b3galtl
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  • Official Full Name
  • beta 1,3-galactosyltransferase-like
  • Background
  • The protein encoded by this gene is a beta-1,3-glucosyltransferase that transfers glucose to O-linked fucosylglycans on thrombospondin type-1 repeats (TSRs) of several proteins. The encoded protein is a type II membrane protein. Defects in this gene are a cause of Peters-plus syndrome (PPS).
  • Synonyms
  • B3GALTL; beta 1,3-galactosyltransferase-like; beta-1,3-glucosyltransferase; B3Glc T; B3GTL; B3GlcT; Beta 1,3 galactosyltransferase like; Beta 3 galactosyltransferase like; Beta3GlcT; Galactosyltransferase; GalT; beta 3-glycosyltransferase-like; beta-3-glycosyltransferase-like; UDP-GAL:beta-GlcNAc beta-1,3-galactosyltransferase-like; Gal-T; B3Glc-T; beta3Glc-T
Cat.#:B3GALTL-013HTag:GST
Source (Host):Wheat GermSpecies:Human
Product nameRecombinant Human B3GALTL protein, GST-tagged
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Cat.#:B3GALTL-10098HTag:GST
Source (Host):E. coliSpecies:Human
Product nameRecombinant Human B3GALTL, GST-tagged
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Cat.#:B3GALTL-459HTag:Fc-His
Source (Host):HEK293Species:Human
Product nameRecombinant Human B3GALTL, His tagged
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Cat.#:B3GALTL-2235MTag:His
Source (Host):Mammalian CellsSpecies:Mouse
Product nameRecombinant Mouse B3GALTL Protein
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Cat.#:B3GALTL-1103HCLTag:
Source (Host):HEK293Species:Human
Product nameRecombinant Human B3GALTL cell lysate
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B3GALTL Related Articles

Reis, LM; Semina, EV; et al. Genetics of anterior segment dysgenesis disorders. CURRENT OPINION IN OPHTHALMOLOGY 22:314-324(2011).
Aliferis, K; Marsal, C; et al. A novel nonsense B3GALTL mutation confirms Peters plus syndrome in a patient with multiple malformations and Peters anomaly. OPHTHALMIC GENETICS 31:205-208(2010).