DACH1

Dachshund homolog 1 · Q9UI36 · DACH1 on Sugi Atlas →

0 patent compounds predicted against DACH1, 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 DACH1 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Pharmacogenetics of Disulfiram for Cocaine PHASE2COMPLETED
A Phase II Study of Bevacizumab and Erlotinib in Subjects With Advanced Hereditary Leiomyomatosis and Renal Cell Cancer (HLRCC) or Sporadic Papillary Renal Cell Cancer PHASE2COMPLETED
Nivolumab With Vismodegib in Patients With Basal Cell Nevus Syndrome PHASE2WITHDRAWN
Phase I Dose Finding and Proof-of-concept Study of Panobinostat With Standard Dose Cytarabine and Daunorubicin for Untreated Acute Myeloid Leukemia or Advanced Myelodysplastic Syndrome PHASE1COMPLETED
Treatment Duration Increment and Pharmacodynamic Study of CX-4945 in Patients With Basal Cell Carcinoma (BCC) PHASE1COMPLETED
FOLFIRINOX Plus IPI-926 for Advanced Pancreatic Adenocarcinoma PHASE1COMPLETED
Phase I Study of Gene Induction Mediated by Sequential Decitabine/Depsipeptide Infusion With or Without Concurrent Celecoxib in Subjects With Pulmonary and Pleural Malignancies PHASE1COMPLETED
The PAH Platform for Deep Phenotyping in Korean Subjects nanUNKNOWN
Diaphragmatic Hernia Research & Exploration, Advancing Molecular Science nanRECRUITING
Genetic Study of Patients With Primary Ciliary Dyskinesia nanCOMPLETED
Pathogenesis of Primary Ciliary Dyskinesia (PCD) Lung Disease nanRECRUITING
Inherited Reproductive Disorders nanRECRUITING
Human Epilepsy Genetics--Neuronal Migration Disorders Study nanRECRUITING
Gene Mutations and Rescue in Human Congenital Diaphragmatic Hernia nanUNKNOWN
Evaluation of rhGH Replacement Therapy in Patients With Pseudohypoparathyroidism Type Ia (PHP Ia) nanUNKNOWN
PCD New Gene Discovery nanCOMPLETED
Genetic Basis of Non Syndromic Congenital Diaphragmatic Hernia nanCOMPLETED
Evaluation of Phenotypic and Genetic Properties in Male Subjects Affected By Hypohidrotic Ectodermal Dysplasia nanCOMPLETED
Hormonal Regulation of Puberty and Fertility nanCOMPLETED
SS-HH-OCT as a Novel Diagnostic Modality for Early-Onset Retinal Dystrophies (EORDs) nanRECRUITING
Whole-genome Sequencing Study in Patients With Diminished Ovarian Reserve nanUNKNOWN
Study of Skeletal Disorders and Short Stature nanCOMPLETED
Genetics of Primary Ciliary Dyskinesia nanCOMPLETED
Inherited Genetic Susceptibility in Langerhans Cell Histiocytosis (LCH) nanACTIVE_NOT_RECRUITING
CDH1 Germline Mutations in Lobular Breast Cancer nanCOMPLETED
X-Linked Hypohidrotic Ectodermal Dysplasia (XLHED) Carrier Outlook Toward Reproduction Survey nanCOMPLETED
Hirschsprung Disease Genetic Study nanRECRUITING
Genetic Clues to Chordoma Etiology: A Protocol to Identify Sporadic Chordoma Patients for Studies of Cancer-Susceptibility Genes nanACTIVE_NOT_RECRUITING
A Study Providing Genetic Testing to Find Those Who May Have Primary Ciliary Dyskinesia for Potential Clinical Trials nanACTIVE_NOT_RECRUITING
PHF19 Gene Expression and EZH2 Gene Deletion in Acute Myeloid Leukemia nanUNKNOWN

Related proteins — ESM-2 sequence neighbours (a DACH1 binder may also engage these)

ProteinNameSimilarity
Q9QYB2 1.000 Q9QYB2 →
Q9VW27 0.998 Q9VW27 →
P40645 0.998 P40645 →
P40647 0.997 P40647 →
Q5RCU4 0.997 Q5RCU4 →
Q03372 0.996 Q03372 →
Q62431 0.995 Q62431 →
Q96NX9 0.995 Q96NX9 →
Q90XB3 0.995 Q90XB3 →
A0A0G2JTZ2 0.995 A0A0G2JTZ2 →
P06602 0.995 P06602 →
Q5QL03 0.995 Q5QL03 →
P22265 0.994 P22265 →
P0CF24 0.994 P0CF24 →
Q6YHU8 0.994 Q6YHU8 →
Q9NSC2 0.994 Q9NSC2 →
Q925Q8 0.994 Q925Q8 →
Q80TZ9 0.994 Q80TZ9 →
Q95RW8 0.994 Q95RW8 →
Q4VYR7 0.994 Q4VYR7 →
O35762 0.994 O35762 →
P16376 0.994 P16376 →
P23899 0.994 P23899 →
A2BEA6 0.994 A2BEA6 →
Q9YGK8 0.994 Q9YGK8 →
Q06453 0.994 Q06453 →
Q58NQ4 0.993 Q58NQ4 →
Q6EUW2 0.993 Q6EUW2 →
Q91660 0.993 Q91660 →
Q9QYE3 0.993 Q9QYE3 →