FMNL1

Formin-like protein 1 · O95466 · FMNL1 on Sugi Atlas →

0 patent compounds predicted against FMNL1, 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 FMNL1 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Biologic Correlative Taxotere/AC PHASE2COMPLETED
Investigator-initiated Clinical Trial of MIKE-1 PHASE1/PHASE2UNKNOWN
Scleral Buckling for Retinal Detachment Prevention in Genetically Confirmed Stickler Syndrome PHASE2WITHDRAWN
Molecular Analysis of Patients With Neuromuscular Disease nanRECRUITING
Significance of Immunohistochemical Expression of Fascin-1 in Colorectal Carcinoma nanCOMPLETED
Family Blood Pressure Program - GenNet Network nanCOMPLETED
Cardiopulmonary and Right Ventricular Function in Health and Disease nanUNKNOWN
Muscle Tissue Bank for Muscular Dystrophy nanCOMPLETED
Mapping Novel Disease Genes for Dilated Cardiomyopathy nanCOMPLETED
Family Blood Pressure Program - SAPPHIRe Network nanCOMPLETED
Skeletal Muscle Regeneration in Survivors of Critical Illness: How to Prevent Satellite Cell Failure? nanRECRUITING
Family Blood Pressure Program - HyperGEN nanCOMPLETED
Family Blood Pressure Program - GENOA nanCOMPLETED
Identification of New FTLD Genes nanUNKNOWN
Gene Mutations and Rescue in Human Congenital Diaphragmatic Hernia nanUNKNOWN
Genetic Characterization of Parkinson's Disease nanCOMPLETED
Familial Partial Lipodystrophy Study nanCOMPLETED
Magnetic Resonance Imaging (MRI) of Neuropsychiatric Patients and Healthy Volunteers nanCOMPLETED
FGL2/Fibroleukin and Hepatitis C Virus Recurrence Post Liver Transplantation nanUNKNOWN
Shanghai High Myopia Study nanRECRUITING
Dynamics of Muscle Mitochondria in Type 2 Diabetes Exercise nanCOMPLETED
HYPOCHOL : A Genetically-based Strategy to Identify New Targets in Cholesterol Metabolism nanACTIVE_NOT_RECRUITING
Role of Genetics in Idiopathic Pulmonary Fibrosis (IPF) nanUNKNOWN
Clubfoot DNA Repository nanCOMPLETED
Molecular and Genetic Studies of Congenital Myopathies nanRECRUITING
Predicting Postoperative Delirium Using EEG, Genetics and Neurobiomarkers of Cerebral Injury nanCOMPLETED
Autophagy in Systemic Lupus Erythematosus nanUNKNOWN
Genetic Studies of Strabismus, Congenital Cranial Dysinnervation Disorders (CCDDs), and Their Associated Anomalies nanRECRUITING
Thoracic Aortic Dilatation Syndromes nanCOMPLETED
Proteomic Study of Tears From Patients With a PAX6 Mutation nanCOMPLETED

Related proteins — ESM-2 sequence neighbours (a FMNL1 binder may also engage these)

ProteinNameSimilarity
Q9JL26 1.000 Q9JL26 →
Q86T65 0.995 Q86T65 →
Q9Y4D1 0.989 Q9Y4D1 →
Q8BPM0 0.989 Q8BPM0 →
Q6ZPF4 0.989 Q6ZPF4 →
Q6NXC0 0.989 Q6NXC0 →
Q80U19 0.989 Q80U19 →
Q8IVF7 0.988 Q8IVF7 →
B0DOB5 0.988 B0DOB5 →
F1M775 0.987 F1M775 →
Q9Y613 0.987 Q9Y613 →
O08808 0.987 O08808 →
DIAPH1 Protein diaphanous homolog 1 0.987 landscape →
A2APV2 0.987 A2APV2 →
A0A1D5P556 0.986 A0A1D5P556 →
Q66K14 0.984 Q66K14 →
O15068 0.984 O15068 →
Q9UJY5 0.983 Q9UJY5 →
NR1H2 Oxysterols receptor LXR-beta 0.982 landscape →
Q96PY5 0.982 Q96PY5 →
Q9VUC6 0.982 Q9VUC6 →
PTK2B Protein-tyrosine kinase 2-beta 0.982 landscape →
GAK Cyclin-G-associated kinase 0.982 landscape →
Q9CSU0 0.982 Q9CSU0 →
O15013 0.982 O15013 →
Q9H1H9 0.982 Q9H1H9 →
Q63406 0.982 Q63406 →
A0A3Q1LSX9 0.982 A0A3Q1LSX9 →
Q92619 0.982 Q92619 →
Q15027 0.982 Q15027 →