Sugi Predict

Sugi Predict / Targets / WASHC4

WASHC4

WASH complex subunit 4 · Q2M389 · WASHC4 on Sugi Atlas →

0 patent compounds predicted against WASHC4, 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 WASHC4 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Melpida: Recombinant Adeno-associated Virus (serotype 9) Encoding a Codon Optimized Human AP4M1 Transgene (hAP4M1opt) PHASE1/PHASE2RECRUITING
Open Label Study of Everolimus (RAD001) in Patients With Segmental Overgrowth Syndrome PHASE2WITHDRAWN
Temsirolimus and Sorafenib in Advanced Hepatocellular Carcinoma PHASE1COMPLETED
Susceptibility Genes in Autism Spectrum Disorders nanCOMPLETED
Immune Cell Response to Stimuli nanRECRUITING
Genetic Characterization of Parkinson's Disease nanCOMPLETED
Study of the Pathophysiological Mechanisms Involved in Bleeding Events nanCOMPLETED
Delineating the Molecular Spectrum and the Clinical, Imaging and Neuronal Phenotype of Chopra-Amiel-Gordon Syndrome nanRECRUITING
Maternal Genes and Epimutations: Beckwith-Wiedemann Syndrome & Reproductive Risks nanRECRUITING
Molecular Diagnosis of Syndromic or Isolated Severe Intellectual Disability Using Whole Exome Sequencing : a Pilot Study nanCOMPLETED
Classification, Functional Stratification and Biomarkers in Ciliopathy (CILLICORIRCM) nanCOMPLETED
Exome Analysis in Hearing Impaired Patients nanUNKNOWN
Genetics and Psychopathology in the 22q11 Deletion Syndrome nanUNKNOWN
Regulation of Lymphocyte Anti-tumor Response in Metastatic Patients Treated With the mTOR Inhibitor Everolimus nanCOMPLETED
Child Development and Genetic Biomarkers(II): Gene Verification and Data Integration nanUNKNOWN
Genetic Investigation of Cancer Predisposition nanNOT_YET_RECRUITING
Study to Investigate Genetic Causes of Severe Early Childhood Onset Obesity. nanRECRUITING
Characterization of New Candidate Genes in Cases of Human Inherited Thrombocytopenia (CATCH) nanCOMPLETED
Family Blood Pressure Program - GenNet Network nanCOMPLETED
Whole Exome and Whole Genome Sequencing for Genotyping of Inherited and Congenital Eye Conditions nanRECRUITING
Autophagy in Systemic Lupus Erythematosus nanUNKNOWN
Gene Expression in Inflammatory Bowel Disease nanENROLLING_BY_INVITATION
Identification of a New Gene Involved in Hereditary Lipodystrophy nanCOMPLETED
Mapping Novel Disease Genes for Dilated Cardiomyopathy nanCOMPLETED
Microarray Analysis in Syndromic Obesity nanCOMPLETED
PCD New Gene Discovery nanCOMPLETED
Identification of an Asthma Susceptibility Gene on 3P nanCOMPLETED
Chromosome 5Q Gene Variants and Asthma-Related Traits nanCOMPLETED
Williams Syndrome (WS) and Supravalvar Aortic Stenosis (SVAS) DNA and Tissue Bank nanCOMPLETED
Prevalence and Risk Factors of Nephrocalcinosis in Children at Sohag University Hospital nanUNKNOWN

Related proteins — ESM-2 sequence neighbours (a WASHC4 binder may also engage these)

ProteinNameSimilarity
Q3UMB9 — 1.000 Q3UMB9 →
Q45VK7 — 0.979 Q45VK7 →
Q9JJ79 — 0.977 Q9JJ79 →
Q8NCM8 — 0.977 Q8NCM8 →
Q5R5P0 — 0.975 Q5R5P0 →
Q5RFD3 — 0.973 Q5RFD3 →
Q7ZVM1 — 0.973 Q7ZVM1 →
O54921 — 0.973 O54921 →
Q9D4H1 — 0.972 Q9D4H1 →
Q3UVG3 — 0.972 Q3UVG3 →
P97878 — 0.971 P97878 →
Q6GQ80 — 0.971 Q6GQ80 →
O00507 — 0.971 O00507 →
Q6GQD0 — 0.971 Q6GQD0 →
Q96KP1 — 0.970 Q96KP1 →
Q56A27 — 0.970 Q56A27 →
Q7T322 — 0.970 Q7T322 →
Q5ZHV2 — 0.969 Q5ZHV2 →
Q658Y4 — 0.969 Q658Y4 →
Q640K3 — 0.969 Q640K3 →
Q6TEP1 — 0.969 Q6TEP1 →
Q7TMY8 — 0.969 Q7TMY8 →
Q4R4V3 — 0.969 Q4R4V3 →
P28660 — 0.969 P28660 →
WASHC5 WASH complex subunit 5 0.969 landscape →
C0H906 — 0.968 C0H906 →
Q5XPI4 — 0.968 Q5XPI4 →
Q86UW7 — 0.968 Q86UW7 →
F8VPU6 — 0.968 F8VPU6 →
Q6DIE2 — 0.968 Q6DIE2 →