FAM162A

Protein FAM162A · Q96A26 · FAM162A on Sugi Atlas →

0 patent compounds predicted against FAM162A, 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 FAM162A by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Treatment of Ectopic Calcification in Fahr's Disease or Syndrome PHASE2RECRUITING
Folate Receptor Alpha Peptide Vaccine With GM-CSF in Patients With Triple Negative Breast Cancer PHASE2COMPLETED
Expression of Fas Protein in Skin Biopsies of Participants With Scarring Alopecia nanCOMPLETED
Transcranial Magnetic Stimulation (TMS) Studies of Dystonia nanCOMPLETED
Genetic Characterization of Parkinson's Disease nanCOMPLETED
Molecular Genetic Epidemiology of Endocardial Cushion Defects - SCOR in Pediatric Cardiovascular Disease nanCOMPLETED
Identification of New FTLD Genes nanUNKNOWN
Characterization of New Candidate Genes in Cases of Human Inherited Thrombocytopenia (CATCH) nanCOMPLETED
Autophagy Bladder Cancer nanUNKNOWN
Role of Sorcin and Annexin A3 in Breast Cancer Patients nanUNKNOWN
Protein Expression as a Potential Diagnostic Biomarker of Cervical Dysplasia and/or Cancer nanCOMPLETED
Familial Partial Lipodystrophy Study nanCOMPLETED
Mapping Novel Disease Genes for Dilated Cardiomyopathy nanCOMPLETED
Clinical and Genetic Studies of Familial Presenile Dementia With Neuronal Inclusion Bodies nanCOMPLETED
Muscle Tissue Bank for Muscular Dystrophy nanCOMPLETED
Genetic Markers for Focal Segmental Glomerulosclerosis nanCOMPLETED
Identification of Genetic Variants Associated With Unexpected Infant Death Syndrome nanRECRUITING
Genetic Basis of Non Syndromic Congenital Diaphragmatic Hernia nanCOMPLETED
Prevalence of a Non-Expressing 11B Mutation in Aka Peoples of the Central African Republic nanCOMPLETED
Genetic Determinant of Foveolar Hypoplasia in Parents of Albinos Children nanCOMPLETED
Human Epilepsy Genetics--Neuronal Migration Disorders Study nanRECRUITING
New Genes Involved in Molecular Etiology of Rett Syndrome Through DNA Microarray Comparative Genomic Hybridization nanCOMPLETED
Genetic Analysis of Fraser Syndrome and Fryns Syndrome nanCOMPLETED
The Influence of Genetic Variations in ELAPOR1 or ELAPOR2 on Insulin Secretion and Glucose Regulation in Humans nanUNKNOWN
Identification of an Asthma Susceptibility Gene on 3P nanCOMPLETED
Exome Analysis in Hearing Impaired Patients nanUNKNOWN
Genetics of Endocrine Tumours - Familial Isolated Pituitary Adenoma - FIPA nanRECRUITING
Validation of a Clinical Algorithm for the Diagnosis of Recessive Ataxias nanCOMPLETED
Pharmacogenomic Association Study in Indian Children With Acute Lymphoblastic Leukemia nanRECRUITING
FGL2/Fibroleukin and Hepatitis C Virus Infection: A Predictor of Response to Antiviral Therapy nanCOMPLETED

Related proteins — ESM-2 sequence neighbours (a FAM162A binder may also engage these)

ProteinNameSimilarity
Q5R504 1.000 Q5R504 →
Q9D6U8 1.000 Q9D6U8 →
Q4QQV3 1.000 Q4QQV3 →
Q2NKR7 0.999 Q2NKR7 →
A3KP48 0.991 A3KP48 →
Q5U2X7 0.987 Q5U2X7 →
Q9VW12 0.986 Q9VW12 →
Q863G0 0.985 Q863G0 →
O74988 0.985 O74988 →
A8WGU8 0.985 A8WGU8 →
Q9W549 0.984 Q9W549 →
A8KB87 0.983 A8KB87 →
Q0MQD7 0.983 Q0MQD7 →
Q7TNN2 0.983 Q7TNN2 →
Q9CQH3 0.983 Q9CQH3 →
Q02376 0.982 Q02376 →
Q02380 0.982 Q02380 →
Q4V7Q1 0.981 Q4V7Q1 →
Q290M9 0.981 Q290M9 →
Q0MQJ3 0.981 Q0MQJ3 →
Q3E870 0.981 Q3E870 →
Q7YRF4 0.981 Q7YRF4 →
Q863F9 0.981 Q863F9 →
Q80VP5 0.981 Q80VP5 →
Q8HXG5 0.981 Q8HXG5 →
Q9Y811 0.980 Q9Y811 →
Q8TF08 0.980 Q8TF08 →
Q9D8H7 0.980 Q9D8H7 →
P16221 0.980 P16221 →
Q0MQC7 0.980 Q0MQC7 →