ABCB7

Iron-sulfur clusters transporter ABCB7, mitochondrial · O75027 · ABCB7 on Sugi Atlas →

0 patent compounds predicted against ABCB7, 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 ABCB7 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Bovine Lactoferrin to Prevent and Cure Iron Deficiency and Iron Deficiency Anemia in Complicated Pregnancies PHASE4COMPLETED
Effect of Pioglitazone Administered to Patients With Friedreich's Ataxia: Proof of Concept PHASE3COMPLETED
Testing the Combination of MLN4924 (Pevonedistat), Carboplatin, and Paclitaxel in Patients With Advanced Non-small Cell Lung Cancer (NSCLC) Who Have Previously Been Treated With Immunotherapy PHASE2ACTIVE_NOT_RECRUITING
Atorvastatin, L-Carnitine and Non-Alcoholic Steatohepatitis PHASE2UNKNOWN
A Study of Bezafibrate in Mitochondrial Myopathy PHASE2COMPLETED
Natural History Study of FDXR Mutation-related Mitochondriopathy nanCOMPLETED
Tissue Sample Study for Mitochondrial Disorders nanENROLLING_BY_INVITATION
Mitoferrin-1 Expression in Erythropoietic Protoporphyria (Porphyria Rare Disease Clinical Research Consortium (RDCRC)) nanCOMPLETED
FRIEDREICH ATAXIA- STEROIDOGENESIS nanCOMPLETED
Polycystic Ovary Syndrome in Type 1 Diabetes nanNOT_YET_RECRUITING
Investigations Into ISCU Myopathy or Iron Sulfur Scaffold U Protein Myopathy nanCOMPLETED
Iron Overload in African Americans nanCOMPLETED
Multidrug Resistance Genes in Patients With Acute Myeloid Leukemia nanACTIVE_NOT_RECRUITING
Relationship of Haptoglobin Phenotype to Vascular Function and Response to Vitamin E Supplementation in Patients With Diabetes Mellitus Type 2: The EVAS Trial nanUNKNOWN
Phenotypic and Genotypic Studies in Congenital and Early Onset Ataxias nanCOMPLETED
Biocollection in MyeloDysplastic Syndrome (P-MDS) nanRECRUITING
Identification of New Candidate Genes in Patients With Mitochondrial Disease by High Resolution Chromosome Analysis on DNA Chip nanCOMPLETED
Role of the ATP7A Transporter in Ovarian Cancer nanCOMPLETED
Genetic Regulation of Surfactant Deficiency nanCOMPLETED
Clinical Study of Hydroxytyrosol (HT) in Mitochondrial Diseases nanCOMPLETED
Effect of Subtle Energy Transmission and Tao Calligraphy Mindfulness Practice on Mitochondrial DNA in Peripheral Blood Leukocytes nanNOT_YET_RECRUITING
Genetic Causes and Clinical Features of Childhood Interstitial Lung Diseases in China nanCOMPLETED
The Natural History of Mitochondrial Diseases nanRECRUITING
A Feasibility Study: Assessing Photobiomodulation in Myalgic Encephalomyelitis nanUNKNOWN
Hemochromatosis and Iron Overload Screening Study (HEIRS) nanCOMPLETED
Utilizing Non-Invasive Fibroscan® Technology to Identify Genetic Markers for Fatty Liver Progression nanCOMPLETED
Genomic of CONgenital Sideroblastic Anemias nanRECRUITING
Coproporphyrine Isomers and Methotrexate Elimination nanCOMPLETED
Validation of a Prognostic Biomarker Using Brain Diffusion MRI in X-linked Adrenoleukodystrophy nanNOT_YET_RECRUITING
Establishment of Human Cellular Disease Models for Wilson Disease nanCOMPLETED

Related proteins — ESM-2 sequence neighbours (a ABCB7 binder may also engage these)

ProteinNameSimilarity
Q704E8 1.000 Q704E8 →
E7F6F7 0.995 E7F6F7 →
Q751N2 0.995 Q751N2 →
H2LNR5 0.995 H2LNR5 →
Q61102 0.994 Q61102 →
J9VWU3 0.994 J9VWU3 →
P0CL93 0.993 P0CL93 →
P0CL92 0.993 P0CL92 →
O14286 0.992 O14286 →
Q5B1Q2 0.992 Q5B1Q2 →
Q4WLN7 0.992 Q4WLN7 →
Q4PH16 0.990 Q4PH16 →
Q7RX59 0.990 Q7RX59 →
Q6CX96 0.990 Q6CX96 →
Q9LVM1 0.989 Q9LVM1 →
Q6FIK3 0.989 Q6FIK3 →
P40416 0.988 P40416 →
Q2ULH4 0.988 Q2ULH4 →
Q4HVU7 0.987 Q4HVU7 →
Q9M0G9 0.986 Q9M0G9 →
Q6C6N0 0.986 Q6C6N0 →
Q6BXD7 0.985 Q6BXD7 →
Q9JJ59 0.983 Q9JJ59 →
Q56A55 0.982 Q56A55 →
Q9FUT3 0.979 Q9FUT3 →
Q8T9W2 0.979 Q8T9W2 →
Q08D64 0.978 Q08D64 →
Q9QYJ4 0.978 Q9QYJ4 →
Q9Y7M7 0.977 Q9Y7M7 →
Q9CXJ4 0.977 Q9CXJ4 →