Sugi Predict

Sugi Predict / Targets / FAM222B

FAM222B

Protein FAM222B · Q8WU58 · FAM222B on Sugi Atlas →

0 patent compounds predicted against FAM222B, 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 FAM222B by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Treatment of Ectopic Calcification in Fahr's Disease or Syndrome PHASE2RECRUITING
FGL2/Fibroleukin and Hepatitis C Virus Infection: A Predictor of Response to Antiviral Therapy nanCOMPLETED
Genetic Characterization of Parkinson's Disease nanCOMPLETED
Molecular Genetic Epidemiology of Endocardial Cushion Defects - SCOR in Pediatric Cardiovascular Disease nanCOMPLETED
Identification of Genetic Variants Associated With Unexpected Infant Death Syndrome nanRECRUITING
Epidemiological and Genetic Studies of Body Mass Index nanCOMPLETED
Expression of Fas Protein in Skin Biopsies of Participants With Scarring Alopecia nanCOMPLETED
Genetic Determinants of Sudden Cardiac Death nanCOMPLETED
Studying Tissue Samples From Patients With Stage II Colon Cancer Treated on Clinical Trial CLB-9581 nanCOMPLETED
Characterization of New Candidate Genes in Cases of Human Inherited Thrombocytopenia (CATCH) nanCOMPLETED
Prevalence of a Non-Expressing 11B Mutation in Aka Peoples of the Central African Republic nanCOMPLETED
Transcranial Magnetic Stimulation (TMS) Studies of Dystonia nanCOMPLETED
FGL2/Fibroleukin and Hepatitis C Virus Recurrence Post Liver Transplantation nanUNKNOWN
Identification of an Asthma Susceptibility Gene on 3P nanCOMPLETED
Genetics of Recurrent Early Onset Major Depression nanCOMPLETED
Exome Analysis in Hearing Impaired Patients nanUNKNOWN
Genetic Study of Age-Related Macular Degeneration nanCOMPLETED
Markers and Mechanisms of Macrovascular Disease in IDDM nanCOMPLETED
Pharmacogenomic Association Study in Indian Children With Acute Lymphoblastic Leukemia nanRECRUITING
Genetic Markers for Focal Segmental Glomerulosclerosis nanCOMPLETED
Genetic Analysis of Familial Cases of Premature Ovarian Failure nanCOMPLETED
Genetic Markers of Coronary Heart Disease in Type 2 Diabetes nanCOMPLETED
New Genes Involved in Molecular Etiology of Rett Syndrome Through DNA Microarray Comparative Genomic Hybridization nanCOMPLETED
Genetics and Psychopathology in the 22q11 Deletion Syndrome nanUNKNOWN
Genetic Analysis of Fraser Syndrome and Fryns Syndrome nanCOMPLETED
Common Genetic Variation and Type 2 Diabetes nanCOMPLETED
Genetic Determinant of Foveolar Hypoplasia in Parents of Albinos Children nanCOMPLETED
Genetic Investigations in Children With Developmental and Epileptic Encephalopathies in Ho Chi Minh City, Vietnam nanUNKNOWN
Study on Moebius Syndrome and Congenital Facial Weakness Disorders nanCOMPLETED
Genetic Basis of Non Syndromic Congenital Diaphragmatic Hernia nanCOMPLETED

Related proteins — ESM-2 sequence neighbours (a FAM222B binder may also engage these)

ProteinNameSimilarity
Q6P539 — 0.999 Q6P539 →
Q5U5X8 — 0.996 Q5U5X8 →
Q6PGH4 — 0.994 Q6PGH4 →
Q66JW3 — 0.992 Q66JW3 →
Q3UHR0 — 0.992 Q3UHR0 →
O94900 — 0.992 O94900 →
Q9P267 — 0.991 Q9P267 →
Q1KKW8 — 0.990 Q1KKW8 →
A2D4R4 — 0.990 A2D4R4 →
P14653 — 0.990 P14653 →
Q6ZTU2 — 0.990 Q6ZTU2 →
Q9BDI3 — 0.990 Q9BDI3 →
P21999 — 0.989 P21999 →
P47806 — 0.989 P47806 →
Q96L91 — 0.989 Q96L91 →
A2T6H5 — 0.989 A2T6H5 →
GLI1 Zinc finger protein GLI1 0.989 landscape →
Q1KL10 — 0.989 Q1KL10 →
Q3V5Z9 — 0.989 Q3V5Z9 →
O89038 — 0.989 O89038 →
A2T7J2 — 0.988 A2T7J2 →
A1YG01 — 0.988 A1YG01 →
P08152 — 0.988 P08152 →
Q1KKX5 — 0.988 Q1KKX5 →
P48031 — 0.988 P48031 →
Q80WT2 — 0.988 Q80WT2 →
Q8BUR3 — 0.988 Q8BUR3 →
Q2KHR2 — 0.987 Q2KHR2 →
P51774 — 0.987 P51774 →
Q8WYQ9 — 0.987 Q8WYQ9 →