From Wikipedia, the free encyclopedia
Protein-coding gene in the species Homo sapiens
Beta-1,3-glucosyltransferase is an enzyme that in humans is encoded by the B3GALTL gene .[ 5] [ 6] [ 7] [ 8]
^ a b c GRCh38: Ensembl release 89: ENSG00000187676 – Ensembl , May 2017
^ a b c GRCm38: Ensembl release 89: ENSMUSG00000051950 – Ensembl , May 2017
^ "Human PubMed Reference:" . National Center for Biotechnology Information, U.S. National Library of Medicine .
^ "Mouse PubMed Reference:" . National Center for Biotechnology Information, U.S. National Library of Medicine .
^ Heinonen TY, Pasternack L, Lindfors K, Breton C, Gastinel LN, Maki M, et al. (Aug 2003). "A novel human glycosyltransferase: primary structure and characterization of the gene and transcripts". Biochem Biophys Res Commun . 309 (1): 166–174. doi :10.1016/S0006-291X(03)01540-7 . PMID 12943678 .
^ Sato T, Sato M, Kiyohara K, Sogabe M, Shikanai T, Kikuchi N, et al. (Nov 2006). "Molecular cloning and characterization of a novel human beta1,3-glucosyltransferase, which is localized at the endoplasmic reticulum and glucosylates O-linked fucosylglycan on thrombospondin type 1 repeat domain" . Glycobiology . 16 (12): 1194–1206. doi :10.1093/glycob/cwl035 . PMID 16899492 .
^ Kozma K, Keusch JJ, Hegemann B, Luther KB, Klein D, Hess D, et al. (Nov 2006). "Identification and characterization of abeta1,3-glucosyltransferase that synthesizes the Glc-beta1,3-Fuc disaccharide on thrombospondin type 1 repeats" . J Biol Chem . 281 (48): 36742–36751. doi :10.1074/jbc.M605912200 . PMID 17032646 .
^ "Entrez Gene: B3GALTL beta 1,3-galactosyltransferase-like" .
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Lesnik Oberstein SA, Kriek M, White SJ, Kalf ME, Szuhai K, Den Dunnen JT, et al. (2006). "Peters Plus syndrome is caused by mutations in B3GALTL, a putative glycosyltransferase" . Am. J. Hum. Genet . 79 (3): 562–566. doi :10.1086/507567 . PMC 1559553 . PMID 16909395 .