Sugi Predict
/ Targets
/ KIF2C
Top predicted compounds (top 20 by supporting neighbours, then confidence)
| Compound | Confidence | Supporting neighbours |
|---|
Clinical trials — most relevant to KIF2C by text similarity (a relevance ranking, not an exhaustive list)
| Trial | Phase | Status |
|---|
| Vinorelbine in Relapsed Platinum Resistant or Refractory C5 High Grade Serous, Endometrioid, or Undifferentiated Primary Peritoneum, Fallopian Tube or Ovarian Cancer |
PHASE2 | UNKNOWN |
| Functional Studies of Novel Genes Mutated in Primary Ciliary Dyskinesia II: Genotype to Phenotype |
EARLY_PHASE1 | COMPLETED |
| Genetic Study of Patients With Primary Ciliary Dyskinesia |
nan | COMPLETED |
| Biomarker Research in Inherited Movement Disorders |
nan | RECRUITING |
| Investigation of the Genetic Causes of Kallmann Syndrome and Reproductive Disorders |
nan | COMPLETED |
| Classification, Functional Stratification and Biomarkers in Ciliopathy (CILLICORIRCM) |
nan | COMPLETED |
| Core Stability Exercises and Hereditary Ataxia |
nan | COMPLETED |
| Pediatric Evaluation and Registry for Liver Cholestasis in Canada |
nan | RECRUITING |
| Delineating the Molecular Spectrum and the Clinical, Imaging and Neuronal Phenotype of Chopra-Amiel-Gordon Syndrome |
nan | RECRUITING |
| Gait in Rare Diseases |
nan | COMPLETED |
| Registry and Natural History of Epilepsy-Dyskinesia Syndromes |
nan | RECRUITING |
| Clinical Registry Investigating Bardet-Biedl Syndrome |
nan | RECRUITING |
| Mapping Disease Pathways for Biliary Atresia |
nan | RECRUITING |
| Genetic Studies of Strabismus, Congenital Cranial Dysinnervation Disorders (CCDDs), and Their Associated Anomalies |
nan | RECRUITING |
| Natural History Evaluation of Charcot Marie Tooth Disease (CMT) Types CMT1B, CMT2A, CMT4A, CMT4C, and Others |
nan | RECRUITING |
| Integrated Model for Promoting Parenting and Early School Readiness in Pediatrics |
nan | COMPLETED |
| Genetics of Pediatric-Onset Motor Neuron and Neuromuscular Diseases |
nan | COMPLETED |
| Evaluation and Treatment of Pediatric, Developmental, and Genetic Eye Diseases |
nan | COMPLETED |
| Genetics of Primary Ciliary Dyskinesia |
nan | COMPLETED |
| Spastic Paraplegia - Centers of Excellence Research Network |
nan | RECRUITING |
| Exploring a Motor Learning Technique Based on the Mirror Motor Neuron System |
nan | COMPLETED |
| Investigating Phenotypic, Epigenetic, and NeuroGenetic Traits in Rare and Ultra-rare Neurodevelopmental Disorders (Project PENGUIN) |
nan | RECRUITING |
| Structural Validity and Inter-rater Reliabitiliy of the Ataxia Trunk, Lower And Upper Extremity Scale (ATLAS) |
nan | NOT_YET_RECRUITING |
| Result Of Karyotyping in Pediatric Patients With Congenital Anomalies and Developmental Delay |
nan | NOT_YET_RECRUITING |
| PCD New Gene Discovery |
nan | COMPLETED |
| Hereditary Spastic Paraplegia Genomic Sequencing Initiative (HSPseq) |
nan | RECRUITING |
| Diagnosis of Primary Ciliary Dyskinesia |
nan | COMPLETED |
| Neurogenetics Patient Registry |
nan | RECRUITING |
| Pathogenesis of Primary Ciliary Dyskinesia (PCD) Lung Disease |
nan | RECRUITING |
| Long-read Genome Sequencing for the Molecular Diagnosis of Dystonia |
nan | RECRUITING |
Related proteins — ESM-2 sequence neighbours (a KIF2C binder may also engage these)