EPB41L2

Band 4.1-like protein 2 · O43491 · EPB41L2 on Sugi Atlas →

0 patent compounds predicted against EPB41L2, 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 EPB41L2 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
Effects of an Intensified Treatment With ACE-I,ATA II and Statins in Alport Syndrome PHASE2COMPLETED
Melpida: Recombinant Adeno-associated Virus (serotype 9) Encoding a Codon Optimized Human AP4M1 Transgene (hAP4M1opt) PHASE1/PHASE2RECRUITING
Hemolysis in Patients With Hereditary Spherocytosis (HS) nanUNKNOWN
Epidemiological and Genetic Studies of Body Mass Index nanCOMPLETED
Chromosome 5Q Gene Variants and Asthma-Related Traits nanCOMPLETED
Genetics and Psychopathology in the 22q11 Deletion Syndrome nanUNKNOWN
Muscle Tissue Bank for Muscular Dystrophy nanCOMPLETED
Genetic Analysis of Heart Channelopathies in Brazilian Patients and Their Relatives nanUNKNOWN
Update in VWD Laboratory Diagnosis nanUNKNOWN
Genotype-phenotype Correlation in Junctional Epidermolysis Bullosa nanUNKNOWN
Hereditary Spastic Paraplegia Genomic Sequencing Initiative (HSPseq) nanRECRUITING
Characterization of New Candidate Genes in Cases of Human Inherited Thrombocytopenia (CATCH) nanCOMPLETED
Clinical and Genetic Analysis of Enlarged Vestibular Aqueducts nanCOMPLETED
Biomarker for Sanfilippo Type A-B-C-D Disease (BioSanfilippo) nanWITHDRAWN
Identifying Genes and Mutations Underlying Retinitis Pigmentosa and Allied Diseases nanUNKNOWN
Molecular Genetic Epidemiology of Endocardial Cushion Defects - SCOR in Pediatric Cardiovascular Disease nanCOMPLETED
PCM1-JAK2 in Therapy Related Neoplasms nanUNKNOWN
Exploring the Genetics of Neuropathic Pain nanRECRUITING
Mapping Novel Disease Genes for Dilated Cardiomyopathy nanCOMPLETED
A Study of the Interaction Between Tumor Susceptibility Gene Glycine N-methyltransferase (GNMT) and Lung Cancer nanUNKNOWN
Genetic Study of Familial Epilepsy nanCOMPLETED
Defining an Obesity QTL on Chromosome 3q nanCOMPLETED
Diet Intervention and GEnetic STudy (DIGEST-Pilot) nanUNKNOWN
Delineating the Molecular Spectrum and the Clinical, Imaging and Neuronal Phenotype of Chopra-Amiel-Gordon Syndrome nanRECRUITING
Genetic Studies of Inflammatory Bowel Disease nanCOMPLETED
Efficacy of Cognitive Rehabilitation Using Virtual Reality and Computer-based Cognitive Stimulation on Cognitive Impairment Associated to Movement Disorders nanCOMPLETED
A Positional Cloning Study on Schizophrenia nanCOMPLETED
Markers and Mechanisms of Macrovascular Disease in IDDM nanCOMPLETED
Natural History and Genetic Studies of Usher Syndrome nanCOMPLETED

Related proteins — ESM-2 sequence neighbours (a EPB41L2 binder may also engage these)

ProteinNameSimilarity
P48193 1.000 P48193 →
EPB41 Protein 4.1 1.000 landscape →
Q6Q7P4 1.000 Q6Q7P4 →
Q9WV92 1.000 Q9WV92 →
O70318 1.000 O70318 →
Q9WTP0 0.998 Q9WTP0 →
Q9Y2J2 0.998 Q9Y2J2 →
Q9H4G0 0.998 Q9H4G0 →
Q9Z2H5 0.998 Q9Z2H5 →
P11434 0.997 P11434 →
Q9H329 0.995 Q9H329 →
A6QP06 0.995 A6QP06 →
F1QIC4 0.994 F1QIC4 →
Q92539 0.994 Q92539 →
Q96B97 0.994 Q96B97 →
O75167 0.993 O75167 →
Q99PI5 0.993 Q99PI5 →
Q8IZ21 0.993 Q8IZ21 →
BPTF Nucleosome-remodeling factor subunit BPTF 0.993 landscape →
Q9N179 0.992 Q9N179 →
Q5RAU1 0.992 Q5RAU1 →
O60237 0.992 O60237 →
Q2PFD7 0.992 Q2PFD7 →
Q17353 0.992 Q17353 →
Q9FHY8 0.992 Q9FHY8 →
Q9HCH5 0.991 Q9HCH5 →
Q8NDI1 0.991 Q8NDI1 →
A2AD83 0.991 A2AD83 →
A2AHC3 0.991 A2AHC3 →
Q6NN85 0.991 Q6NN85 →