SNAPC4

snRNA-activating protein complex subunit 4 · Q5SXM2 · SNAPC4 on Sugi Atlas →

0 patent compounds predicted against SNAPC4, 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 SNAPC4 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Ketamine Treatment Effects on Synaptic Plasticity in Depression PHASE4COMPLETED
CMP-MYTHiC Trial and Registry - CardioMyoPathy With MYocarditis THerapy With Colchicine PHASE3RECRUITING
Melpida: Recombinant Adeno-associated Virus (serotype 9) Encoding a Codon Optimized Human AP4M1 Transgene (hAP4M1opt) PHASE1/PHASE2RECRUITING
Treatment of Temporo-Myofascial Disorder of Muscular Origin Using Botulinum Toxin: A Prospective Study PHASE2UNKNOWN
Safety and Efficacy of AAV9/AP4B1 (BFB-101) For Patients With AP4B1-related Hereditary Spastic Paraplegia Type 47 (SPG47) PHASE1/PHASE2NOT_YET_RECRUITING
Phenylbutyrate for Monogenetic Developmental and Epileptic Encephalopathy EARLY_PHASE1ACTIVE_NOT_RECRUITING
SNAP: Measurement of the Subjective Perception of the Symptom in Hereditary Spastic Paraparesis (HSP) nanCOMPLETED
Susceptibility Genes in Autism Spectrum Disorders nanCOMPLETED
Genetic Characterization of Parkinson's Disease nanCOMPLETED
Mechanisms of Cell Death in Spinal Muscular Atrophy nanCOMPLETED
Investigating Phenotypic, Epigenetic, and NeuroGenetic Traits in Rare and Ultra-rare Neurodevelopmental Disorders (Project PENGUIN) nanRECRUITING
Study of the Genetic Factors Involved in Autism and Related Disorders nanRECRUITING
Role of SF3B1 Mutation in Assessment of Acute and Chronic Lymphatic Leukemia nanNOT_YET_RECRUITING
Biomarker Research in Inherited Movement Disorders nanRECRUITING
Genetic Variants Associated With Adolescent Suicide Attempts nanCOMPLETED
Natural History Study of Smith-Magenis Syndrome nanACTIVE_NOT_RECRUITING
Thermogenic Silencer Regulatory Factors in Humans nanACTIVE_NOT_RECRUITING
Investigations Into ISCU Myopathy or Iron Sulfur Scaffold U Protein Myopathy nanCOMPLETED
Muscle Tissue Bank for Muscular Dystrophy nanCOMPLETED
Signs and Symptoms of Genetic Abnormalities Linked to Inherited Heart Disease nanCOMPLETED
Gene-STEPS: Shortening Time of Evaluation in Paediatric Epilepsy Services nanUNKNOWN
Role of Sorcin and Annexin A3 in Breast Cancer Patients nanUNKNOWN
Identifying Genes and Mutations Underlying Retinitis Pigmentosa and Allied Diseases nanUNKNOWN
Regulation of Lymphocyte Anti-tumor Response in Metastatic Patients Treated With the mTOR Inhibitor Everolimus nanCOMPLETED
Identification of New FTLD Genes nanUNKNOWN
Natural History Evaluation of Charcot Marie Tooth Disease (CMT) Types CMT1B, CMT2A, CMT4A, CMT4C, and Others nanRECRUITING
Pharmacogenomic Association Study in Indian Children With Acute Lymphoblastic Leukemia nanRECRUITING
Autophagy in Systemic Lupus Erythematosus nanUNKNOWN
Exploring the Genetics of Neuropathic Pain nanRECRUITING
Rolandic Epilepsy Genomewide Association International Study nanCOMPLETED

Related proteins — ESM-2 sequence neighbours (a SNAPC4 binder may also engage these)

ProteinNameSimilarity
Q8BP86 0.995 Q8BP86 →
A0JPN4 0.989 A0JPN4 →
Q8K330 0.986 Q8K330 →
Q9Y5B0 0.986 Q9Y5B0 →
Q8VDP4 0.986 Q8VDP4 →
Q32LQ1 0.986 Q32LQ1 →
O14529 0.986 O14529 →
TERF2 Telomeric repeat-binding factor 2 0.985 landscape →
Q8VDG6 0.985 Q8VDG6 →
Q08DK9 0.985 Q08DK9 →
A1L3T7 0.985 A1L3T7 →
RRP1B Ribosomal RNA processing protein 1 homolog B 0.985 landscape →
Q6PDM1 0.985 Q6PDM1 →
B1H224 0.985 B1H224 →
Q9HB65 0.985 Q9HB65 →
O18805 0.985 O18805 →
MSL1 Male-specific lethal 1 homolog 0.985 landscape →
CECR2 Chromatin remodeling regulator CECR2 0.985 landscape →
Q8K3I4 0.984 Q8K3I4 →
A2A9T0 0.984 A2A9T0 →
Q8NCF5 0.984 Q8NCF5 →
Q6PCQ0 0.984 Q6PCQ0 →
Q6P1D7 0.984 Q6P1D7 →
Q58CQ0 0.984 Q58CQ0 →
Q8BHZ4 0.984 Q8BHZ4 →
Q5D1E8 0.984 Q5D1E8 →
Q9GLM3 0.984 Q9GLM3 →
O35144 0.984 O35144 →
Q3TES0 0.984 Q3TES0 →
O09130 0.984 O09130 →