Sugi Predict

Sugi Predict / Targets / PITHD1

PITHD1

PITH domain-containing protein 1 · Q9GZP4 · PITHD1 on Sugi Atlas →

0 patent compounds predicted against PITHD1, 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 PITHD1 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Study of the Anti-FGF23 Antibody, Burosumab, in Adults With XLH PHASE3COMPLETED
The Antibiotic Rifampin to Reduce High Levels of Blood and Urine Calcium in IIH PHASE1UNKNOWN
Inherited Reproductive Disorders nanRECRUITING
Incidence of cCPHD in Denmark - a National Observational Study nanUNKNOWN
Natural History of Photoreceptor Degeneration in USH1B: Clinical Parameters and Validation of Functional Vision Tests in MYO7A nanRECRUITING
Classification, Functional Stratification and Biomarkers in Ciliopathy (CILLICORIRCM) nanCOMPLETED
Hormonal Regulation of Puberty and Fertility nanCOMPLETED
Epidemiology of Pituitary Tumours: Prevalence of Associated Neoplasia nanUNKNOWN
Human Epilepsy Genetics--Neuronal Migration Disorders Study nanRECRUITING
SS-HH-OCT as a Novel Diagnostic Modality for Early-Onset Retinal Dystrophies (EORDs) nanRECRUITING
X-Linked Hypohidrotic Ectodermal Dysplasia (XLHED) Carrier Outlook Toward Reproduction Survey nanCOMPLETED
Investigation of the Genetic Causes of Kallmann Syndrome and Reproductive Disorders nanCOMPLETED
Evaluation of Phenotypic and Genetic Properties in Male Subjects Affected By Hypohidrotic Ectodermal Dysplasia nanCOMPLETED
Clinical and Genetic Analysis in Congenital Hypothyroidism Due to Thyroid Dysgenesis. nanCOMPLETED
Genetic Analysis of Hereditary Disorders of Hearing and Balance nanCOMPLETED
Evaluation of rhGH Replacement Therapy in Patients With Pseudohypoparathyroidism Type Ia (PHP Ia) nanUNKNOWN
Investigating the Genetic Basis of Pseudoexfoliation Syndrome, Angle-closure Glaucoma and Primary Open-angle Glaucoma nanRECRUITING
Identifying Genes and Mutations Underlying Retinitis Pigmentosa and Allied Diseases nanUNKNOWN
Whole Exome and Whole Genome Sequencing for Genotyping of Inherited and Congenital Eye Conditions nanRECRUITING
Drivers of Hypoxia-induced Angiogenesis in Tumor Development nanUNKNOWN
Whole Transcriptome Profiling and Metabolic Phenotyping in Children With ROHHAD Syndrome nanRECRUITING
Natural History and Genetic Studies of Usher Syndrome nanCOMPLETED
Hypophosphatemic Rickets in Norway nanUNKNOWN
Defining the Genetic Basis for the Development of Primary Pigmented Nodular Adrenocortical Disease (PPNAD) and the Carney Complex nanCOMPLETED
Genes Associated With Development of Pulmonary Arterial Hypertension in Patients With Congenital Shunt Lesions nanRECRUITING
Genetics of Endocrine Tumours - Familial Isolated Pituitary Adenoma - FIPA nanRECRUITING
Molecular Analysis of Microphthalmia/Anophthalmia nanCOMPLETED
Genetics of Primary Ciliary Dyskinesia nanCOMPLETED
New Strategies of Genetic Study of Patients With Oculocutaneous Albinism nanCOMPLETED
Stone Disease in Children and Their Families nanCOMPLETED

Related proteins — ESM-2 sequence neighbours (a PITHD1 binder may also engage these)

ProteinNameSimilarity
Q8BWR2 — 1.000 Q8BWR2 →
Q6NYX8 — 0.996 Q6NYX8 →
Q6DJI5 — 0.995 Q6DJI5 →
Q95ZI6 — 0.988 Q95ZI6 →
Q29L80 — 0.988 Q29L80 →
Q9VK68 — 0.985 Q9VK68 →
Q54Z24 — 0.978 Q54Z24 →
Q9P7A1 — 0.978 Q9P7A1 →
Q5E9A6 — 0.973 Q5E9A6 →
O93257 — 0.972 O93257 →
Q920J4 — 0.971 Q920J4 →
Q8VXX0 — 0.971 Q8VXX0 →
Q9BRG1 — 0.970 Q9BRG1 →
Q8CDN6 — 0.970 Q8CDN6 →
Q24087 — 0.970 Q24087 →
TXNL1 Thioredoxin-like protein 1 0.970 landscape →
Q9W3C1 — 0.970 Q9W3C1 →
Q9M2Q4 — 0.970 Q9M2Q4 →
Q9VUL1 — 0.969 Q9VUL1 →
NAT10 RNA cytidine acetyltransferase 0.969 landscape →
Q8WYJ6 — 0.969 Q8WYJ6 →
Q8R307 — 0.969 Q8R307 →
Q66I84 — 0.969 Q66I84 →
Q6NUA1 — 0.969 Q6NUA1 →
O16216 — 0.968 O16216 →
Q8CGK3 — 0.968 Q8CGK3 →
Q9H223 — 0.968 Q9H223 →
Q5PQR5 — 0.968 Q5PQR5 →
O89040 — 0.968 O89040 →
Q9CQN1 — 0.968 Q9CQN1 →