Sugi Predict

Sugi Predict / Targets / DNAH12

DNAH12

Dynein axonemal heavy chain 12 · Q6ZR08 · DNAH12 on Sugi Atlas →

0 patent compounds predicted against DNAH12, 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 DNAH12 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Pharmacogenetics of Disulfiram for Cocaine PHASE2COMPLETED
Functional Studies of Novel Genes Mutated in Primary Ciliary Dyskinesia II: Genotype to Phenotype EARLY_PHASE1COMPLETED
A Study Providing Genetic Testing to Find Those Who May Have Primary Ciliary Dyskinesia for Potential Clinical Trials nanACTIVE_NOT_RECRUITING
Genetics of Primary Ciliary Dyskinesia nanCOMPLETED
Diagnosis of Primary Ciliary Dyskinesia nanCOMPLETED
Genetic Study of Patients With Primary Ciliary Dyskinesia nanCOMPLETED
Pathogenesis of Primary Ciliary Dyskinesia (PCD) Lung Disease nanRECRUITING
Classification, Functional Stratification and Biomarkers in Ciliopathy (CILLICORIRCM) nanCOMPLETED
Early Detection and Characterization of Primary Ciliary Dyskinesia nanUNKNOWN
PCD New Gene Discovery nanCOMPLETED
Research of Therapeutic Targets in the Frame of Nephronophthisis and Renal Associated Ciliopathies nanRECRUITING
Genetic Bases of Neuroendocrine Neoplasms in Mexican Patients nanRECRUITING
Characterizing the Upper Airway Manifestations in Primary Ciliary Dyskinesia and Primary Immunodeficiencies nanCOMPLETED
NIOX VERO Nasal Application in Primary Ciliary Dyskinesia nanCOMPLETED
Whole-genome Sequencing Study in Patients With Diminished Ovarian Reserve nanUNKNOWN
Mapping Disease Pathways for Biliary Atresia nanRECRUITING
Thermal Spa Treatment and Improvement of Primary Ciliary Dyskinesia nanRECRUITING
Core Stability Exercises and Hereditary Ataxia nanCOMPLETED
Clinical and Genetic Analysis in Congenital Hypothyroidism Due to Thyroid Dysgenesis. nanCOMPLETED
Evaluation of Phenotypic and Genetic Properties in Male Subjects Affected By Hypohidrotic Ectodermal Dysplasia nanCOMPLETED
Universal Rare Gene Study: A Registry and Natural History Study of Retinal Dystrophies Associated With Rare Disease-Causing Genetic Variants nanRECRUITING
Genetic Analysis of Hereditary Disorders of Hearing and Balance nanCOMPLETED
Whole Exome and Whole Genome Sequencing for Genotyping of Inherited and Congenital Eye Conditions nanRECRUITING
Biomarker Research in Inherited Movement Disorders nanRECRUITING
WGS of Korean Idiopathic Bronchiectasis nanUNKNOWN
Inbon Errors of Immunity Attending Assiut University Children&Amp;#39;s Hospital: a Single Center Study nanNOT_YET_RECRUITING
Nerve Ultrasound in Acquired and Genetic Sensory Neuronopathies nanNOT_YET_RECRUITING
Study of Skeletal Disorders and Short Stature nanCOMPLETED
Natural History Evaluation of Charcot Marie Tooth Disease (CMT) Types CMT1B, CMT2A, CMT4A, CMT4C, and Others nanRECRUITING
Muscle Tissue Bank for Muscular Dystrophy nanCOMPLETED

Related proteins — ESM-2 sequence neighbours (a DNAH12 binder may also engage these)

ProteinNameSimilarity
Q923J6 — 1.000 Q923J6 →
Q3V0Q1 — 0.997 Q3V0Q1 →
Q63170 — 0.997 Q63170 →
Q8WXX0 — 0.994 Q8WXX0 →
DYNC1H1 Cytoplasmic dynein 1 heavy chain 1 0.992 landscape →
Q9JHU4 — 0.991 Q9JHU4 →
Q8IVF4 — 0.990 Q8IVF4 →
Q9C0G6 — 0.990 Q9C0G6 →
P23098 — 0.990 P23098 →
P38650 — 0.990 P38650 →
F1SC07 — 0.989 F1SC07 →
Q91XQ0 — 0.989 Q91XQ0 →
Q69Z23 — 0.989 Q69Z23 →
P37276 — 0.989 P37276 →
Q9UFH2 — 0.989 Q9UFH2 →
Q8BW94 — 0.989 Q8BW94 →
Q96JB1 — 0.989 Q96JB1 →
Q9MBF8 — 0.988 Q9MBF8 →
Q9P225 — 0.988 Q9P225 →
Q22A67 — 0.988 Q22A67 →
P39057 — 0.987 P39057 →
P0C6F1 — 0.987 P0C6F1 →
Q9SMH3 — 0.987 Q9SMH3 →
M0R8U1 — 0.986 M0R8U1 →
Q8TE73 — 0.986 Q8TE73 →
P78716 — 0.986 P78716 →
Q39565 — 0.986 Q39565 →
Q96DT5 — 0.986 Q96DT5 →
Q39575 — 0.985 Q39575 →
I7M9J2 — 0.983 I7M9J2 →