WDR36

WD repeat-containing protein 36 · Q8NI36 · WDR36 on Sugi Atlas →

0 patent compounds predicted against WDR36, 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 WDR36 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Whole-genome Sequencing Study in Patients With Diminished Ovarian Reserve nanUNKNOWN
Delineating the Molecular Spectrum and the Clinical, Imaging and Neuronal Phenotype of Chopra-Amiel-Gordon Syndrome nanRECRUITING
MEHMO Natural History and Biomarkers nanRECRUITING
The Phenotyping and Genotyping of Taiwanese Patients With Obstructive Sleep Apnea nanUNKNOWN
Application of Linkage Analysis in the Identification of Novel Hereditary Factors in Familial Aneurysms nanACTIVE_NOT_RECRUITING
Characterization of WAGR Syndrome and Other Chromosome 11 Gene Deletions nanCOMPLETED
Characterization of New Candidate Genes in Cases of Human Inherited Thrombocytopenia (CATCH) nanCOMPLETED
Better Delineation of DDX3X Related Phenotype and Epigenetic Signature. nanUNKNOWN
Better Delineation of CDK13 Related Phenotype and Epigenetic Signature. nanUNKNOWN
Markers and Mechanisms of Macrovascular Disease in IDDM nanCOMPLETED
Study of a Candidate Gene Involved in Goldenhar Syndrome. nanCOMPLETED
Maternal Genes and Epimutations: Beckwith-Wiedemann Syndrome & Reproductive Risks nanRECRUITING
Molecular Diagnosis of Syndromic or Isolated Severe Intellectual Disability Using Whole Exome Sequencing : a Pilot Study nanCOMPLETED
Microarray Analysis in Syndromic Obesity nanCOMPLETED
Impact of Elastin Mediated Vascular Stiffness on End Organs nanCOMPLETED
Identification of the Genetic Causes of Rare Diseases With Negative Exome Findings nanUNKNOWN
Classification, Functional Stratification and Biomarkers in Ciliopathy (CILLICORIRCM) nanCOMPLETED
Study to Investigate Genetic Causes of Severe Early Childhood Onset Obesity. nanRECRUITING
Genetic Characterization of Parkinson's Disease nanCOMPLETED
PCD New Gene Discovery nanCOMPLETED
Autophagy in Systemic Lupus Erythematosus nanUNKNOWN
Exploring Novel Biomarkers of ICU-AW in Mechanically Ventilated Children at the Molecular Level nanENROLLING_BY_INVITATION
Shwachman Diamond Syndrome Registry and Study nanRECRUITING
Child Development and Genetic Biomarkers(II): Gene Verification and Data Integration nanUNKNOWN
Whole Genome Scan of Extended Families With Familial Vocal Cord Paralysis nanCOMPLETED
Whole Exome and Whole Genome Sequencing for Genotyping of Inherited and Congenital Eye Conditions nanRECRUITING
Genetics of Primary Ciliary Dyskinesia nanCOMPLETED
Natural History and Genetic Studies of Usher Syndrome nanCOMPLETED
Genetic Study of Patients With Primary Ciliary Dyskinesia nanCOMPLETED
Genetic and Physical Characteristics of Rett Syndrome nanCOMPLETED

Related proteins — ESM-2 sequence neighbours (a WDR36 binder may also engage these)

ProteinNameSimilarity
Q68EI0 0.980 Q68EI0 →
PLAA Phospholipase A-2-activating protein 0.978 landscape →
Q96MR6 0.976 Q96MR6 →
Q9Y484 0.975 Q9Y484 →
Q6DCV0 0.975 Q6DCV0 →
Q9P2H3 0.975 Q9P2H3 →
P27612 0.975 P27612 →
Q8K057 0.974 Q8K057 →
Q9CWF6 0.974 Q9CWF6 →
Q496Z0 0.974 Q496Z0 →
Q3UR70 0.974 Q3UR70 →
E7F590 0.974 E7F590 →
Q91VM3 0.974 Q91VM3 →
Q9BXC9 0.974 Q9BXC9 →
E9PY46 0.973 E9PY46 →
Q3UGF1 0.973 Q3UGF1 →
O00423 0.973 O00423 →
Q66HB3 0.973 Q66HB3 →
Q68F45 0.973 Q68F45 →
Q8WUH2 0.973 Q8WUH2 →
MAP4K5 Mitogen-activated protein kinase kinase kinase kinase 5 0.973 landscape →
Q9CR39 0.972 Q9CR39 →
F4IDS7 0.972 F4IDS7 →
Q920Q4 0.972 Q920Q4 →
Q7ZUX3 0.972 Q7ZUX3 →
Q7ZUW6 0.972 Q7ZUW6 →
Q91WG4 0.971 Q91WG4 →
A0A1L8HX76 0.971 A0A1L8HX76 →
P54319 0.971 P54319 →
Q8BPM2 0.971 Q8BPM2 →