Sugi Predict

Sugi Predict / Targets / WDR3

WDR3

WD repeat-containing protein 3 · Q9UNX4 · WDR3 on Sugi Atlas →

0 patent compounds predicted against WDR3, 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 WDR3 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Better Delineation of CDK13 Related Phenotype and Epigenetic Signature. nanUNKNOWN
Whole-genome Sequencing Study in Patients With Diminished Ovarian Reserve nanUNKNOWN
Better Delineation of DDX3X Related Phenotype and Epigenetic Signature. nanUNKNOWN
A Patient-tailored Genetic/Biomarker/iPSC Combined Approach in ALS - PERMEALS nanRECRUITING
Characterization of WAGR Syndrome and Other Chromosome 11 Gene Deletions nanCOMPLETED
Delineating the Molecular Spectrum and the Clinical, Imaging and Neuronal Phenotype of Chopra-Amiel-Gordon Syndrome nanRECRUITING
Molecular Diagnosis of Syndromic or Isolated Severe Intellectual Disability Using Whole Exome Sequencing : a Pilot Study nanCOMPLETED
Child Development and Genetic Biomarkers(II): Gene Verification and Data Integration nanUNKNOWN
Molecular and Clinical Studies of Primary Immunodeficiency Diseases nanUNKNOWN
Whole Genome Scan of Extended Families With Familial Vocal Cord Paralysis nanCOMPLETED
MEHMO Natural History and Biomarkers nanRECRUITING
Aberrant Splicings Due to Microsatellite Instability in Colorectal Cancer : Physiopathological and Clinical Impact nanUNKNOWN
Maternal Genes and Epimutations: Beckwith-Wiedemann Syndrome & Reproductive Risks nanRECRUITING
PCD New Gene Discovery nanCOMPLETED
iPSC Neurons From Adult Survivors of Childhood Cancer Who Have Persistent Vincristine-Induced Neuropathy nanCOMPLETED
Genetics of Endocrine Tumours - Familial Isolated Pituitary Adenoma - FIPA nanRECRUITING
Impact of Elastin Mediated Vascular Stiffness on End Organs nanCOMPLETED
Application of Linkage Analysis in the Identification of Novel Hereditary Factors in Familial Aneurysms nanACTIVE_NOT_RECRUITING
Characterization of New Candidate Genes in Cases of Human Inherited Thrombocytopenia (CATCH) nanCOMPLETED
Microarray Analysis in Syndromic Obesity nanCOMPLETED
Study to Investigate Genetic Causes of Severe Early Childhood Onset Obesity. nanRECRUITING
Study of a Candidate Gene Involved in Goldenhar Syndrome. nanCOMPLETED
Clinical and Genetic Analysis in Congenital Hypothyroidism Due to Thyroid Dysgenesis. nanCOMPLETED
Exome Sequencing Study in Cardiomyopathy to Identify New Risk Variants nanUNKNOWN
Studying Biomarkers in Samples From Younger Patients With Wilms Tumor nanCOMPLETED
Williams Syndrome (WS) and Supravalvar Aortic Stenosis (SVAS) DNA and Tissue Bank nanCOMPLETED
Genetic Study of Patients With Primary Ciliary Dyskinesia nanCOMPLETED
A Retrospective and Prospective Natural History Study of Patients With WHIM Syndrome nanWITHDRAWN
UW Undiagnosed Genetic Diseases Program nanRECRUITING
Diagnosis of Prader-Willi Syndrome and Angelman Syndrome nanCOMPLETED

Related proteins — ESM-2 sequence neighbours (a WDR3 binder may also engage these)

ProteinNameSimilarity
Q8BHB4 — 0.997 Q8BHB4 →
Q8BU03 — 0.991 Q8BU03 →
Q9C1X1 — 0.987 Q9C1X1 →
Q15269 — 0.986 Q15269 →
Q7ZXZ2 — 0.985 Q7ZXZ2 →
Q5RFQ3 — 0.984 Q5RFQ3 →
P87177 — 0.984 P87177 →
Q9LFE2 — 0.984 Q9LFE2 →
Q6S7B0 — 0.983 Q6S7B0 →
Q8TED0 — 0.983 Q8TED0 →
Q9C270 — 0.983 Q9C270 →
Q12220 — 0.982 Q12220 →
Q9USN3 — 0.982 Q9USN3 →
Q6AX60 — 0.982 Q6AX60 →
Q95JL5 — 0.982 Q95JL5 →
Q8VYZ5 — 0.981 Q8VYZ5 →
Q8C7V3 — 0.981 Q8C7V3 →
ELP1 Elongator complex protein 1 0.981 landscape →
P49846 — 0.981 P49846 →
Q6ED65 — 0.980 Q6ED65 →
F1SS88 — 0.980 F1SS88 →
Q9R099 — 0.980 Q9R099 →
Q4V7Y7 — 0.980 Q4V7Y7 →
Q5XGE2 — 0.980 Q5XGE2 →
Q04199 — 0.980 Q04199 →
Q16MY0 — 0.980 Q16MY0 →
O00423 — 0.980 O00423 →
Q7K4B3 — 0.979 Q7K4B3 →
A2RRU3 — 0.979 A2RRU3 →
Q91WQ5 — 0.979 Q91WQ5 →