SEPTIN8

Septin-8 · Q92599 · SEPTIN8 on Sugi Atlas →

0 patent compounds predicted against SEPTIN8, 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 SEPTIN8 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Phenoxybenzamine Versus Doxazosin in PCC Patients PHASE4COMPLETED
Treatment With HMG-COA Reductase Inhibitor of Growth and Bone Abnormalities in Children With Noonan Syndrome PHASE3COMPLETED
Circulating Cell-free DNA-based Epigenetic Biomarker mSEPT9 for Hepatocellular Carcinoma Detection in Cirrhosis nanCOMPLETED
HCCBloodTest for Detection of Hepatocellular Carcinoma (HCC) nanCOMPLETED
Assessing the Effect of a Blood-based Colorectal Cancer Screening Test on Screening Adherence and Colonoscopy Completion nanCOMPLETED
Addressing Colorectal Cancer in South Florida Firefighters nanCOMPLETED
Dissect Assembly Rules of SPET12 Complex in the Mammalian Sperm nanCOMPLETED
Understanding Patient Preference on Colorectal Cancer Screening Options-PSU nanCOMPLETED
Identification of New Colorectal Cancer Genes nanCOMPLETED
Exploratory Study of Rectal Mucus for Diagnosing Disease nanCOMPLETED
RNA Assays for Endometriosis Detection and Diagnosis nanENROLLING_BY_INVITATION
Role of Geminin and Mcm-2 in Prognosis of Renal Cell Carcinoma nanUNKNOWN
Molecular Genetics Study of Nasopharyngeal Carcinoma: Characterization of NCP Susceptibility Gene(s) nanCOMPLETED
Structural and Functional Connectivity in Autism Spectrum Disorders nanCOMPLETED
Genetics of Endocrine Tumours - Familial Isolated Pituitary Adenoma - FIPA nanRECRUITING
Mapping Novel Disease Genes for Dilated Cardiomyopathy nanCOMPLETED
Family Blood Pressure Program - GENOA nanCOMPLETED
Family Blood Pressure Program - SAPPHIRe Network nanCOMPLETED
Transcriptomic Profile of Patients Treated With Different Modalities of Spinal Cord Stimulation nanUNKNOWN
Genetic Basis of Abdominal Aortic Aneurysm nanCOMPLETED
A Prospective Study of Molecular Detection of Salvageable Early Recurrent Nasopharyngeal Carcinoma After Radiotherapy nanCOMPLETED
Genetic Identification (ID) of Segmental Dysplastic Nevi nanWITHDRAWN
Analysis of the Genotype/Phenotype Relationship in the Fuchs' Corneal Endothelial Dystrophy in France nanRECRUITING
Chromosome 5Q Gene Variants and Asthma-Related Traits nanCOMPLETED
Whole Genome Scan of Extended Families With Familial Vocal Cord Paralysis nanCOMPLETED
Gait in Rare Diseases nanCOMPLETED
Prospective Study of Molecular Predictors of Survival in Myelodysplastic Syndromes nanCOMPLETED
Investigation of the Genetic Causes of Kallmann Syndrome and Reproductive Disorders nanCOMPLETED
Phenotypic and Genotypic Studies in Congenital and Early Onset Ataxias nanCOMPLETED
Aberrant Splicings Due to Microsatellite Instability in Colorectal Cancer : Physiopathological and Clinical Impact nanUNKNOWN

Related proteins — ESM-2 sequence neighbours (a SEPTIN8 binder may also engage these)

ProteinNameSimilarity
Q9R1T4 1.000 Q9R1T4 →
B2KIE9 1.000 B2KIE9 →
O43236 1.000 O43236 →
Q8C1B7 1.000 Q8C1B7 →
Q2KJB1 0.999 Q2KJB1 →
P40797 0.999 P40797 →
B1MTN8 0.999 B1MTN8 →
Q8CHH9 0.998 Q8CHH9 →
Q6IRQ5 0.998 Q6IRQ5 →
SEPTIN6 Septin-6 0.998 landscape →
Q9P0V9 0.997 Q9P0V9 →
Q6AXA6 0.997 Q6AXA6 →
B1H120 0.997 B1H120 →
A4UUI3 0.997 A4UUI3 →
Q0VCP4 0.997 Q0VCP4 →
B5FW69 0.996 B5FW69 →
Q8C650 0.996 Q8C650 →
Q5REG8 0.996 Q5REG8 →
B3GNI6 0.995 B3GNI6 →
A0A3Q0KDV9 0.995 A0A3Q0KDV9 →
A0A096MJN4 0.995 A0A096MJN4 →
B0BNF1 0.995 B0BNF1 →
A8WSU9 0.994 A8WSU9 →
Q5PQK1 0.994 Q5PQK1 →
P54359 0.994 P54359 →
A4RKC3 0.994 A4RKC3 →
Q642H3 0.994 Q642H3 →
B0KWP7 0.994 B0KWP7 →
P39827 0.993 P39827 →
Q5ZMH1 0.993 Q5ZMH1 →