WDR82 — patent landscape

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

	Compound	Confidence	Supporting neighbours

Clinical trials — most relevant to WDR82 by text similarity (a relevance ranking, not an exhaustive list)

Trial	Phase	Status
Can We Achieve 'high-quality' Weight Loss Through Supplementation and Exercise? the TRIM MUSCLE Study	PHASE3	COMPLETED
Whole-genome Sequencing Study in Patients With Diminished Ovarian Reserve	nan	UNKNOWN
Delineating the Molecular Spectrum and the Clinical, Imaging and Neuronal Phenotype of Chopra-Amiel-Gordon Syndrome	nan	RECRUITING
Whole Genome Scan of Extended Families With Familial Vocal Cord Paralysis	nan	COMPLETED
Identification of the Genetic Causes of Rare Diseases With Negative Exome Findings	nan	UNKNOWN
Molecular Diagnosis of Syndromic or Isolated Severe Intellectual Disability Using Whole Exome Sequencing : a Pilot Study	nan	COMPLETED
Characterization of WAGR Syndrome and Other Chromosome 11 Gene Deletions	nan	COMPLETED
Child Development and Genetic Biomarkers(II): Gene Verification and Data Integration	nan	UNKNOWN
Application of Linkage Analysis in the Identification of Novel Hereditary Factors in Familial Aneurysms	nan	ACTIVE_NOT_RECRUITING
Study of a Candidate Gene Involved in Goldenhar Syndrome.	nan	COMPLETED
Characterization of New Candidate Genes in Cases of Human Inherited Thrombocytopenia (CATCH)	nan	COMPLETED
Classification, Functional Stratification and Biomarkers in Ciliopathy (CILLICORIRCM)	nan	COMPLETED
Better Delineation of DDX3X Related Phenotype and Epigenetic Signature.	nan	UNKNOWN
MEHMO Natural History and Biomarkers	nan	RECRUITING
UW Undiagnosed Genetic Diseases Program	nan	RECRUITING
Assessing the Polygenic Burden of Rare Disruptive Mutations in Parkinson's Disease	nan	UNKNOWN
Aberrant Splicings Due to Microsatellite Instability in Colorectal Cancer : Physiopathological and Clinical Impact	nan	UNKNOWN
PCD New Gene Discovery	nan	COMPLETED
Natural History and Genetic Studies of Usher Syndrome	nan	COMPLETED
The LD Lync Study - Natural History Study of Lipodystrophy Syndromes	nan	RECRUITING
Genetic Study of Patients With Primary Ciliary Dyskinesia	nan	COMPLETED
Genetics of Endocrine Tumours - Familial Isolated Pituitary Adenoma - FIPA	nan	RECRUITING
Diaphragmatic Hernia Research & Exploration, Advancing Molecular Science	nan	RECRUITING
Finding Genes With NGS Techniques in Whom Mutations Cause Neurological Diseases	nan	UNKNOWN
Genetic Characterization of Parkinson's Disease	nan	COMPLETED
Williams Syndrome (WS) and Supravalvar Aortic Stenosis (SVAS) DNA and Tissue Bank	nan	COMPLETED
Genetics of Primary Ciliary Dyskinesia	nan	COMPLETED
Identification of Genes and Pathogenesis Involved in Familial Thoracic Aortic Aneurysm	nan	COMPLETED
Exome Sequencing Study in Cardiomyopathy to Identify New Risk Variants	nan	UNKNOWN
Target of Suv420h1/2 in Hepatocytes	nan	RECRUITING

Related proteins — ESM-2 sequence neighbours (a WDR82 binder may also engage these)

Protein	Name	Similarity
Q8BFQ4	—	1.000	Q8BFQ4 →
Q5ZMV7	—	1.000	Q5ZMV7 →
Q58E77	—	1.000	Q58E77 →
Q6GL39	—	1.000	Q6GL39 →
Q640J6	—	0.998	Q640J6 →
Q6NV31	—	0.994	Q6NV31 →
Q99LC2	—	0.961	Q99LC2 →
Q5R8K2	—	0.958	Q5R8K2 →
Q5BJQ6	—	0.958	Q5BJQ6 →
Q05048	—	0.956	Q05048 →
Q96EE3	—	0.945	Q96EE3 →
Q8R2U0	—	0.944	Q8R2U0 →
DCAF7	DDB1- and CUL4-associated factor 7	0.941	landscape →
A7YY75	—	0.940	A7YY75 →
Q5RAN6	—	0.939	Q5RAN6 →
Q8BHJ5	—	0.938	Q8BHJ5 →
P61963	—	0.936	P61963 →
Q9QXE7	—	0.935	Q9QXE7 →
Q6GPC6	—	0.935	Q6GPC6 →
TBL1XR1	F-box-like/WD repeat-containing protein TBL1XR1	0.934	landscape →
Q9V3J8	—	0.928	Q9V3J8 →
Q92747	—	0.928	Q92747 →
Q7SZM9	—	0.927	Q7SZM9 →
Q9BQ87	—	0.925	Q9BQ87 →
Q1JP79	—	0.925	Q1JP79 →
Q9R0Q6	—	0.923	Q9R0Q6 →
Q99PD4	—	0.922	Q99PD4 →
Q4FZW5	—	0.921	Q4FZW5 →
Q5M786	—	0.920	Q5M786 →
Q5U4Y8	—	0.920	Q5U4Y8 →