Sugi Predict

Sugi Predict / Targets / WDR12

WDR12

Ribosome biogenesis protein WDR12 · Q9GZL7 · WDR12 on Sugi Atlas →

0 patent compounds predicted against WDR12, 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 WDR12 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Assessing the Safety, Tolerability, and Efficacy of APR-2020 in Pediatric and Adolescent Subjects With RPS19 Deficient Diamond-Blackfan Anemia PHASE1RECRUITING
Temsirolimus and Sorafenib in Advanced Hepatocellular Carcinoma PHASE1COMPLETED
Whole-genome Sequencing Study in Patients With Diminished Ovarian Reserve nanUNKNOWN
Better Delineation of CDK13 Related Phenotype and Epigenetic Signature. nanUNKNOWN
MEHMO Natural History and Biomarkers nanRECRUITING
Child Development and Genetic Biomarkers(II): Gene Verification and Data Integration nanUNKNOWN
Characterization of WAGR Syndrome and Other Chromosome 11 Gene Deletions nanCOMPLETED
Study to Investigate Genetic Causes of Severe Early Childhood Onset Obesity. nanRECRUITING
Classification, Functional Stratification and Biomarkers in Ciliopathy (CILLICORIRCM) nanCOMPLETED
Characterization of Angelman Syndrome nanCOMPLETED
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
Delineating the Molecular Spectrum and the Clinical, Imaging and Neuronal Phenotype of Chopra-Amiel-Gordon Syndrome nanRECRUITING
Identification of the Genetic Causes of Rare Diseases With Negative Exome Findings nanUNKNOWN
Aberrant Splicings Due to Microsatellite Instability in Colorectal Cancer : Physiopathological and Clinical Impact nanUNKNOWN
Genomic Medicine for Ill Neonates and Infants (The GEMINI Study) nanCOMPLETED
Inbon Errors of Immunity Attending Assiut University Children&Amp;#39;s Hospital: a Single Center Study nanNOT_YET_RECRUITING
UW Undiagnosed Genetic Diseases Program nanRECRUITING
Genetic Study of Patients With Primary Ciliary Dyskinesia nanCOMPLETED
Study of a Candidate Gene Involved in Goldenhar Syndrome. nanCOMPLETED
Angelman Syndrome Natural History Study nanRECRUITING
Phenotypic and Genotypic Characterization of Subjects With Syndromic Obesity: Identifying New Candidate Genes by Exome Sequencing (OBEXOME) nanCOMPLETED
Development of an Optimal Approach to Return of Results for Next-generation Sequencing for Prenatal Diagnosis nanWITHDRAWN
Genetic and Physical Characteristics of Rett Syndrome nanCOMPLETED
The Belgian Genome Resource to Resolve Rare Diseases nanCOMPLETED
Decoding Developmental Disorders in Humams nanCOMPLETED
Genetics of Endocrine Tumours - Familial Isolated Pituitary Adenoma - FIPA nanRECRUITING
Shwachman Diamond Syndrome Registry and Study nanRECRUITING
Identification of Genetic Factors Implicated in Orofacial Cleft Using Whole Exome Sequencing nanRECRUITING
A Retrospective and Prospective Natural History Study of Patients With WHIM Syndrome nanWITHDRAWN
Maternal Genes and Epimutations: Beckwith-Wiedemann Syndrome & Reproductive Risks nanRECRUITING

Related proteins — ESM-2 sequence neighbours (a WDR12 binder may also engage these)

ProteinNameSimilarity
P61480 — 1.000 P61480 →
Q5REE6 — 1.000 Q5REE6 →
Q0VC24 — 1.000 Q0VC24 →
B4GT01 — 1.000 B4GT01 →
B4JPT9 — 0.999 B4JPT9 →
B4P116 — 0.998 B4P116 →
Q6NX08 — 0.998 Q6NX08 →
B4KKN1 — 0.998 B4KKN1 →
A7RHG8 — 0.997 A7RHG8 →
Q9JJA4 — 0.997 Q9JJA4 →
Q5BJ90 — 0.997 Q5BJ90 →
B4LS78 — 0.997 B4LS78 →
Q7QJ33 — 0.996 Q7QJ33 →
B4MU54 — 0.994 B4MU54 →
B3MJV8 — 0.993 B3MJV8 →
B5DG67 — 0.993 B5DG67 →
B4HWV6 — 0.992 B4HWV6 →
B0W517 — 0.991 B0W517 →
Q29KQ0 — 0.990 Q29KQ0 →
Q9VKQ3 — 0.990 Q9VKQ3 →
Q17BB0 — 0.989 Q17BB0 →
A8QB65 — 0.989 A8QB65 →
B3N534 — 0.989 B3N534 →
B4Q9T6 — 0.989 B4Q9T6 →
B7PY76 — 0.988 B7PY76 →
Q8H594 — 0.987 Q8H594 →
Q756D0 — 0.986 Q756D0 →
Q9LF27 — 0.985 Q9LF27 →
Q40687 — 0.985 Q40687 →
F4I241 — 0.985 F4I241 →