SEC22B

Vesicle-trafficking protein SEC22b · O75396 · SEC22B on Sugi Atlas →

0 patent compounds predicted against SEC22B, 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 SEC22B by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
CHED - Congenital Hereditary Endothelial Dystrophy: New Paradigm Shift in Therapy Using Topical Eye Drops PHASE2UNKNOWN
Ambroxol Therapy for Patients With Type 1 Gaucher Disease and Suboptimal Response to Enzyme Replacement Therapy PHASE2COMPLETED
Targeting Endoplasmic Reticulum Stress in Human Hypertension PHASE1/PHASE2RECRUITING
Melpida: Recombinant Adeno-associated Virus (serotype 9) Encoding a Codon Optimized Human AP4M1 Transgene (hAP4M1opt) PHASE1/PHASE2RECRUITING
Modulate Cellular Stress in the Immune Cells to Reduce Rate of Symptomatic Viral Infection PHASE2COMPLETED
Safety and Efficacy of AAV9/AP4B1 (BFB-101) For Patients With AP4B1-related Hereditary Spastic Paraplegia Type 47 (SPG47) PHASE1/PHASE2NOT_YET_RECRUITING
Phase I Study of Novel Estrogen Receptor(ER) a36 Modifier Icaritin in Advanced Breast Cancer Patients PHASE1UNKNOWN
PBA Use for Treatment of ATF6-/- Patients EARLY_PHASE1SUSPENDED
Surfactant Derived Protocol in Heart Failure nanCOMPLETED
Genetic Investigations in Children With Developmental and Epileptic Encephalopathies in Ho Chi Minh City, Vietnam nanUNKNOWN
Genetic Variation in TRAF3IP2 (rs13190932) nanRECRUITING
Pharmacogenomic Association Study in Indian Children With Acute Lymphoblastic Leukemia nanRECRUITING
Prevalence of a Non-Expressing 11B Mutation in Aka Peoples of the Central African Republic nanCOMPLETED
Hydroxychloroquin (HCQ) in chILD of Genetic Defect nanCOMPLETED
The Influence of Genetic Variations in ELAPOR1 or ELAPOR2 on Insulin Secretion and Glucose Regulation in Humans nanUNKNOWN
Study of Constitutional Platelet Disease nanUNKNOWN
Pathogenesis of Primary Ciliary Dyskinesia (PCD) Lung Disease nanRECRUITING
MERC Proteins in Saliva and GCF in Periodontal Disease (ELISA Study) nanCOMPLETED
MEHMO Natural History and Biomarkers nanRECRUITING
Fatty Acids Lipidome and Oxidative Stress in Liver Transplantation nanUNKNOWN
A Multicentric European Study to Promote Clinical Trial Readiness for STXBP1-related Disorders nanRECRUITING
Transcripts with Retained H/ACA Box SnoRNA Sequences As Biomarkers for Estrogen Dependence in Lum-B Breast Carcinomas nanACTIVE_NOT_RECRUITING
Phenotypic and Genotypic Characterization of Subjects With Syndromic Obesity: Identifying New Candidate Genes by Exome Sequencing (OBEXOME) nanCOMPLETED
The LD Lync Study - Natural History Study of Lipodystrophy Syndromes nanRECRUITING
Genetic Analysis of Gray Platelet Syndrome nanCOMPLETED
PREcision Diagnostics in Rare genetIC Diseases and Tumors - Long Read Sequencing nanRECRUITING
Establishment of Human Cellular Disease Models for Wilson Disease nanCOMPLETED
Mauriac Syndrome: Isotopic Techniques and Genetic Analysis nanCOMPLETED
Vitamin D Supplementation in Warfighters nanCOMPLETED
Identification and Characterization of Novel Non-Coding Variants That Contribute to Genetic Disorders nanCOMPLETED

Related proteins — ESM-2 sequence neighbours (a SEC22B binder may also engage these)

ProteinNameSimilarity
Q5ZJW4 1.000 Q5ZJW4 →
Q5RAI9 1.000 Q5RAI9 →
Q4KM74 1.000 Q4KM74 →
O08547 1.000 O08547 →
O08595 1.000 O08595 →
Q6P7L4 1.000 Q6P7L4 →
Q7SXP0 1.000 Q7SXP0 →
Q7ZV15 0.998 Q7ZV15 →
Q6C880 0.995 Q6C880 →
Q9Y7L0 0.994 Q9Y7L0 →
Q74ZD2 0.990 Q74ZD2 →
Q757A4 0.986 Q757A4 →
Q6CJA0 0.985 Q6CJA0 →
Q6CSA2 0.982 Q6CSA2 →
A0A423WHI6 0.981 A0A423WHI6 →
P36015 0.981 P36015 →
Q6FWT0 0.981 Q6FWT0 →
Q6BSL0 0.981 Q6BSL0 →
Q7ZUN8 0.979 Q7ZUN8 →
Q6FW27 0.979 Q6FW27 →
O60073 0.979 O60073 →
Q6C537 0.978 Q6C537 →
Q9LVM9 0.977 Q9LVM9 →
Q9LFP1 0.976 Q9LFP1 →
O15498 0.974 O15498 →
Q3T000 0.974 Q3T000 →
P22214 0.973 P22214 →
Q32N70 0.973 Q32N70 →
Q6DDU7 0.972 Q6DDU7 →
Q6P816 0.971 Q6P816 →