DCUN1D3 — patent landscape

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

	Compound	Confidence	Supporting neighbours
	SCHEMBL8363012	0.40	1/20

Clinical trials — most relevant to DCUN1D3 by text similarity (a relevance ranking, not an exhaustive list)

Trial	Phase	Status
Mobilization and Collection of Peripheral Blood Stem Cells in Patients With Fanconi Anemia Using G-CSF and AMD3100	PHASE1/PHASE2	COMPLETED
Peptide Vaccine Focusing on Prevention of the Recurrence for Bladder Cancer	PHASE2	UNKNOWN
Human Leukocyte Antigen (HLA) - A*2402 Restricted Peptide Vaccine Therapy in Patients With Advanced Esophageal Cancer	PHASE1	COMPLETED
Human Leukocyte Antigen (HLA) - A*2402 Restricted Peptide Vaccine Therapy in Patients With Advanced Gastric Cancer	PHASE1	COMPLETED
Whole-genome Sequencing Study in Patients With Diminished Ovarian Reserve	nan	UNKNOWN
DICER1-related Pleuropulmonary Blastoma Cancer Predisposition Syndrome: A Natural History Study	nan	RECRUITING
PCD New Gene Discovery	nan	COMPLETED
New Signaling Pathway Targeting Systemic Lupus Erythematosus	nan	UNKNOWN
Prevalence of a Non-Expressing 11B Mutation in Aka Peoples of the Central African Republic	nan	COMPLETED
Genetic Studies of Strabismus, Congenital Cranial Dysinnervation Disorders (CCDDs), and Their Associated Anomalies	nan	RECRUITING
Diagnosis of Primary Ciliary Dyskinesia	nan	COMPLETED
Child Development and Genetic Biomarkers(II): Gene Verification and Data Integration	nan	UNKNOWN
MiRNA223 and HMGB1 as Apredictos for Drug Resistant Epilepsy	nan	UNKNOWN
Protein Expression as a Potential Diagnostic Biomarker of Cervical Dysplasia and/or Cancer	nan	COMPLETED
Genetics of Primary Ciliary Dyskinesia	nan	COMPLETED
Clinical and Genetic Analysis in Congenital Hypothyroidism Due to Thyroid Dysgenesis.	nan	COMPLETED
Genetic Analyses of Nonsyndromic and Syndromic Deafness in Pakistan	nan	ENROLLING_BY_INVITATION
Markers and Mechanisms of Macrovascular Disease in IDDM	nan	COMPLETED
Genetic Characterization of Parkinson's Disease	nan	COMPLETED
Association of SNPs in Long Intergenic Noncoding RNA 00511 (LINC00511) With Breast Cancer Among the Egyptian Population	nan	COMPLETED
Genetics of Endocrine Tumours - Familial Isolated Pituitary Adenoma - FIPA	nan	RECRUITING
Study of an Early Parenting Intervention for Children With Genetic Abnormalities and Mental Health Problems	nan	COMPLETED
Role of SF3B1 Mutation in Assessment of Acute and Chronic Lymphatic Leukemia	nan	NOT_YET_RECRUITING
Molecular Genetic Epidemiology of Endocardial Cushion Defects - SCOR in Pediatric Cardiovascular Disease	nan	COMPLETED
Speech and Short-term Memory Functions in Dyslexia: a Combined MEG and EEG Study	nan	UNKNOWN
Diagnosis of Prader-Willi Syndrome and Angelman Syndrome	nan	COMPLETED
Corpus Callosum Agenesis and Intellectual Disability	nan	COMPLETED
Genetic Analysis of Hereditary Disorders of Hearing and Balance	nan	COMPLETED
Muscle Tissue Bank for Muscular Dystrophy	nan	COMPLETED
Prognostic Value of Protein IMP3 Expression in Cervical Cancer	nan	COMPLETED

Related proteins — ESM-2 sequence neighbours (a DCUN1D3 binder may also engage these)

Protein	Name	Similarity
Q4V8B2	—	1.000	Q4V8B2 →
Q5R9G1	—	1.000	Q5R9G1 →
Q5E9V1	—	1.000	Q5E9V1 →
Q8K0V2	—	1.000	Q8K0V2 →
A4IHK8	—	0.991	A4IHK8 →
Q6DFA1	—	0.990	Q6DFA1 →
Q5RHX6	—	0.972	Q5RHX6 →
Q496Y0	—	0.971	Q496Y0 →
Q6ZT62	—	0.971	Q6ZT62 →
Q9UPU7	—	0.970	Q9UPU7 →
Q8K4S7	—	0.970	Q8K4S7 →
Q99MU3	—	0.968	Q99MU3 →
Q4R4I0	—	0.968	Q4R4I0 →
P97492	—	0.968	P97492 →
Q9CTY5	—	0.968	Q9CTY5 →
Q13474	—	0.968	Q13474 →
A4D2P6	—	0.968	A4D2P6 →
TERF2IP	Telomeric repeat-binding factor 2-interacting protein 1	0.968	landscape →
Q86XE3	—	0.968	Q86XE3 →
Q5T7W7	—	0.968	Q5T7W7 →
O54935	—	0.967	O54935 →
Q98TY6	—	0.967	Q98TY6 →
Q13905	—	0.967	Q13905 →
NOM1	Nucleolar MIF4G domain-containing protein 1	0.967	landscape →
Q9H6J7	—	0.967	Q9H6J7 →
Q9D2Q2	—	0.967	Q9D2Q2 →
Q9NVU0	—	0.967	Q9NVU0 →
INF2	Inverted formin-2	0.966	landscape →
Q0QWG9	—	0.966	Q0QWG9 →
Q9BZF2	—	0.966	Q9BZF2 →