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Sugi Predict / Targets / WDR91

WDR91

WD repeat-containing protein 91 · A4D1P6 · WDR91 on Sugi Atlas →

1,320 patent compounds predicted against WDR91, 440 high-confidence (nearest known ligand ≥ 0.5)

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

CompoundConfidenceSupporting neighbours
SCHEMBL22685351 SCHEMBL22685351 0.54 12/20
SCHEMBL22685311 SCHEMBL22685311 0.55 11/20
SCHEMBL22685198 SCHEMBL22685198 0.53 11/20
SCHEMBL22685078 SCHEMBL22685078 0.53 11/20
SCHEMBL22684760 SCHEMBL22684760 0.53 10/20
SCHEMBL22438959 SCHEMBL22438959 0.57 7/20
SCHEMBL23908270 SCHEMBL23908270 0.56 7/20
SCHEMBL20898400 SCHEMBL20898400 0.54 7/20
SCHEMBL6121880 SCHEMBL6121880 0.39 7/20
SCHEMBL22439026 SCHEMBL22439026 0.41 6/20
SCHEMBL16249346 SCHEMBL16249346 0.53 5/20
SCHEMBL14879488 SCHEMBL14879488 0.50 5/20
SCHEMBL26373089 SCHEMBL26373089 0.43 5/20
SCHEMBL22685074 SCHEMBL22685074 0.42 5/20
SCHEMBL26674453 SCHEMBL26674453 0.40 5/20
SCHEMBL19343136 SCHEMBL19343136 0.37 5/20
SCHEMBL19343498 SCHEMBL19343498 0.36 5/20
SCHEMBL30339572 SCHEMBL30339572 0.36 5/20
SCHEMBL9106437 SCHEMBL9106437 0.59 4/20
SCHEMBL16695637 SCHEMBL16695637 0.59 4/20

Clinical trials — most relevant to WDR91 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Cornelia De Lange Syndrome: Assessing Positive Effects of Lithium Treatment PHASE2/PHASE3RECRUITING
Gene Therapy for Wiskott-Aldrich Syndrome PHASE1/PHASE2COMPLETED
Characterization of WAGR Syndrome and Other Chromosome 11 Gene Deletions nanCOMPLETED
Whole-genome Sequencing Study in Patients With Diminished Ovarian Reserve nanUNKNOWN
Genetics of Endocrine Tumours - Familial Isolated Pituitary Adenoma - FIPA nanRECRUITING
Delineating the Molecular Spectrum and the Clinical, Imaging and Neuronal Phenotype of Chopra-Amiel-Gordon Syndrome 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
Classification, Functional Stratification and Biomarkers in Ciliopathy (CILLICORIRCM) nanCOMPLETED
Human Epilepsy Genetics--Neuronal Migration Disorders Study nanRECRUITING
Genetic Characterization of Parkinson's Disease nanCOMPLETED
PCD New Gene Discovery nanCOMPLETED
PHF19 Gene Expression and EZH2 Gene Deletion in Acute Myeloid Leukemia nanUNKNOWN
Better Delineation of DDX3X Related Phenotype and Epigenetic Signature. nanUNKNOWN
Study of a Candidate Gene Involved in Goldenhar Syndrome. nanCOMPLETED
Natural History and Genetic Studies of Usher Syndrome nanCOMPLETED
MEHMO Natural History and Biomarkers nanRECRUITING
Characterization of New Candidate Genes in Cases of Human Inherited Thrombocytopenia (CATCH) nanCOMPLETED
Exome Sequencing Study in Cardiomyopathy to Identify New Risk Variants nanUNKNOWN
Molecular Diagnosis of Syndromic or Isolated Severe Intellectual Disability Using Whole Exome Sequencing : a Pilot Study nanCOMPLETED
Identifying Genes and Mutations Underlying Retinitis Pigmentosa and Allied Diseases nanUNKNOWN
Maternal Genes and Epimutations: Beckwith-Wiedemann Syndrome & Reproductive Risks nanRECRUITING
Identification of the Genetic Causes of Rare Diseases With Negative Exome Findings nanUNKNOWN
Genetic Analyses of Nonsyndromic and Syndromic Deafness in Pakistan nanENROLLING_BY_INVITATION
Study to Investigate Genetic Causes of Severe Early Childhood Onset Obesity. nanRECRUITING
Aberrant Splicings Due to Microsatellite Instability in Colorectal Cancer : Physiopathological and Clinical Impact nanUNKNOWN
Williams Syndrome (WS) and Supravalvar Aortic Stenosis (SVAS) DNA and Tissue Bank nanCOMPLETED
Identification of Genetic Factors Implicated in Orofacial Cleft Using Whole Exome Sequencing nanRECRUITING
Genetic Study of Patients With Primary Ciliary Dyskinesia nanCOMPLETED
Genetics and Psychopathology in the 22q11 Deletion Syndrome nanUNKNOWN

Related proteins — ESM-2 sequence neighbours (a WDR91 binder may also engage these)

ProteinNameSimilarity
Q2HJE1 — 1.000 Q2HJE1 →
Q7TMQ7 — 1.000 Q7TMQ7 →
Q6TEN6 — 1.000 Q6TEN6 →
Q5ZLL7 — 1.000 Q5ZLL7 →
Q5R6T6 — 1.000 Q5R6T6 →
B2RYI0 — 1.000 B2RYI0 →
Q05B30 — 0.999 Q05B30 →
A0A2R8QPS5 — 0.996 A0A2R8QPS5 →
Q1LUT1 — 0.996 Q1LUT1 →
Q7Z3E5 — 0.995 Q7Z3E5 →
Q8TDY4 — 0.995 Q8TDY4 →
Q4V9P9 — 0.994 Q4V9P9 →
Q9Y3R5 — 0.994 Q9Y3R5 →
Q9VKK2 — 0.994 Q9VKK2 →
Q5PQS3 — 0.994 Q5PQS3 →
Q27GK7 — 0.994 Q27GK7 →
Q8BX57 — 0.994 Q8BX57 →
Q8WUM0 — 0.994 Q8WUM0 →
O17468 — 0.994 O17468 →
Q99KY4 — 0.994 Q99KY4 →
Q3UMY5 — 0.993 Q3UMY5 →
Q5NBT9 — 0.993 Q5NBT9 →
Q14D04 — 0.993 Q14D04 →
A9JRI0 — 0.993 A9JRI0 →
Q84JM4 — 0.993 Q84JM4 →
P25799 — 0.993 P25799 →
A1A5P5 — 0.993 A1A5P5 →
Q9NQW1 — 0.993 Q9NQW1 →
Q7Z401 — 0.992 Q7Z401 →
A8E7C5 — 0.992 A8E7C5 →