WDR26

WD repeat-containing protein 26 · Q9H7D7 · WDR26 on Sugi Atlas →

0 patent compounds predicted against WDR26, 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 WDR26 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Safety, Tolerability and Efficacy for CGF166 in Patients With Unilateral or Bilateral Severe-to-profound Hearing Loss PHASE1/PHASE2COMPLETED
Characterization of WAGR Syndrome and Other Chromosome 11 Gene Deletions nanCOMPLETED
WS-SAVE Study (Williams Syndrome Skin and Vessel Elasticity Study) nanCOMPLETED
Whole-genome Sequencing Study in Patients With Diminished Ovarian Reserve nanUNKNOWN
Application of Linkage Analysis in the Identification of Novel Hereditary Factors in Familial Aneurysms nanACTIVE_NOT_RECRUITING
Delineating the Molecular Spectrum and the Clinical, Imaging and Neuronal Phenotype of Chopra-Amiel-Gordon Syndrome nanRECRUITING
MEHMO Natural History and Biomarkers nanRECRUITING
A Retrospective and Prospective Natural History Study of Patients With WHIM Syndrome nanWITHDRAWN
Better Delineation of DDX3X Related Phenotype and Epigenetic Signature. nanUNKNOWN
Better Delineation of CDK13 Related Phenotype and Epigenetic Signature. nanUNKNOWN
UW Undiagnosed Genetic Diseases Program nanRECRUITING
Classification, Functional Stratification and Biomarkers in Ciliopathy (CILLICORIRCM) nanCOMPLETED
Molecular Diagnosis of Syndromic or Isolated Severe Intellectual Disability Using Whole Exome Sequencing : a Pilot Study nanCOMPLETED
PCD New Gene Discovery nanCOMPLETED
Child Development and Genetic Biomarkers(II): Gene Verification and Data Integration nanUNKNOWN
Impact of Elastin Mediated Vascular Stiffness on End Organs nanCOMPLETED
Characterization of New Candidate Genes in Cases of Human Inherited Thrombocytopenia (CATCH) nanCOMPLETED
A to Z Study Follow-up: Collection of DNA Data From Buccal Swabs nanUNKNOWN
A Genetic Family Cohort Study of Bipolar Disorder in Chinese Han Population nanUNKNOWN
Microarray Analysis in Syndromic Obesity nanCOMPLETED
Genetic Analysis of Fraser Syndrome and Fryns Syndrome nanCOMPLETED
Study of a Candidate Gene Involved in Goldenhar Syndrome. nanCOMPLETED
The Phenotyping and Genotyping of Taiwanese Patients With Obstructive Sleep Apnea nanUNKNOWN
Natural History and Genetic Studies of Usher Syndrome nanCOMPLETED
I-Tracking Neurodegeneration in Early Wolfram Syndrome nanCOMPLETED
Characterization of Angelman Syndrome nanCOMPLETED
Study to Investigate Genetic Causes of Severe Early Childhood Onset Obesity. nanRECRUITING
Markers and Mechanisms of Macrovascular Disease in IDDM nanCOMPLETED
Genetic Study of Patients With Primary Ciliary Dyskinesia nanCOMPLETED
Genetic, Dietary and Environmental Influences on Vitamin D Metabolism nanCOMPLETED

Related proteins — ESM-2 sequence neighbours (a WDR26 binder may also engage these)

ProteinNameSimilarity
Q8C6G8 1.000 Q8C6G8 →
Q28D01 0.996 Q28D01 →
Q5SP67 0.981 Q5SP67 →
F1LTR1 0.974 F1LTR1 →
Q9UKB1 0.962 Q9UKB1 →
A0A2R8RWN9 0.960 A0A2R8RWN9 →
Q32NS4 0.959 Q32NS4 →
Q4R9A8 0.958 Q4R9A8 →
Q3MHJ2 0.957 Q3MHJ2 →
Q6PFJ9 0.957 Q6PFJ9 →
A0A2R8QFQ6 0.957 A0A2R8QFQ6 →
Q9Z1K5 0.956 Q9Z1K5 →
A2VEA3 0.956 A2VEA3 →
Q91854 0.956 Q91854 →
Q5SRY7 0.956 Q5SRY7 →
GLS Glutaminase kidney isoform, mitochondrial 0.956 landscape →
Q9Y4X5 0.955 Q9Y4X5 →
Q5F398 0.955 Q5F398 →
Q4VC33 0.954 Q4VC33 →
Q5R532 0.954 Q5R532 →
Q7L5Y9 0.954 Q7L5Y9 →
Q6GR10 0.953 Q6GR10 →
CDC16 Cell division cycle protein 16 homolog 0.953 landscape →
P13264 0.952 P13264 →
Q9UL63 0.951 Q9UL63 →
Q6NW85 0.951 Q6NW85 →
B1H1E4 0.951 B1H1E4 →
Q7SXR3 0.950 Q7SXR3 →
D3Z7P3 0.950 D3Z7P3 →
Q5RKJ1 0.950 Q5RKJ1 →