VPS26B

Vacuolar protein sorting-associated protein 26B · Q4G0F5 · VPS26B on Sugi Atlas →

0 patent compounds predicted against VPS26B, 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 VPS26B by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Safety and Efficacy of AAV9/AP4B1 (BFB-101) For Patients With AP4B1-related Hereditary Spastic Paraplegia Type 47 (SPG47) PHASE1/PHASE2NOT_YET_RECRUITING
Melpida: Recombinant Adeno-associated Virus (serotype 9) Encoding a Codon Optimized Human AP4M1 Transgene (hAP4M1opt) PHASE1/PHASE2RECRUITING
Study of IV VTS-270 for Infantile Liver Disease Associated With Niemann-Pick Disease, Type C PHASE1/PHASE2COMPLETED
Reverse Transcriptase Inhibitors in AGS PHASE2COMPLETED
Nilotinib in Huntington's Disease PHASE1UNKNOWN
Natural History Study of SLC25A46 Mutation-related Mitochondriopathy nanCOMPLETED
Clinical and Genetic Analysis of Enlarged Vestibular Aqueducts nanCOMPLETED
Autophagy in Systemic Lupus Erythematosus nanUNKNOWN
Assessing the Polygenic Burden of Rare Disruptive Mutations in Parkinson's Disease nanUNKNOWN
Natural History Study of Patients With VCP-related Disease nanCOMPLETED
Study of Chediak-Higashi Syndrome nanRECRUITING
Genetic Characterization of Parkinson's Disease nanCOMPLETED
Genetic Studies of Lysosomal Storage Disorders nanENROLLING_BY_INVITATION
Identifying Genes and Mutations Underlying Retinitis Pigmentosa and Allied Diseases nanUNKNOWN
The Natural History of Alpha-Mannosidosis nanCOMPLETED
Classification, Functional Stratification and Biomarkers in Ciliopathy (CILLICORIRCM) nanCOMPLETED
Registry and Natural History of Epilepsy-Dyskinesia Syndromes nanRECRUITING
Biomarker Research in Inherited Movement Disorders nanRECRUITING
Study of Usher Syndromes, Type 1 and Type 2 nanCOMPLETED
Genetic Analysis of Hereditary Disorders of Hearing and Balance nanCOMPLETED
Evaluation of Serum Gasdermin D Level As a Potential Biomarker of Disease Activity in Vitiligo Patients nanUNKNOWN
PET/CT Scans Using the Tracer 11C-Csar, a Bile Acid Analog, to Depict and Visualize Changes in the Hepatobiliary System in Patients With Primary Biliary Cholangitis Before and After Treatment. nanACTIVE_NOT_RECRUITING
Study of Neurodegenerative Diseases Induced Stem Cells in Patients and Healthy Family Controls. nanUNKNOWN
Genetic Analysis of Fraser Syndrome and Fryns Syndrome nanCOMPLETED
Diagnosis of Primary Ciliary Dyskinesia nanCOMPLETED
Registry Gangliosidoses nanUNKNOWN
Association of Autophagy-related Genes ,LncRNA and SNPs With Colorectal Cancer in Egyptian Population nanCOMPLETED
Nuclear Myosin VI - a Therapeutic Target in Breast Cancer nanUNKNOWN
Markers and Mechanisms of Macrovascular Disease in IDDM nanCOMPLETED
Genetic Investigations in Children With Developmental and Epileptic Encephalopathies in Ho Chi Minh City, Vietnam nanUNKNOWN

Related proteins — ESM-2 sequence neighbours (a VPS26B binder may also engage these)

ProteinNameSimilarity
Q5R436 1.000 Q5R436 →
Q5BKM4 1.000 Q5BKM4 →
Q8C0E2 1.000 Q8C0E2 →
Q6DFB9 1.000 Q6DFB9 →
Q6IRD0 1.000 Q6IRD0 →
Q68F29 1.000 Q68F29 →
Q9T091 1.000 Q9T091 →
Q10243 1.000 Q10243 →
O01258 1.000 O01258 →
Q7ZV03 1.000 Q7ZV03 →
Q6DH23 1.000 Q6DH23 →
Q0VD53 1.000 Q0VD53 →
P40336 1.000 P40336 →
Q6TNP8 1.000 Q6TNP8 →
Q28HT6 1.000 Q28HT6 →
Q9FJD0 1.000 Q9FJD0 →
Q6AY86 1.000 Q6AY86 →
VPS26A Vacuolar protein sorting-associated protein 26A 1.000 landscape →
Q6DFU4 0.999 Q6DFU4 →
Q55CA0 0.995 Q55CA0 →
Q9W552 0.992 Q9W552 →
Q8I4T1 0.990 Q8I4T1 →
P40335 0.987 P40335 →
Q19829 0.986 Q19829 →
C5DL84 0.986 C5DL84 →
Q9USS1 0.986 Q9USS1 →
C5DRZ0 0.986 C5DRZ0 →
Q6CTM7 0.985 Q6CTM7 →
Q10347 0.984 Q10347 →
G5EFD2 0.983 G5EFD2 →