DCUN1D4

DCN1-like protein 4 · Q92564 · DCUN1D4 on Sugi Atlas →

1 patent compounds predicted against DCUN1D4, 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 DCUN1D4 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Peptide Vaccine Focusing on Prevention of the Recurrence for Bladder Cancer PHASE2UNKNOWN
Mobilization and Collection of Peripheral Blood Stem Cells in Patients With Fanconi Anemia Using G-CSF and AMD3100 PHASE1/PHASE2COMPLETED
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
Novel Peptide Vaccination for Patients With Advanced Bladder Cancer PHASE1COMPLETED
DICER1-related Pleuropulmonary Blastoma Cancer Predisposition Syndrome: A Natural History Study nanRECRUITING
Whole-genome Sequencing Study in Patients With Diminished Ovarian Reserve nanUNKNOWN
Child Development and Genetic Biomarkers(II): Gene Verification and Data Integration nanUNKNOWN
Genetic Studies of Strabismus, Congenital Cranial Dysinnervation Disorders (CCDDs), and Their Associated Anomalies nanRECRUITING
Prevalence of a Non-Expressing 11B Mutation in Aka Peoples of the Central African Republic nanCOMPLETED
PCD New Gene Discovery nanCOMPLETED
Diagnosis of Primary Ciliary Dyskinesia nanCOMPLETED
New Signaling Pathway Targeting Systemic Lupus Erythematosus nanUNKNOWN
International PPB/DICER1 Registry nanRECRUITING
Genetics of Primary Ciliary Dyskinesia nanCOMPLETED
Association of SNPs in Long Intergenic Noncoding RNA 00511 (LINC00511) With Breast Cancer Among the Egyptian Population nanCOMPLETED
Urinary DENND1A.V2 as a Predictor of Pubertal Hyperandrogenemia nanSUSPENDED
Speech and Short-term Memory Functions in Dyslexia: a Combined MEG and EEG Study nanUNKNOWN
Genetic Analysis of Hereditary Disorders of Hearing and Balance nanCOMPLETED
Muscle Tissue Bank for Muscular Dystrophy nanCOMPLETED
Genetic Characterization of Parkinson's Disease nanCOMPLETED
Identification and Characterization of Novel Non-Coding Variants That Contribute to Genetic Disorders nanCOMPLETED
Markers and Mechanisms of Macrovascular Disease in IDDM nanCOMPLETED
Protein Expression as a Potential Diagnostic Biomarker of Cervical Dysplasia and/or Cancer nanCOMPLETED
Clinical and Genetic Analysis in Congenital Hypothyroidism Due to Thyroid Dysgenesis. nanCOMPLETED
Investigating Phenotypic, Epigenetic, and NeuroGenetic Traits in Rare and Ultra-rare Neurodevelopmental Disorders (Project PENGUIN) nanRECRUITING
Diamond Blackfan Anemia Registry (DBAR) nanRECRUITING
Genetics and Psychopathology in the 22q11 Deletion Syndrome nanUNKNOWN
The Influence of Genetic Variations in ELAPOR1 or ELAPOR2 on Insulin Secretion and Glucose Regulation in Humans nanUNKNOWN
Genetic Analyses of Nonsyndromic and Syndromic Deafness in Pakistan nanENROLLING_BY_INVITATION

Related proteins — ESM-2 sequence neighbours (a DCUN1D4 binder may also engage these)

ProteinNameSimilarity
Q8CCA0 1.000 Q8CCA0 →
Q5RHX6 0.998 Q5RHX6 →
DCUN1D5 DCN1-like protein 5 0.985 landscape →
Q1RMX9 0.978 Q1RMX9 →
Q5RDF9 0.974 Q5RDF9 →
Q9CXV9 0.971 Q9CXV9 →
Q5PPL2 0.970 Q5PPL2 →
Q9R1D7 0.968 Q9R1D7 →
PRKD1 Serine/threonine-protein kinase D1 0.964 landscape →
Q3LAC4 0.963 Q3LAC4 →
Q6DFZ1 0.962 Q6DFZ1 →
Q9BPX6 0.962 Q9BPX6 →
D2HZB0 0.961 D2HZB0 →
Q7YQL6 0.960 Q7YQL6 →
P84060 0.960 P84060 →
Q92538 0.960 Q92538 →
Q08BT5 0.960 Q08BT5 →
Q5U252 0.959 Q5U252 →
TLK2 Serine/threonine-protein kinase tousled-like 2 0.959 landscape →
O60890 0.959 O60890 →
USP47 Ubiquitin carboxyl-terminal hydrolase 47 0.959 landscape →
B1H2N3 0.959 B1H2N3 →
Q6P6Q9 0.959 Q6P6Q9 →
Q7YQL5 0.958 Q7YQL5 →
E1C1R4 0.958 E1C1R4 →
Q8VCX5 0.958 Q8VCX5 →
Q0IIL1 0.958 Q0IIL1 →
Q8BWW9 0.958 Q8BWW9 →
Q8BHL5 0.958 Q8BHL5 →
Q99MG9 0.958 Q99MG9 →