SLC25A4

ADP/ATP translocase 1 · P12235 · SLC25A4 on Sugi Atlas →

0 patent compounds predicted against SLC25A4, 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 SLC25A4 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Applying Proton Pump Inhibitor to Prevent and Treat Acute Fluctuating Hearing Loss in Patients With SLC26A4 Mutation PHASE2/PHASE3UNKNOWN
A Study of the Efficacy and Safety of MT1621 in Thymidine Kinase 2 (TK2) Deficiency (Treatment naïve) PHASE3WITHDRAWN
Phase III Trial of Coenzyme Q10 in Mitochondrial Disease PHASE3COMPLETED
Mitochondrial Dysfunction in the Pathophysiology and Treatment of Bipolar Disorder PHASE2WITHDRAWN
Natural History Study of SLC25A46 Mutation-related Mitochondriopathy nanCOMPLETED
Expression of SLC25A48 in Chronic Obstructive Pulmonary Disease nanNOT_YET_RECRUITING
Tissue Sample Study for Mitochondrial Disorders nanENROLLING_BY_INVITATION
Clinical and Genetic Analysis of Enlarged Vestibular Aqueducts nanCOMPLETED
Gastrointestinal Dysfunction in Children Affected With Mitochondrial Disorders nanCOMPLETED
GDF-15 as a Biomarker for Mitochondrial Disease nanCOMPLETED
Identification of New Candidate Genes in Patients With Mitochondrial Disease by High Resolution Chromosome Analysis on DNA Chip nanCOMPLETED
Human Mitochondrial Stress-driven Obesity Resistance nanCOMPLETED
Universal Rare Gene Study: A Registry and Natural History Study of Retinal Dystrophies Associated With Rare Disease-Causing Genetic Variants nanRECRUITING
The Natural History of Mitochondrial Diseases nanRECRUITING
Genetic and Biohumoral Factors Involved in Menière's Disease and Their Correlation With Phenotypes nanRECRUITING
Natural History Study of ATP1A3-related Disease nanUNKNOWN
A Study Into the Underlying Biochemical Pathways Involved in Parkinson's Disease, Such as Mitochondrial (Cellular Powerhouse) Dysfunction nanCOMPLETED
Exercise-mediated Rescue of Mitochondrial Dysfunctions Driving Insulin Resistance nanCOMPLETED
Multi-omics Study in Citrin Deficiency nanACTIVE_NOT_RECRUITING
A Retrospective Survey-based Multicenter Study to Delineate the Molecular and Phenotypic Spectrum of Epilepsy-dyskinesia Syndromes nanRECRUITING
Calf Muscle Strength in Mitochondrial Diseases nanCOMPLETED
Genetic Variations That Increase the Risk for Calcium Kidney Stones: a Family-based Study nanCOMPLETED
MITOMICS : a Multi-OMICS Approach for the Diagnosis of Mitochondrial Diseases nanRECRUITING
North American Mitochondrial Disease Consortium Patient Registry and Biorepository (NAMDC) nanRECRUITING
Identification and Characterization of Monogenic Diabetes nanCOMPLETED
Mitochondrial Dysfunction in Phelan-McDermid Syndrome nanCOMPLETED
Mitochondrial Dysfunctions Driving Insulin Resistance nanCOMPLETED
Mitoquines in COPD nanUNKNOWN
Pathogenic Insights and Search for Biomarkers in RFC1-ataxia/CANVAS nanRECRUITING
Oxalate and Citrate in Humans - Response to Citrate nanRECRUITING

Related proteins — ESM-2 sequence neighbours (a SLC25A4 binder may also engage these)

ProteinNameSimilarity
P02722 1.000 P02722 →
Q6QRN9 1.000 Q6QRN9 →
Q5R5A1 1.000 Q5R5A1 →
P32007 1.000 P32007 →
Q000K2 1.000 Q000K2 →
SLC25A6 ADP/ATP translocase 3 1.000 landscape →
Q05962 1.000 Q05962 →
P48962 1.000 P48962 →
SLC25A5 ADP/ATP translocase 2 1.000 landscape →
Q8SQH5 1.000 Q8SQH5 →
P51881 1.000 P51881 →
O46373 0.997 O46373 →
Q09073 0.991 Q09073 →
Q7PQV7 0.968 Q7PQV7 →
Q27238 0.967 Q27238 →
F1R4U0 0.960 F1R4U0 →
Q26365 0.957 Q26365 →
P97700 0.950 P97700 →
SLC25A11 Mitochondrial 2-oxoglutarate/malate carrier protein 0.947 landscape →
Q8HXY2 0.946 Q8HXY2 →
P32089 0.942 P32089 →
SLC25A20 Mitochondrial carnitine/acylcarnitine carrier protein 0.942 landscape →
P79110 0.941 P79110 →
SLC25A1 Tricarboxylate transport protein, mitochondrial 0.941 landscape →
O97649 0.940 O97649 →
Q9Z2Z6 0.940 Q9Z2Z6 →
P55851 0.939 P55851 →
Q5R5A8 0.939 Q5R5A8 →
Q3SZI5 0.939 Q3SZI5 →
Q8JZU2 0.938 Q8JZU2 →