Search Results for: THTPA

8 interactions involving THTPA - thiamine triphosphatase found:

Sort by: Symbol Number of Pathways Number of Drugs Number of Diseases
Novel Symbol Description Pathways Hide Drugs Hide Diseases Hide
Novel DPAGT1 dolichyl-phosphate N-acetylglucosaminephosphotransferase 1
  • Biosynthesis of the N-glycan precursor (dolichol lipid-linked oligosaccharide, LLO) and transfer to a nascent protein
  • Defective DPAGT1 causes CDG-1j, CMSTA2
  • Congenital disorders of glycosylation (CDG) type I
Novel GCDH glutaryl-CoA dehydrogenase
  • Lysine catabolism
  • Flavin adenine dinucleotide
  • S-4-Nitrobutyryl-CoA
  • Glutaric acidemia; Glutaric acidemia, type I (GA1); Glutaric acidemia, type II (GA2); Multiple acyl coenzyme A dehydrogenase deficiency
Novel HEY1 hes related family bHLH transcription factor with YRPW motif 1
  • NOTCH1 Intracellular Domain Regulates Transcription
  • Constitutive Signaling by NOTCH1 PEST Domain Mutants
  • Constitutive Signaling by NOTCH1 HD+PEST Domain Mutants
  • RUNX2 regulates osteoblast differentiation
  • NOTCH3 Intracellular Domain Regulates Transcription
  • NOTCH4 Intracellular Domain Regulates Transcription
  • Cardiogenesis
Novel METTL17 methyltransferase like 17
Novel OR4K5 olfactory receptor family 4 subfamily K member 5
  • Expression and translocation of olfactory receptors
Novel PDE6B phosphodiesterase 6B
  • Activation of the phototransduction cascade
  • Activation of the phototransduction cascade
  • Inactivation, recovery and regulation of the phototransduction cascade
  • Ca2+ pathway
  • Ca2+ pathway
  • Caffeine
  • Trapidil
  • Congenital stationary night blindness (CSNB), including: CSNB type 1 (CSNB1); CSNB type 2 (CSNB2); CSNB autosomal dominant (CSNBAD); Oguchi disease/ CSNB Oguchi type (CSNBO)
  • Retinitis pigmentosa (RP)
Novel RNASE7 ribonuclease A family member 7
  • Antimicrobial peptides
TLX3 T cell leukemia homeobox 3
  • Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia)

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