Search Results for: GLA

13 interactions involving GLA - galactosidase alpha found:

Interactant Symbol Name
Associated Pathways
Binding Drugs
Associated Diseases
ANKRD30A ankyrin repeat domain 30A
CCR2 C-C motif chemokine receptor 2
  • Beta defensins
  • Chemokine receptors bind chemokines
  • G alpha (i) signalling events
  • Interleukin-10 signaling
  • INCB3284
  • CCX915
  • Plozalizumab
COL4A5 collagen type IV alpha 5 chain
  • Collagen degradation
  • Collagen degradation
  • Extracellular matrix organization
  • Collagen biosynthesis and modifying enzymes
  • Signaling by PDGF
  • Assembly of collagen fibrils and other multimeric structures
  • Integrin cell surface interactions
  • Integrin cell surface interactions
  • Anchoring fibril formation
  • Crosslinking of collagen fibrils
  • Laminin interactions
  • Laminin interactions
  • Non-integrin membrane-ECM interactions
  • ECM proteoglycans
  • NCAM1 interactions
  • Collagen chain trimerization
  • Regulation of expression of SLITs and ROBOs
  • Alport syndrome
DUSP6 dual specificity phosphatase 6
  • RAF-independent MAPK1/3 activation
  • ERKs are inactivated
  • Negative regulation of MAPK pathway
GPR17 G protein-coupled receptor 17
  • Leukotriene receptors
  • G alpha (q) signalling events
  • P2Y receptors
  • G alpha (i) signalling events
GUCY2F guanylate cyclase 2F, retinal
  • Inactivation, recovery and regulation of the phototransduction cascade
HNRNPH2 heterogeneous nuclear ribonucleoprotein H2
  • mRNA Splicing - Major Pathway
  • Processing of Capped Intron-Containing Pre-mRNA
MORF4L2 mortality factor 4 like 2
  • HATs acetylate histones
NAP1L3 nucleosome assembly protein 1 like 3
NOSTRIN nitric oxide synthase trafficking
  • NOSTRIN mediated eNOS trafficking
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)
PLP1 proteolipid protein 1
  • Hereditary spastic paraplegia (SPG)
  • Hypomyelinating leukodystrophy (HLD); Pelizaeus-Merzbacher disease (PMD)
TERT telomerase reverse transcriptase
  • Telomere Extension By Telomerase
  • Formation of the beta-catenin:TCF transactivating complex
  • Zidovudine
  • Grn163l
  • Tertomotide
  • Cri du chat syndrome; Cat cry syndrome; Chromosme 5p deletion syndrome