 B9FHF3 →
Q0JB88 0.999 Q0JB88 →
Q5R8J8 0.996 Q5R8J8 →
P43644 0.996 P43644 →
Q9VPQ2 0.996 Q9VPQ2 →
Q9LZK5 0.996 Q9LZK5 →
Q94AW8 0.996 Q94AW8 →
Q626I7 0.995 Q626I7 →
O35824 0.995 O35824 →
DNAJA2 DnaJ homolog subfamily A member 2 0.995 landscape →
Q2HJ94 0.995 Q2HJ94 →
Q04960 0.994 Q04960 →
P25491 0.994 P25491 →
Q3MI00 0.993 Q3MI00 →
Q9UDY4 0.993 Q9UDY4 →
Q9QYJ3 0.993 Q9QYJ3 →
Q9D832 0.992 Q9D832 →
Q2KIT4 0.992 Q2KIT4 →
Q9QYJ0 0.992 Q9QYJ0 →
P25303 0.992 P25303 →
Q9JMC3 0.992 Q9JMC3 →
P25685 0.991 P25685 →
P78004 0.990 P78004 →
Q03363 0.990 Q03363 →