Sugi Predict

Sugi Predict / Targets / TWF2

TWF2

Twinfilin-2 · Q6IBS0 · TWF2 on Sugi Atlas →

0 patent compounds predicted against TWF2, 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 TWF2 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Uncovering the Etiologies of Non-immune Hydrops Fetalis nanENROLLING_BY_INVITATION
Exome Analysis in Hearing Impaired Patients nanUNKNOWN
Natural History Evaluation of Charcot Marie Tooth Disease (CMT) Types CMT1B, CMT2A, CMT4A, CMT4C, and Others nanRECRUITING
PCD New Gene Discovery nanCOMPLETED
Characterization of WAGR Syndrome and Other Chromosome 11 Gene Deletions nanCOMPLETED
Genetic Analyses of Nonsyndromic and Syndromic Deafness in Pakistan nanENROLLING_BY_INVITATION
Finding Genes With NGS Techniques in Whom Mutations Cause Neurological Diseases nanUNKNOWN
Diagnosis of Primary Ciliary Dyskinesia nanCOMPLETED
Genetic Basis of Non Syndromic Congenital Diaphragmatic Hernia nanCOMPLETED
I-Tracking Neurodegeneration in Early Wolfram Syndrome nanCOMPLETED
Natural History and Genetic Studies of Usher Syndrome nanCOMPLETED
Whole-genome Sequencing Study in Patients With Diminished Ovarian Reserve nanUNKNOWN
Role of Genetics in Idiopathic Pulmonary Fibrosis (IPF) nanUNKNOWN
Maternal Genes and Epimutations: Beckwith-Wiedemann Syndrome & Reproductive Risks nanRECRUITING
Genetics of Primary Ciliary Dyskinesia nanCOMPLETED
Child Development and Genetic Biomarkers(II): Gene Verification and Data Integration nanUNKNOWN
X-Chromosome Inactivation Status and Premature Ovarian Failure nanCOMPLETED
Identification of a New Gene Involved in Hereditary Lipodystrophy nanCOMPLETED
Molecular Genetic Epidemiology of Endocardial Cushion Defects - SCOR in Pediatric Cardiovascular Disease nanCOMPLETED
Whole Exome and Whole Genome Sequencing for Genotyping of Inherited and Congenital Eye Conditions nanRECRUITING
Pulmonary Hypertension--Mechanisms and Family Registry nanCOMPLETED
Pathogenesis of Primary Ciliary Dyskinesia (PCD) Lung Disease nanRECRUITING
Gene Analysis of Parkinson's Disease nanCOMPLETED
Characterization of New Candidate Genes in Cases of Human Inherited Thrombocytopenia (CATCH) nanCOMPLETED
Biomarkers in SCOTland CardiomyopatHy Registry (Bio-SCOTCH) nanRECRUITING
Epidemiological and Genetic Studies of Body Mass Index nanCOMPLETED
Genetic Analysis of Parkinson's Disease nanCOMPLETED
Study of the Genetic and Epigenetic Causes of Recurrent Hydatidiform Moles nanACTIVE_NOT_RECRUITING
Study of a Candidate Gene Involved in Goldenhar Syndrome. nanCOMPLETED
Delineating the Molecular Spectrum and the Clinical, Imaging and Neuronal Phenotype of Chopra-Amiel-Gordon Syndrome nanRECRUITING

Related proteins — ESM-2 sequence neighbours (a TWF2 binder may also engage these)

ProteinNameSimilarity
Q9Z0P5 — 1.000 Q9Z0P5 →
Q5RFH1 — 1.000 Q5RFH1 →
Q9VFM9 — 0.997 Q9VFM9 →
Q5ZM35 — 0.997 Q5ZM35 →
Q6GMH3 — 0.994 Q6GMH3 →
Q7QG28 — 0.994 Q7QG28 →
Q91YR1 — 0.994 Q91YR1 →
Q298X4 — 0.994 Q298X4 →
Q5I082 — 0.994 Q5I082 →
Q7ZXP0 — 0.993 Q7ZXP0 →
Q5RJR2 — 0.993 Q5RJR2 →
Q640W2 — 0.992 Q640W2 →
Q17A58 — 0.991 Q17A58 →
Q12792 — 0.990 Q12792 →
Q56JV6 — 0.988 Q56JV6 →
Q5R7N2 — 0.988 Q5R7N2 →
Q68F50 — 0.984 Q68F50 →
DSTN Destrin 0.974 landscape →
P60982 — 0.973 P60982 →
Q9VJL6 — 0.972 Q9VJL6 →
NAT10 RNA cytidine acetyltransferase 0.972 landscape →
P18359 — 0.972 P18359 →
Q9R0P5 — 0.971 Q9R0P5 →
Q5E9D5 — 0.971 Q5E9D5 →
Q7M0E3 — 0.969 Q7M0E3 →
P45695 — 0.969 P45695 →
P31669 — 0.969 P31669 →
Q4WK80 — 0.968 Q4WK80 →
O93257 — 0.968 O93257 →
Q803R5 — 0.968 Q803R5 →