Search Results for: USP54

100 interactions involving USP54 - ubiquitin specific peptidase 54 found:

Sort by: Symbol Number of Pathways Number of Drugs Number of Diseases
Novel Interactant Symbol Name
Associated Pathways
Binding Drugs
Associated Diseases
Novel ARID5B AT-rich interaction domain 5B
  • HDMs demethylate histones
Novel CDK19 cyclin dependent kinase 19
  • PPARA activates gene expression
  • Transcriptional regulation of white adipocyte differentiation
  • Transcriptional regulation of white adipocyte differentiation
Novel CFAP70 cilia and flagella associated protein 70
Novel COMTD1 catechol-O-methyltransferase domain containing 1
  • S-adenosyl-L-homocysteine
  • Sinapoyl coenzyme A
  • Feruloyl Coenzyme A
Novel FAM149B1 family with sequence similarity 149 member B1
Novel FUT11 fucosyltransferase 11
  • Lewis blood group biosynthesis
Novel HK1 hexokinase 1
  • Defective HK1 causes hexokinase deficiency (HK deficiency)
  • Glycolysis
  • alpha-D-glucose 6-phosphate
  • Beta-D-Glucose
  • Phosphoaminophosphonic Acid-Adenylate Ester
  • Lonidamine
  • Anemia due to disorders of glycolytic enzymes, including: Hexokinase (HK) deficiency; Phosphoglycerate kinase 1 (PGK1) deficiency; Triose-phosphate isomerase (TPI) deficiency; Glucose phosphate isomerase (GPI) deficiency; Bisphosphoglycerate mutase (BPGM) deficiency
Novel MSS51 MSS51 mitochondrial translational activator
Novel MSX2 msh homeobox 2
  • Regulation of RUNX2 expression and activity
  • Enlarged parietal foramina/cranium bifidum
  • Craniosynostosis, including: Pfeiffer syndrome; Apert syndrome; Crouzon syndrome; Jackson-Weiss syndrome; Beare-Stevenson syndrome; Muenke craniosynostosis; Saethre-Chotzen syndrome; Craniosynostosis Boston type; Antley-Bixler syndrome; Carpenter syndrome; Craniofrontonasal dysplasia; Noonan syndrome; Baller-Gerold syndrome
Novel PLCD1 phospholipase C delta 1
  • Synthesis of IP3 and IP4 in the cytosol
  • 1D-myo-inositol 1,4,5-trisphosphate
  • Inositol 2,4,5-trisphosphate
Novel SAMD8 sterile alpha motif domain containing 8
  • Sphingolipid de novo biosynthesis
Novel TTYH1 tweety family member 1
ANKRD11 ankyrin repeat domain 11
ANKS1A ankyrin repeat and sterile alpha motif domain containing 1A
ARMC7 armadillo repeat containing 7
ATN1 atrophin 1
  • Regulation of PTEN gene transcription
  • Dentatorubropallidoluysian atrophy (DRPLA)
ATXN1 ataxin 1
  • Spinocerebellar ataxia (SCA); Machado-Joseph disease (SCA3)
ATXN1L ataxin 1 like
ATXN7L2 ataxin 7 like 2
BFSP2 beaded filament structural protein 2

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