ORMDL3

ORM1-like protein 3 · Q8N138 · ORMDL3 on Sugi Atlas →

0 patent compounds predicted against ORMDL3, 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 ORMDL3 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Safety and Tolerability of Subretinally Injected OPGx-BEST1 in Patients With Best Vitelliform Macular Dystrophy (BVMD) or Autosomal-Recessive Bestrophinopathy (ARB) PHASE1/PHASE2RECRUITING
New Strategies of Genetic Study of Patients With Oculocutaneous Albinism nanCOMPLETED
Evaluation of Limb-Girdle Muscular Dystrophy nanCOMPLETED
Muscle Tissue Bank for Muscular Dystrophy nanCOMPLETED
The Role of CGRPand Nociceptin in Migraine nanUNKNOWN
Identification of an Asthma Susceptibility Gene on 3P nanCOMPLETED
The Influence of Genetic Variations in ELAPOR1 or ELAPOR2 on Insulin Secretion and Glucose Regulation in Humans nanUNKNOWN
Mapping Novel Disease Genes for Dilated Cardiomyopathy nanCOMPLETED
Molecular Analysis of Patients With Neuromuscular Disease nanRECRUITING
Genetic Characterization of Parkinson's Disease nanCOMPLETED
Genetics of Cardiovascular and Neuromuscular Disease nanRECRUITING
A Multicenter Phenotype-Genotype Analysis of LGMD Patients in China nanENROLLING_BY_INVITATION
Genetics of Primary Ciliary Dyskinesia nanCOMPLETED
Stress and Treatment Response in Puerto Rican Children With Asthma nanCOMPLETED
Protein Expression as a Potential Diagnostic Biomarker of Cervical Dysplasia and/or Cancer nanCOMPLETED
Study of the Pathophysiological Mechanisms Involved in Bleeding Events nanCOMPLETED
Characterization of New Candidate Genes in Cases of Human Inherited Thrombocytopenia (CATCH) nanCOMPLETED
CoMPaSS-NMD - Computational Models for New Patients Stratification Strategies of HNMD nanENROLLING_BY_INVITATION
Genetic Basis of Non Syndromic Congenital Diaphragmatic Hernia nanCOMPLETED
The LD Lync Study - Natural History Study of Lipodystrophy Syndromes nanRECRUITING
Predisposition Genes in Monogenic Diabetes (DIAMONO) nanCOMPLETED
Changes of Motor Function Tests in Congenital Myopathy Subjects Treated With Oral Salbutamol as Compared to no Treatment nanCOMPLETED
Prevalence of a Non-Expressing 11B Mutation in Aka Peoples of the Central African Republic nanCOMPLETED
Myotubular Myopathy Genetic Testing Study nanCOMPLETED
Genetic Analysis of Hereditary Disorders of Hearing and Balance nanCOMPLETED
The Collaborative Longitudinal Evaluation of Ethnicity and Refractive Error (CLEERE) Study nanUNKNOWN
Genetic Expression Alteration Affect on Lateral Neck Node Metastasis of Thyroid Papillary Microcarcinoma : Microarray Analysis nanCOMPLETED
Classification, Functional Stratification and Biomarkers in Ciliopathy (CILLICORIRCM) nanCOMPLETED
Natural History Study of Oculopharyngeal Muscular Dystrophy nanWITHDRAWN
Transcranial Magnetic Stimulation (TMS) Studies of Dystonia nanCOMPLETED

Related proteins — ESM-2 sequence neighbours (a ORMDL3 binder may also engage these)

ProteinNameSimilarity
Q0VD15 1.000 Q0VD15 →
Q5XJR6 1.000 Q5XJR6 →
Q9CQZ0 1.000 Q9CQZ0 →
Q8JFB7 1.000 Q8JFB7 →
Q9CPZ6 1.000 Q9CPZ6 →
Q5R570 1.000 Q5R570 →
Q5ZIU0 1.000 Q5ZIU0 →
D2I2F3 1.000 D2I2F3 →
Q9P0S3 1.000 Q9P0S3 →
Q5R8X5 1.000 Q5R8X5 →
Q5E972 1.000 Q5E972 →
Q921I0 1.000 Q921I0 →
Q29RQ9 1.000 Q29RQ9 →
Q5XH57 1.000 Q5XH57 →
Q6QI25 1.000 Q6QI25 →
Q96495 1.000 Q96495 →
O42901 1.000 O42901 →
Q53FV1 1.000 Q53FV1 →
Q9VP04 0.997 Q9VP04 →
P53224 0.995 P53224 →
Q9Y7R5 0.993 Q9Y7R5 →
Q06144 0.993 Q06144 →
Q8TFH6 0.992 Q8TFH6 →
Q3T0S0 0.991 Q3T0S0 →
Q9Y876 0.991 Q9Y876 →
Q55GT5 0.990 Q55GT5 →
C4Y206 0.990 C4Y206 →
Q6FSD1 0.989 Q6FSD1 →
Q9CZB9 0.989 Q9CZB9 →
Q9P7C2 0.989 Q9P7C2 →