Sugi Predict

Sugi Predict / Targets / EXOC4

EXOC4

Exocyst complex component 4 · Q96A65 · EXOC4 on Sugi Atlas →

0 patent compounds predicted against EXOC4, 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 EXOC4 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Melpida: Recombinant Adeno-associated Virus (serotype 9) Encoding a Codon Optimized Human AP4M1 Transgene (hAP4M1opt) PHASE1/PHASE2RECRUITING
Functional Studies of Novel Genes Mutated in Primary Ciliary Dyskinesia II: Genotype to Phenotype EARLY_PHASE1COMPLETED
Study of the Pathophysiological Mechanisms Involved in Bleeding Events nanCOMPLETED
PCD New Gene Discovery nanCOMPLETED
Characterization of New Candidate Genes in Cases of Human Inherited Thrombocytopenia (CATCH) nanCOMPLETED
Study of Chediak-Higashi Syndrome nanRECRUITING
Thoracic Aortic Dilatation Syndromes nanCOMPLETED
Maternal Genes and Epimutations: Beckwith-Wiedemann Syndrome & Reproductive Risks nanRECRUITING
Classification, Functional Stratification and Biomarkers in Ciliopathy (CILLICORIRCM) nanCOMPLETED
Genetic Characterization of Parkinson's Disease nanCOMPLETED
Identification of Genetic Basis of Atrioventricular Conduction Defects: From Congenital Forms to Degenerative Forms nanUNKNOWN
Autophagy in Systemic Lupus Erythematosus nanUNKNOWN
Diagnosis of Primary Ciliary Dyskinesia nanCOMPLETED
Pathogenesis of Primary Ciliary Dyskinesia (PCD) Lung Disease nanRECRUITING
Exome Analysis in Hearing Impaired Patients nanUNKNOWN
Mapping Disease Pathways for Biliary Atresia nanRECRUITING
Monogenic Diabetes Misdiagnosed as Type 1 nanRECRUITING
Whole Exome and Whole Genome Sequencing for Genotyping of Inherited and Congenital Eye Conditions nanRECRUITING
Next Generation to Identify Genetic Causes of Disease in Patients Participating in NICHD Clinical Protocols nanCOMPLETED
Genetics of Primary Ciliary Dyskinesia nanCOMPLETED
Genetic Variations That Increase the Risk for Calcium Kidney Stones: a Family-based Study nanCOMPLETED
EXtremely Early-onset Type 1 Diabetes EXtremely Early-onset Type 1 Diabetes (A Musketeers' Memorandum Study) nanRECRUITING
Multicentric Prospective Study of Genetic and Physiopathology Concerning Dysregulation of Complement During Repeated Fetal Abortions nanCOMPLETED
The Influence of Genetic Variations in ELAPOR1 or ELAPOR2 on Insulin Secretion and Glucose Regulation in Humans nanUNKNOWN
Genetic Investigation of Cancer Predisposition nanNOT_YET_RECRUITING
Williams Syndrome (WS) and Supravalvar Aortic Stenosis (SVAS) DNA and Tissue Bank nanCOMPLETED
A Study of Circulating Exosome Proteomics In Gallbladder Carcinoma Patients nanUNKNOWN
Identification of a New Gene Involved in Hereditary Lipodystrophy nanCOMPLETED
Pharmacogenomic Association Study in Indian Children With Acute Lymphoblastic Leukemia nanRECRUITING
Whole Exome Sequencing in Coronary Artery Ectasia nanCOMPLETED

Related proteins — ESM-2 sequence neighbours (a EXOC4 binder may also engage these)

ProteinNameSimilarity
O35382 — 1.000 O35382 →
Q62824 — 1.000 Q62824 →
Q5SPW0 — 0.983 Q5SPW0 →
Q9P1Q0 — 0.981 Q9P1Q0 →
Q9JMK8 — 0.977 Q9JMK8 →
Q8R313 — 0.975 Q8R313 →
Q155U0 — 0.974 Q155U0 →
Q8R1U1 — 0.971 Q8R1U1 →
Q5R7R6 — 0.968 Q5R7R6 →
Q9R1D7 — 0.968 Q9R1D7 →
Q3MHG0 — 0.967 Q3MHG0 →
Q84K25 — 0.967 Q84K25 →
Q5RAQ5 — 0.966 Q5RAQ5 →
Q91W96 — 0.965 Q91W96 →
Q9D4H1 — 0.964 Q9D4H1 →
Q96KP1 — 0.964 Q96KP1 →
O54923 — 0.964 O54923 →
COG4 Conserved oligomeric Golgi complex subunit 4 0.964 landscape →
O54921 — 0.963 O54921 →
Q8N960 — 0.962 Q8N960 →
A0JN62 — 0.962 A0JN62 →
Q9D4F8 — 0.962 Q9D4F8 →
TUBGCP4 Gamma-tubulin complex component 4 0.962 landscape →
Q5ZJA9 — 0.961 Q5ZJA9 →
Q8K3H0 — 0.961 Q8K3H0 →
Q8CCB4 — 0.961 Q8CCB4 →
Q9UKG1 — 0.961 Q9UKG1 →
Q92538 — 0.961 Q92538 →
E2R766 — 0.960 E2R766 →
Q9UJX5 — 0.960 Q9UJX5 →