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DCUN1D5

DCN1-like protein 5 · Q9BTE7 · DCUN1D5 on Sugi Atlas →

1 patent compounds predicted against DCUN1D5, 1 high-confidence (nearest known ligand ≥ 0.5)

Top predicted compounds (top 20 by supporting neighbours, then confidence)

CompoundConfidenceSupporting neighbours
SCHEMBL8363012 SCHEMBL8363012 0.40 1/20

Clinical trials — most relevant to DCUN1D5 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Safety and Efficacy Study of Small Interfering RNA Molecule (Cand5) to Treat Diabetic Macular Edema PHASE2COMPLETED
Mobilization and Collection of Peripheral Blood Stem Cells in Patients With Fanconi Anemia Using G-CSF and AMD3100 PHASE1/PHASE2COMPLETED
Peptide Vaccine Focusing on Prevention of the Recurrence for Bladder Cancer PHASE2UNKNOWN
Human Leukocyte Antigen (HLA) - A*2402 Restricted Peptide Vaccine Therapy in Patients With Advanced Esophageal Cancer PHASE1COMPLETED
Human Leukocyte Antigen (HLA) - A*2402 Restricted Peptide Vaccine Therapy in Patients With Advanced Gastric Cancer PHASE1COMPLETED
Prevalence of a Non-Expressing 11B Mutation in Aka Peoples of the Central African Republic nanCOMPLETED
PCD New Gene Discovery nanCOMPLETED
DICER1-related Pleuropulmonary Blastoma Cancer Predisposition Syndrome: A Natural History Study nanRECRUITING
Whole-genome Sequencing Study in Patients With Diminished Ovarian Reserve nanUNKNOWN
Protein Expression as a Potential Diagnostic Biomarker of Cervical Dysplasia and/or Cancer nanCOMPLETED
Diagnosis of Primary Ciliary Dyskinesia nanCOMPLETED
New Signaling Pathway Targeting Systemic Lupus Erythematosus nanUNKNOWN
Child Development and Genetic Biomarkers(II): Gene Verification and Data Integration nanUNKNOWN
Genetics of Primary Ciliary Dyskinesia nanCOMPLETED
Genetic Studies of Strabismus, Congenital Cranial Dysinnervation Disorders (CCDDs), and Their Associated Anomalies nanRECRUITING
Biocollection in MyeloDysplastic Syndrome (P-MDS) nanRECRUITING
Role of SF3B1 Mutation in Assessment of Acute and Chronic Lymphatic Leukemia nanNOT_YET_RECRUITING
Autophagy in Systemic Lupus Erythematosus nanUNKNOWN
Chromosome 5Q Gene Variants and Asthma-Related Traits nanCOMPLETED
Hereditary Nonpolyposis Colorectal Cancer in Taiwan-Related Genetic Study and Clinical Applications nanUNKNOWN
The Value of circRNAs (hsa_circ_0004001) in Early Diagnosis of HCC nanUNKNOWN
Genetic Analysis of Hereditary Disorders of Hearing and Balance nanCOMPLETED
CML Pediatric ITK Response According to Molecular Identification at Diagnosis nanRECRUITING
Mapping Novel Disease Genes for Dilated Cardiomyopathy nanCOMPLETED
Genetic Characterization of Parkinson's Disease nanCOMPLETED
Immunogenetics of Visceral Leishmaniasis nanCOMPLETED
Genetic Analyses of Nonsyndromic and Syndromic Deafness in Pakistan nanENROLLING_BY_INVITATION
Pathogenesis of Primary Ciliary Dyskinesia (PCD) Lung Disease nanRECRUITING
MiRNA223 and HMGB1 as Apredictos for Drug Resistant Epilepsy nanUNKNOWN
Study of a Candidate Gene Involved in Goldenhar Syndrome. nanCOMPLETED

Related proteins — ESM-2 sequence neighbours (a DCUN1D5 binder may also engage these)

ProteinNameSimilarity
Q1RMX9 — 1.000 Q1RMX9 →
Q5RDF9 — 1.000 Q5RDF9 →
Q9CXV9 — 1.000 Q9CXV9 →
Q5PPL2 — 0.997 Q5PPL2 →
Q5RHX6 — 0.989 Q5RHX6 →
DCUN1D4 DCN1-like protein 4 0.980 landscape →
Q8CCA0 — 0.977 Q8CCA0 →
A4IG32 — 0.967 A4IG32 →
Q08331 — 0.966 Q08331 →
P47728 — 0.966 P47728 →
D2HZB0 — 0.963 D2HZB0 →
P07090 — 0.963 P07090 →
B1H2N3 — 0.962 B1H2N3 →
Q4V8B2 — 0.962 Q4V8B2 →
Q8K0V2 — 0.962 Q8K0V2 →
Q9BPX6 — 0.961 Q9BPX6 →
Q9QZ73 — 0.961 Q9QZ73 →
DCUN1D3 DCN1-like protein 3 0.960 landscape →
DCUN1D1 DCN1-like protein 1 0.960 landscape →
Q9BQI0 — 0.960 Q9BQI0 →
Q6P6Q9 — 0.959 Q6P6Q9 →
Q5E9V1 — 0.959 Q5E9V1 →
Q8VCX5 — 0.959 Q8VCX5 →
Q5VZK9 — 0.959 Q5VZK9 →
Q3ZBY3 — 0.959 Q3ZBY3 →
Q8HYN7 — 0.959 Q8HYN7 →
Q5ZKU1 — 0.958 Q5ZKU1 →
Q6PDL0 — 0.957 Q6PDL0 →
Q80UM3 — 0.957 Q80UM3 →
Q8BHL5 — 0.957 Q8BHL5 →