Sugi Predict
/ Targets
/ KIF18B
Top predicted compounds (top 20 by supporting neighbours, then confidence)
| Compound | Confidence | Supporting neighbours |
|---|
Clinical trials — most relevant to KIF18B by text similarity (a relevance ranking, not an exhaustive list)
| Trial | Phase | Status |
|---|
| A Study to Investigate Safety, Tolerability, Pharmacokinetics and Preliminary Efficacy With GenSci122 in Participants With Advanced Solid Tumors |
PHASE1 | RECRUITING |
| Phase I Study of Oral BAY 1217389 in Combination With Intravenous Paclitaxel |
PHASE1 | COMPLETED |
| Progressive Familial Intrahepatic Cholestasis in Indian Children - Establishing an Indian PFIC Registry |
nan | UNKNOWN |
| Biomarker Research in Inherited Movement Disorders |
nan | RECRUITING |
| Genetic Study of Patients With Primary Ciliary Dyskinesia |
nan | COMPLETED |
| Registry and Natural History of Epilepsy-Dyskinesia Syndromes |
nan | RECRUITING |
| Natural History Evaluation of Charcot Marie Tooth Disease (CMT) Types CMT1B, CMT2A, CMT4A, CMT4C, and Others |
nan | RECRUITING |
| Genetic Studies of Strabismus, Congenital Cranial Dysinnervation Disorders (CCDDs), and Their Associated Anomalies |
nan | RECRUITING |
| Classification, Functional Stratification and Biomarkers in Ciliopathy (CILLICORIRCM) |
nan | COMPLETED |
| Chromosome 18 Clinical Research Center |
nan | RECRUITING |
| Mapping Disease Pathways for Biliary Atresia |
nan | RECRUITING |
| Evaluation and Treatment of Pediatric, Developmental, and Genetic Eye Diseases |
nan | COMPLETED |
| Natural History Study of SLC25A46 Mutation-related Mitochondriopathy |
nan | COMPLETED |
| Delineating the Molecular Spectrum and the Clinical, Imaging and Neuronal Phenotype of Chopra-Amiel-Gordon Syndrome |
nan | RECRUITING |
| Genetics of Pediatric-Onset Motor Neuron and Neuromuscular Diseases |
nan | COMPLETED |
| Gait in Rare Diseases |
nan | COMPLETED |
| Assessing the Polygenic Burden of Rare Disruptive Mutations in Parkinson's Disease |
nan | UNKNOWN |
| Clinical Registry Investigating Bardet-Biedl Syndrome |
nan | RECRUITING |
| Long-read Genome Sequencing for the Molecular Diagnosis of Dystonia |
nan | RECRUITING |
| Exploring a Motor Learning Technique Based on the Mirror Motor Neuron System |
nan | COMPLETED |
| Better Delineation of CDK13 Related Phenotype and Epigenetic Signature. |
nan | UNKNOWN |
| PCD New Gene Discovery |
nan | COMPLETED |
| Integrated Model for Promoting Parenting and Early School Readiness in Pediatrics |
nan | COMPLETED |
| Pathogenesis of Primary Ciliary Dyskinesia (PCD) Lung Disease |
nan | RECRUITING |
| Pediatric Evaluation and Registry for Liver Cholestasis in Canada |
nan | RECRUITING |
| Investigating Phenotypic, Epigenetic, and NeuroGenetic Traits in Rare and Ultra-rare Neurodevelopmental Disorders (Project PENGUIN) |
nan | RECRUITING |
| Hong Kong Spinocerebellar Ataxias Registry |
nan | RECRUITING |
| iPSC Neurons From Adult Survivors of Childhood Cancer Who Have Persistent Vincristine-Induced Neuropathy |
nan | COMPLETED |
| Muscle Tissue Bank for Muscular Dystrophy |
nan | COMPLETED |
| Spastic Paraplegia - Centers of Excellence Research Network |
nan | RECRUITING |
Related proteins — ESM-2 sequence neighbours (a KIF18B binder may also engage these)