Sugi Predict

Sugi Predict / Targets / WDR1

WDR1

WD repeat-containing protein 1 · O75083 · WDR1 on Sugi Atlas →

0 patent compounds predicted against WDR1, 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 WDR1 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Whole-genome Sequencing Study in Patients With Diminished Ovarian Reserve nanUNKNOWN
Characterization of WAGR Syndrome and Other Chromosome 11 Gene Deletions nanCOMPLETED
Long-read Genome Sequencing for the Molecular Diagnosis of Dystonia nanRECRUITING
Child Development and Genetic Biomarkers(II): Gene Verification and Data Integration nanUNKNOWN
Better Delineation of DDX3X Related Phenotype and Epigenetic Signature. nanUNKNOWN
Delineating the Molecular Spectrum and the Clinical, Imaging and Neuronal Phenotype of Chopra-Amiel-Gordon Syndrome nanRECRUITING
MEHMO Natural History and Biomarkers nanRECRUITING
Better Delineation of CDK13 Related Phenotype and Epigenetic Signature. nanUNKNOWN
Molecular Diagnosis of Syndromic or Isolated Severe Intellectual Disability Using Whole Exome Sequencing : a Pilot Study nanCOMPLETED
Study of a Candidate Gene Involved in Goldenhar Syndrome. nanCOMPLETED
Maternal Genes and Epimutations: Beckwith-Wiedemann Syndrome & Reproductive Risks nanRECRUITING
Whole Genome Scan of Extended Families With Familial Vocal Cord Paralysis nanCOMPLETED
Application of Linkage Analysis in the Identification of Novel Hereditary Factors in Familial Aneurysms nanACTIVE_NOT_RECRUITING
Aberrant Splicings Due to Microsatellite Instability in Colorectal Cancer : Physiopathological and Clinical Impact nanUNKNOWN
A Patient-tailored Genetic/Biomarker/iPSC Combined Approach in ALS - PERMEALS nanRECRUITING
Autophagy in Systemic Lupus Erythematosus nanUNKNOWN
A Retrospective and Prospective Natural History Study of Patients With WHIM Syndrome nanWITHDRAWN
PCD New Gene Discovery nanCOMPLETED
UW Undiagnosed Genetic Diseases Program nanRECRUITING
Genetic Characterization of Parkinson's Disease nanCOMPLETED
Mayo AVC Registry and Biobank nanRECRUITING
Exome Sequencing Study in Cardiomyopathy to Identify New Risk Variants nanUNKNOWN
Microarray Analysis in Syndromic Obesity nanCOMPLETED
Genetics of Endocrine Tumours - Familial Isolated Pituitary Adenoma - FIPA nanRECRUITING
Genetic Study of Patients With Primary Ciliary Dyskinesia nanCOMPLETED
Study of Gulf War Illness (GWI) by Comparing GWI and Healthy Veterans nanCOMPLETED
Neurodevelopmental Outcomes in Hypoplastic Left Heart Syndrome nanCOMPLETED
Study to Investigate Genetic Causes of Severe Early Childhood Onset Obesity. nanRECRUITING
NICUSeq: A Trial to Evaluate the Clinical Utility of Human Whole Genome Sequencing (WGS) Compared to Standard of Care in Acute Care Neonates and Infants nanCOMPLETED
Shwachman Diamond Syndrome Registry and Study nanRECRUITING

Related proteins — ESM-2 sequence neighbours (a WDR1 binder may also engage these)

ProteinNameSimilarity
Q2KJH4 — 1.000 Q2KJH4 →
O88342 — 1.000 O88342 →
Q9W7F2 — 1.000 Q9W7F2 →
Q5RKI0 — 1.000 Q5RKI0 →
O93277 — 1.000 O93277 →
Q6PAX7 — 1.000 Q6PAX7 →
Q9LV35 — 1.000 Q9LV35 →
Q6DIF4 — 0.999 Q6DIF4 →
Q9VU68 — 0.996 Q9VU68 →
Q9ZU34 — 0.994 Q9ZU34 →
A5DGL8 — 0.994 A5DGL8 →
Q11176 — 0.994 Q11176 →
O14301 — 0.994 O14301 →
P79083 — 0.992 P79083 →
Q95JL5 — 0.991 Q95JL5 →
Q26613 — 0.991 Q26613 →
A7TH19 — 0.990 A7TH19 →
Q6FL15 — 0.990 Q6FL15 →
A6ZMK5 — 0.990 A6ZMK5 →
P54686 — 0.990 P54686 →
P40217 — 0.989 P40217 →
Q759L2 — 0.989 Q759L2 →
E1BKF9 — 0.989 E1BKF9 →
P0CS32 — 0.989 P0CS32 →
O96622 — 0.988 O96622 →
P90587 — 0.988 P90587 →
Q6CI08 — 0.987 Q6CI08 →
F1SS88 — 0.987 F1SS88 →
P46680 — 0.987 P46680 →
Q9USN3 — 0.987 Q9USN3 →