GOLT1B

Vesicle transport protein GOT1B · Q9Y3E0 · GOLT1B on Sugi Atlas →

0 patent compounds predicted against GOLT1B, 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 GOLT1B 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
Safety and Efficacy of AAV9/AP4B1 (BFB-101) For Patients With AP4B1-related Hereditary Spastic Paraplegia Type 47 (SPG47) PHASE1/PHASE2NOT_YET_RECRUITING
Acute Effect of HP-211 (Axulin) on Blood Glucose and Serum Insulin Responses in Healthy Lean and Overweight Humans PHASE1COMPLETED
Study of Chediak-Higashi Syndrome nanRECRUITING
Genetic Variation in CLTCL1 and Whole-body Glucose Control nanCOMPLETED
Genetic Investigations in Children With Developmental and Epileptic Encephalopathies in Ho Chi Minh City, Vietnam nanUNKNOWN
Hepatic Substrate Flux Rates in Type 2 Diabetes nanACTIVE_NOT_RECRUITING
Genetic Analysis of Gray Platelet Syndrome nanCOMPLETED
High Fat Diet for Cardiac Metabolic Reprogramming nanRECRUITING
Gait in Rare Diseases nanCOMPLETED
Genetic Studies of Lysosomal Storage Disorders nanENROLLING_BY_INVITATION
The Classification and Cause of Leukodystrophies of Unknown Cause nanCOMPLETED
Role of the Liver in Glucose Homeostasis Using Metabolic Imaging nanCOMPLETED
Fatty Acid Metabolism and Insulin Sensitivity: the Role of Endurance Exercise nanCOMPLETED
Genetic Characterization of Parkinson's Disease nanCOMPLETED
The LD Lync Study - Natural History Study of Lipodystrophy Syndromes nanRECRUITING
A Patient-tailored Genetic/Biomarker/iPSC Combined Approach in ALS - PERMEALS nanRECRUITING
Registry Gangliosidoses nanUNKNOWN
Genetic and Metabolic Disease in Children nanRECRUITING
Establishment of Human Cellular Disease Models for Wilson Disease nanCOMPLETED
The Natural History of Alpha-Mannosidosis nanCOMPLETED
Molecular Analysis of Patients With Neuromuscular Disease nanRECRUITING
Registry and Natural History of Epilepsy-Dyskinesia Syndromes nanRECRUITING
Identification and Characterization of Monogenic Diabetes nanCOMPLETED
Identification of New Biomarkers of Insulin Resistance nanACTIVE_NOT_RECRUITING
Induced Pluripotent Stem Cells for Niemann Pick Disease nanCOMPLETED
Mapping Novel Disease Genes for Dilated Cardiomyopathy nanCOMPLETED
Natural History Study of SLC25A46 Mutation-related Mitochondriopathy nanCOMPLETED
Sexually Dimorphic Effects of GHRH in Adult Growth Hormone Testing nanCOMPLETED
Glycosylation in Patients With Galactosaemia nanCOMPLETED

Related proteins — ESM-2 sequence neighbours (a GOLT1B binder may also engage these)

ProteinNameSimilarity
Q2YDE3 1.000 Q2YDE3 →
Q9CR60 1.000 Q9CR60 →
Q2NKV8 0.999 Q2NKV8 →
Q20263 0.998 Q20263 →
Q6ZVE7 0.998 Q6ZVE7 →
Q03554 0.994 Q03554 →
Q6NMM1 0.994 Q6NMM1 →
Q9DCQ3 0.992 Q9DCQ3 →
Q9USJ2 0.992 Q9USJ2 →
Q54CL4 0.990 Q54CL4 →
O14223 0.973 O14223 →
Q4FZV2 0.973 Q4FZV2 →
A3LPS1 0.972 A3LPS1 →
O74375 0.971 O74375 →
Q8WV19 0.970 Q8WV19 →
Q95T12 0.969 Q95T12 →
Q5SSN7 0.969 Q5SSN7 →
Q6CC06 0.969 Q6CC06 →
Q6FN38 0.968 Q6FN38 →
A5DEQ7 0.968 A5DEQ7 →
B2AR67 0.968 B2AR67 →
B4L0H1 0.967 B4L0H1 →
Q5U3Y5 0.967 Q5U3Y5 →
Q9P6K1 0.967 Q9P6K1 →
Q6BWE7 0.967 Q6BWE7 →
Q8VD57 0.967 Q8VD57 →
Q86I95 0.967 Q86I95 →
A7S4N4 0.967 A7S4N4 →
A7TS55 0.967 A7TS55 →
B4LIH0 0.966 B4LIH0 →