Sugi Predict

Sugi Predict / Targets / RHOXF2

RHOXF2

Rhox homeobox family member 2 · Q9BQY4 · RHOXF2 on Sugi Atlas →

0 patent compounds predicted against RHOXF2, 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 RHOXF2 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Safety and Tolerability Study of Gene Editing Drug ZVS203e in Participants With Retinitis Pigmentosa EARLY_PHASE1UNKNOWN
ADRB3, ROCK2 and GEF Levels in Overactive Bladder Patients nanCOMPLETED
Investigating the Genetic Basis of Pseudoexfoliation Syndrome, Angle-closure Glaucoma and Primary Open-angle Glaucoma nanRECRUITING
Study of the Pathophysiological Mechanisms Involved in Bleeding Events nanCOMPLETED
PHF19 Gene Expression and EZH2 Gene Deletion in Acute Myeloid Leukemia nanUNKNOWN
Genomewide Screening of Pathological Myopia nanUNKNOWN
Genetic Basis of Non Syndromic Congenital Diaphragmatic Hernia nanCOMPLETED
Family Myopia Study nanCOMPLETED
Identifying Genes and Mutations Underlying Retinitis Pigmentosa and Allied Diseases nanUNKNOWN
Identification of Genes and Pathogenesis Involved in Familial Thoracic Aortic Aneurysm nanCOMPLETED
Genetic Study of Patients With Primary Ciliary Dyskinesia nanCOMPLETED
Genetic Analysis of Familial Cases of Premature Ovarian Failure nanCOMPLETED
A Study of the Genetic Analysis of Brain Disorders nanCOMPLETED
NCF Gene & TNFSF4 in SLE Patients nanUNKNOWN
X-Chromosome Inactivation Status and Premature Ovarian Failure nanCOMPLETED
Prospective Genetic Study in Patients With Ovarian Insufficiency nanUNKNOWN
Shanghai High Myopia Study nanRECRUITING
Whole-genome Sequencing Study in Patients With Diminished Ovarian Reserve nanUNKNOWN
Gene Mutations and Rescue in Human Congenital Diaphragmatic Hernia nanUNKNOWN
Autophagy in Systemic Lupus Erythematosus nanUNKNOWN
Genetic Characterization of Parkinson's Disease nanCOMPLETED
Molecular Associations With Reproductive Failure nanCOMPLETED
Mapping Disease Pathways for Biliary Atresia nanRECRUITING
Whole Exome and Whole Genome Sequencing for Genotyping of Inherited and Congenital Eye Conditions nanRECRUITING
X-chromosome Inactivation, Epigenetics and the Transcriptome nanCOMPLETED
Studies on the Expression and Functions of RLIP76 in Blood Samples of Healthy Human Subjects nanWITHDRAWN
Chromosome 5Q Gene Variants and Asthma-Related Traits nanCOMPLETED
Identification of an Asthma Susceptibility Gene on 3P nanCOMPLETED
Autoimmune Dysregulation in Pigmentary Glaucoma nanCOMPLETED
Family Blood Pressure Program - GenNet Network nanCOMPLETED

Related proteins — ESM-2 sequence neighbours (a RHOXF2 binder may also engage these)

ProteinNameSimilarity
P0C7M4 — 1.000 P0C7M4 →
P09632 — 0.994 P09632 →
P52954 — 0.994 P52954 →
Q8BG36 — 0.993 Q8BG36 →
Q90655 — 0.993 Q90655 →
Q1KKR7 — 0.993 Q1KKR7 →
Q08727 — 0.992 Q08727 →
P35993 — 0.992 P35993 →
P32442 — 0.992 P32442 →
Q91X45 — 0.991 Q91X45 →
Q9EPW2 — 0.991 Q9EPW2 →
P17483 — 0.991 P17483 →
P52951 — 0.991 P52951 →
P43688 — 0.991 P43688 →
Q9W6D8 — 0.991 Q9W6D8 →
Q9WTP9 — 0.991 Q9WTP9 →
Q8CJE2 — 0.991 Q8CJE2 →
P31311 — 0.990 P31311 →
P52945 — 0.990 P52945 →
P24899 — 0.990 P24899 →
Q7TQG0 — 0.990 Q7TQG0 →
Q804R0 — 0.990 Q804R0 →
P48031 — 0.990 P48031 →
P20263 — 0.990 P20263 →
Q4G112 — 0.990 Q4G112 →
P19091 — 0.990 P19091 →
Q68EH7 — 0.990 Q68EH7 →
P70284 — 0.990 P70284 →
A2D649 — 0.990 A2D649 →
Q9PWD6 — 0.990 Q9PWD6 →