Sugi Predict

Sugi Predict / Targets / DNAJB12

DNAJB12

DnaJ homolog subfamily B member 12 · Q9NXW2 · DNAJB12 on Sugi Atlas →

0 patent compounds predicted against DNAJB12, 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 DNAJB12 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 Analysis of Hereditary Disorders of Hearing and Balance nanCOMPLETED
Mapping Novel Disease Genes for Dilated Cardiomyopathy nanCOMPLETED
Studying Genes for Barrett's Esophagus in Brothers and Sisters nanUNKNOWN
Genetics of Primary Ciliary Dyskinesia nanCOMPLETED
Identification of Genes and Pathogenesis Involved in Familial Thoracic Aortic Aneurysm nanCOMPLETED
Pathogenesis of Primary Ciliary Dyskinesia (PCD) Lung Disease nanRECRUITING
PCD New Gene Discovery nanCOMPLETED
Signs and Symptoms of Genetic Abnormalities Linked to Inherited Heart Disease nanCOMPLETED
Genetic Characterization of Parkinson's Disease nanCOMPLETED
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
Shwachman Diamond Syndrome Registry and Study nanRECRUITING
A Study Providing Genetic Testing to Find Those Who May Have Primary Ciliary Dyskinesia for Potential Clinical Trials nanACTIVE_NOT_RECRUITING
Study of a Candidate Gene Involved in Goldenhar Syndrome. nanCOMPLETED
Registry and Natural History Study for Early Onset Hereditary Spastic Paraplegia nanRECRUITING
Muscle Tissue Bank for Muscular Dystrophy nanCOMPLETED
Limb Girdle Muscular Dystrophy Type 2E Recruitment Study nanUNKNOWN
Genetics and Psychopathology in the 22q11 Deletion Syndrome nanUNKNOWN
Genetic Analyses of Nonsyndromic and Syndromic Deafness in Pakistan nanENROLLING_BY_INVITATION
FASHION Fabry Disease Hypertrophic Cardiomyopathy and Infammation nanUNKNOWN
Genetic Analysis of Heart Channelopathies in Brazilian Patients and Their Relatives nanUNKNOWN
Genetic Analysis of Familial Hypertrophic Cardiomyopathy nanCOMPLETED
Immunogenetics of Visceral Leishmaniasis nanCOMPLETED
Pathogenetic Basis of Aortopathy and Aortic Valve Disease nanACTIVE_NOT_RECRUITING
Whole Exome and Whole Genome Sequencing for Genotyping of Inherited and Congenital Eye Conditions nanRECRUITING
The Congenital Dyserythropoietic Anemia Registry (CDAR) nanRECRUITING
Characterization of WAGR Syndrome and Other Chromosome 11 Gene Deletions nanCOMPLETED

Related proteins — ESM-2 sequence neighbours (a DNAJB12 binder may also engage these)

ProteinNameSimilarity
Q58DR2 — 1.000 Q58DR2 →
Q9QYI4 — 1.000 Q9QYI4 →
Q17438 — 1.000 Q17438 →
Q149L6 — 0.999 Q149L6 →
Q7ZXQ8 — 0.998 Q7ZXQ8 →
O13633 — 0.995 O13633 →
Q5R6H3 — 0.995 Q5R6H3 →
Q28I38 — 0.995 Q28I38 →
Q8GUN6 — 0.993 Q8GUN6 →
Q9CZJ9 — 0.993 Q9CZJ9 →
Q17433 — 0.991 Q17433 →
Q64332 — 0.991 Q64332 →
Q0IIE8 — 0.990 Q0IIE8 →
Q5EA26 — 0.990 Q5EA26 →
B6HU36 — 0.989 B6HU36 →
Q8TBM8 — 0.989 Q8TBM8 →
A0A0D1E2P6 — 0.989 A0A0D1E2P6 →
Q9QYI5 — 0.989 Q9QYI5 →
C7YIH6 — 0.989 C7YIH6 →
A5D989 — 0.988 A5D989 →
Q75E62 — 0.988 Q75E62 →
Q9NRR4 — 0.988 Q9NRR4 →
Q0WTI8 — 0.988 Q0WTI8 →
C9SNH6 — 0.988 C9SNH6 →
Q4WHN8 — 0.987 Q4WHN8 →
A8BM50 — 0.987 A8BM50 →
A6RJA2 — 0.987 A6RJA2 →
P35197 — 0.987 P35197 →
F4IF36 — 0.987 F4IF36 →
P92792 — 0.987 P92792 →