TMEM126A

Transmembrane protein 126A · Q9H061 · TMEM126A on Sugi Atlas →

0 patent compounds predicted against TMEM126A, 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 TMEM126A by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Weight Loss Study: Genetics and Response to Naltrexone/Bupropion PHASE4RECRUITING
A Multicenter Study of NAP (AL-108) in Schizophrenia PHASE2COMPLETED
Role of TLR4 in Environmental Asthma PHASE1COMPLETED
Clinical and Genetic Analysis of Enlarged Vestibular Aqueducts nanCOMPLETED
Evaluation of CEMIP in Pancreatic Cancer nanUNKNOWN
Phenotypic and Genotypic Studies in Congenital and Early Onset Ataxias nanCOMPLETED
Natural History Study of SLC25A46 Mutation-related Mitochondriopathy nanCOMPLETED
Brain P-gp and Inflammation in People With Epilepsy nanCOMPLETED
Clinical Application of PET Imaging Targeting GPA33 in Malignant Tumors nanNOT_YET_RECRUITING
Chromosome 5Q Gene Variants and Asthma-Related Traits nanCOMPLETED
Characterization of New Candidate Genes in Cases of Human Inherited Thrombocytopenia (CATCH) nanCOMPLETED
Markers and Mechanisms of Macrovascular Disease in IDDM nanCOMPLETED
Exome Analysis in Hearing Impaired Patients nanUNKNOWN
Genetic Analyses of Nonsyndromic and Syndromic Deafness in Pakistan nanENROLLING_BY_INVITATION
PCD New Gene Discovery nanCOMPLETED
Genes, Proteins, and Metabolites in Drug-resistant Epilepsy (DRE) Patients nanNOT_YET_RECRUITING
Biomarker Research in Inherited Movement Disorders nanRECRUITING
Sj-subway, a Predictor for the Recurrence of High-risk Hormone Receptor-positive Breast That is Sensitive to Extended Endocrine Therapy nanRECRUITING
Study of Usher Syndromes, Type 1 and Type 2 nanCOMPLETED
Biomarkers of Lichen Sclerosus nanUNKNOWN
Studies on the Expression and Functions of RLIP76 in Blood Samples of Healthy Human Subjects nanWITHDRAWN
Genetic Mechanisms of Chronic Obstructive Pulmonary Disease (COPD) nanCOMPLETED
Clinical, Cellular, and Molecular Investigation Into Oculocutaneous Albinism nanCOMPLETED
Biomarkers of Risk of Parkinson Disease nanCOMPLETED
Whole Genome Scan of Extended Families With Familial Vocal Cord Paralysis nanCOMPLETED
A Family Study of Copy Number Variations in Patients With Autism Spectrum Disorder nanCOMPLETED
Identifying Genes and Mutations Underlying Retinitis Pigmentosa and Allied Diseases nanUNKNOWN
Genetic Basis of Non Syndromic Congenital Diaphragmatic Hernia nanCOMPLETED
New Strategies of Genetic Study of Patients With Oculocutaneous Albinism nanCOMPLETED
Genetic Characterization of Parkinson's Disease nanCOMPLETED

Related proteins — ESM-2 sequence neighbours (a TMEM126A binder may also engage these)

ProteinNameSimilarity
Q5RAY9 1.000 Q5RAY9 →
Q5HZA9 1.000 Q5HZA9 →
Q32L86 1.000 Q32L86 →
Q9D8Y1 0.998 Q9D8Y1 →
Q9VLM7 0.997 Q9VLM7 →
Q8IUX1 0.989 Q8IUX1 →
Q9D1R1 0.987 Q9D1R1 →
Q3T0M2 0.987 Q3T0M2 →
B2RZD2 0.986 B2RZD2 →
Q6P4A7 0.985 Q6P4A7 →
A8E7G5 0.984 A8E7G5 →
Q9VN13 0.981 Q9VN13 →
B6IJ52 0.980 B6IJ52 →
Q8T3C8 0.979 Q8T3C8 →
Q09201 0.979 Q09201 →
Q8IQ56 0.978 Q8IQ56 →
Q54NQ9 0.978 Q54NQ9 →
Q5FC79 0.978 Q5FC79 →
Q925N1 0.978 Q925N1 →
Q5RD16 0.977 Q5RD16 →
Q12029 0.977 Q12029 →
P87275 0.976 P87275 →
C8Z7B2 0.976 C8Z7B2 →
SFXN1 Sideroflexin-1 0.976 landscape →
Q6PBI8 0.976 Q6PBI8 →
Q9P055 0.976 Q9P055 →
Q28FG4 0.976 Q28FG4 →
C7GRS7 0.976 C7GRS7 →
SFXN3 Sideroflexin-3 0.976 landscape →
Q925N2 0.976 Q925N2 →