Sugi Predict

Sugi Predict / Targets / GPATCH8

GPATCH8

G patch domain-containing protein 8 · Q9UKJ3 · GPATCH8 on Sugi Atlas →

0 patent compounds predicted against GPATCH8, 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 GPATCH8 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
Safety Evaluation of Gene Therapy in Leber Hereditary Optic Neuropathy (LHON) Patients PHASE1/PHASE2COMPLETED
Clinical Application of PET Imaging Targeting GPA33 in Malignant Tumors nanNOT_YET_RECRUITING
Genetic Study in Patients With Stage II or Stage III Colon Cancer nanCOMPLETED
Characterization of New Candidate Genes in Cases of Human Inherited Thrombocytopenia (CATCH) nanCOMPLETED
Relationship Between Genes Important in Blood Pressure Regulation and Blood Pressure Therapy in Hypertension nanCOMPLETED
Identifying Genes and Mutations Underlying Retinitis Pigmentosa and Allied Diseases nanUNKNOWN
Identification of Genes and Pathogenesis Involved in Familial Thoracic Aortic Aneurysm nanCOMPLETED
Genetics and Psychopathology in the 22q11 Deletion Syndrome nanUNKNOWN
Genetics of Endocrine Tumours - Familial Isolated Pituitary Adenoma - FIPA nanRECRUITING
Clinical and Genetic Studies of VACTERL Association nanCOMPLETED
Chromosome 5Q Gene Variants and Asthma-Related Traits nanCOMPLETED
Role of Polymorphisms in the IL-1 Gene Cluster nanCOMPLETED
Immune Cell Response to Stimuli nanRECRUITING
PACAP Induced Migraine Attacks in Patients With High and Low Genetic Load nanCOMPLETED
Genetic Analysis of Heart Channelopathies in Brazilian Patients and Their Relatives nanUNKNOWN
Markers and Mechanisms of Macrovascular Disease in IDDM nanCOMPLETED
Identification of a New Gene Involved in Hereditary Lipodystrophy nanCOMPLETED
Autophagy in Systemic Lupus Erythematosus nanUNKNOWN
Inherited Reproductive Disorders nanRECRUITING
Exome Analysis in Hearing Impaired Patients nanUNKNOWN
Genetic Characterization of Parkinson's Disease nanCOMPLETED
Whole Exome and Whole Genome Sequencing for Genotyping of Inherited and Congenital Eye Conditions nanRECRUITING
Study of the Genetic and Epigenetic Causes of Recurrent Hydatidiform Moles nanACTIVE_NOT_RECRUITING
Genetic Analysis of Hereditary Disorders of Hearing and Balance nanCOMPLETED
Hereditary Spastic Paraplegia Genomic Sequencing Initiative (HSPseq) nanRECRUITING
Neutrophils as Prognostic Factors in Granulomatosis With Polyangiitis (Formerly Named Wegener's Granulomatosis) nanCOMPLETED
Exploring the Genetics of Neuropathic Pain nanRECRUITING
Global Profiling of Gene and Protein Expression Associated With Coronary Heart Disease Reversal nanCOMPLETED
the Role of plin5 in the Development of Nonalcoholic Fatty Liver Disease. nanUNKNOWN

Related proteins — ESM-2 sequence neighbours (a GPATCH8 binder may also engage these)

ProteinNameSimilarity
A2A6A1 — 1.000 A2A6A1 →
P30415 — 0.991 P30415 →
Q6UB99 — 0.989 Q6UB99 →
P30414 — 0.989 P30414 →
Q14AX6 — 0.988 Q14AX6 →
Q3KPW4 — 0.988 Q3KPW4 →
Q5YCW1 — 0.987 Q5YCW1 →
Q6P9P0 — 0.987 Q6P9P0 →
B0QZF7 — 0.987 B0QZF7 →
MYT1 Myelin transcription factor 1 0.987 landscape →
Q3MJK5 — 0.987 Q3MJK5 →
Q9JIX8 — 0.987 Q9JIX8 →
Q66PJ3 — 0.986 Q66PJ3 →
Q5R6I3 — 0.986 Q5R6I3 →
B0BN49 — 0.986 B0BN49 →
Q7TQC7 — 0.986 Q7TQC7 →
Q96JQ2 — 0.986 Q96JQ2 →
Q8C5W0 — 0.986 Q8C5W0 →
Q9NPI7 — 0.986 Q9NPI7 →
Q6A065 — 0.986 Q6A065 →
P97868 — 0.986 P97868 →
Q8R2M2 — 0.985 Q8R2M2 →
Q9P1A6 — 0.985 Q9P1A6 →
Q9UKL3 — 0.985 Q9UKL3 →
Q66J90 — 0.985 Q66J90 →
Q5S6V2 — 0.985 Q5S6V2 →
Q9D4V4 — 0.985 Q9D4V4 →
P19332 — 0.985 P19332 →
PPHLN1 Periphilin-1 0.985 landscape →
Q3UC65 — 0.985 Q3UC65 →