EPB41

Protein 4.1 · P11171 · EPB41 on Sugi Atlas →

0 patent compounds predicted against EPB41, 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 EPB41 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
Treatment of Ectopic Calcification in Fahr's Disease or Syndrome PHASE2RECRUITING
Peptide Vaccinations to Treat Patients With Low-Risk Myeloid Cancers PHASE2COMPLETED
Hemolysis in Patients With Hereditary Spherocytosis (HS) nanUNKNOWN
Human Epididymis Protein 4 in Endometrial Carcinoma nanCOMPLETED
PGE2/IL-22 Pathway in Various Forms of Eczema nanCOMPLETED
Characterization of New Candidate Genes in Cases of Human Inherited Thrombocytopenia (CATCH) nanCOMPLETED
Clinical and Genetic Analysis of Enlarged Vestibular Aqueducts nanCOMPLETED
Genotype-phenotype Correlation in Junctional Epidermolysis Bullosa nanUNKNOWN
Identifying Genes and Mutations Underlying Retinitis Pigmentosa and Allied Diseases nanUNKNOWN
Exploring the Genetics of Neuropathic Pain nanRECRUITING
Biomarker for Sanfilippo Type A-B-C-D Disease (BioSanfilippo) nanWITHDRAWN
Genetic Analysis of Heart Channelopathies in Brazilian Patients and Their Relatives nanUNKNOWN
Chromosome 5Q Gene Variants and Asthma-Related Traits nanCOMPLETED
Study of Constitutional Platelet Disease nanUNKNOWN
Muscle Tissue Bank for Muscular Dystrophy nanCOMPLETED
Hereditary Spastic Paraplegia Genomic Sequencing Initiative (HSPseq) nanRECRUITING
Impact of Elastin Mediated Vascular Stiffness on End Organs nanCOMPLETED
Nature and Frequency of Genetic Abnormalities and Associated Phenotypes in a Cohort of Adults With Intellectual Disability nanNOT_YET_RECRUITING
CP-EDIT: Cerebral Palsy - Early Diagnosis and Intervention Trial nanRECRUITING
Signs and Symptoms of Genetic Abnormalities Linked to Inherited Heart Disease nanCOMPLETED
Cross-sectional Characterization of Idiopathic Bronchiectasis nanCOMPLETED
The Association Between Post-ERCP Acute Pancreatitis and Various Genetic Mutations nanCOMPLETED
Signs and Symptoms Associated With Molecular Defects in Genetically Inherited Heart Disease nanCOMPLETED
Delineating the Molecular Spectrum and the Clinical, Imaging and Neuronal Phenotype of Chopra-Amiel-Gordon Syndrome nanRECRUITING
Epilepsy Phenome/Genome Project nanCOMPLETED
Characterization of WAGR Syndrome and Other Chromosome 11 Gene Deletions nanCOMPLETED
Young Pectus Excavatum Patients and Genetic Defects nanCOMPLETED
Update in VWD Laboratory Diagnosis nanUNKNOWN
Comparison of Two Methods to Diagnose Coronary Artery Disease nanCOMPLETED

Related proteins — ESM-2 sequence neighbours (a EPB41 binder may also engage these)

ProteinNameSimilarity
P48193 1.000 P48193 →
Q6Q7P4 1.000 Q6Q7P4 →
P11434 1.000 P11434 →
Q9WV92 1.000 Q9WV92 →
Q9H4G0 1.000 Q9H4G0 →
Q9WTP0 1.000 Q9WTP0 →
Q9Z2H5 0.999 Q9Z2H5 →
Q9Y2J2 0.999 Q9Y2J2 →
Q9N179 0.998 Q9N179 →
EPB41L2 Band 4.1-like protein 2 0.997 landscape →
A6QP06 0.997 A6QP06 →
Q9H329 0.996 Q9H329 →
O70318 0.996 O70318 →
Q99PI5 0.995 Q99PI5 →
Q8BGS1 0.995 Q8BGS1 →
O75167 0.994 O75167 →
Q17353 0.994 Q17353 →
Q28Z18 0.994 Q28Z18 →
BPTF Nucleosome-remodeling factor subunit BPTF 0.993 landscape →
Q1LYM3 0.993 Q1LYM3 →
A8KBE0 0.993 A8KBE0 →
Q8NDI1 0.993 Q8NDI1 →
O43150 0.993 O43150 →
Q5FVG2 0.993 Q5FVG2 →
Q9HCH5 0.993 Q9HCH5 →
A0JMK9 0.993 A0JMK9 →
Q22744 0.993 Q22744 →
Q05D44 0.993 Q05D44 →
Q5RAU1 0.993 Q5RAU1 →
Q06546 0.993 Q06546 →