| 1 | SLC35A2, SLC35A3
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| UDP-Gal/UDP-GlcNAc chimeric transporter complements mutation defect in mammalian cells deficient in UDP-Gal transporter.
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| Olczak M, Maszczak-Seneczko D, Sosicka P, Jakimowicz P, Olczak T.
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| Biochem Biophys Res Commun 434(3):473-8. doi: 10.1016/j.bbrc.2013.03.098. Epub 2013 Apr 10.
2013
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| 2 | AMRS, SLC35A3
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| Mutations in SLC35A3 cause autism spectrum disorder, epilepsy and arthrogryposis.
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| Edvardson S, Ashikov A, Jalas C, Sturiale L, Shaag A, Fedick A, Treff NR, Garozzo D, Gerardy-Schahn R, Elpeleg O.
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| J Med Genet 50(11):733-9. doi: 10.1136/jmedgenet-2013-101753. Epub 2013 Sep 12.
2013
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| 3 | SLC35A3
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| UDP-N-acetylglucosamine transporter (SLC35A3) regulates biosynthesis of highly branched N-glycans and keratan sulfate.
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| Maszczak-Seneczko D, Sosicka P, Olczak T, Jakimowicz P, Majkowski M, Olczak M.
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| J Biol Chem 288(30):21850-60. doi: 10.1074/jbc.M113.460543. Epub 2013 Jun 13.
2013
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| 4 | SLC35A2, SLC35A3
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| UDP-N-acetylglucosamine transporter and UDP-galactose transporter form heterologous complexes in the Golgi membrane.
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| Maszczak-Seneczko D, Sosicka P, Majkowski M, Olczak T, Olczak M.
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| FEBS Lett 586(23):4082-7. doi: 10.1016/j.febslet.2012.10.016. Epub 2012 Oct 23.
2012
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| 5 | SLC35A3
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| Evaluation of SLC35A3 as a candidate gene for human vertebral malformations.
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| Ghebranious N, Burmester JK, Glurich I, McPherson E, Ivacic L, Kislow J, Rasmussen K, Kumar V, Raggio CL, Blank RD, Jacobsen FS, Faciszewski T, Womack J, Giampietro PF.
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| Am J Med Genet A 140(12):1346-8. No abstract available. 2006
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| 6 | SLC35A3
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| A missense mutation in the bovine SLC35A3 gene, encoding a UDP-N-acetylglucosamine transporter, causes complex vertebral malformation.
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| Thomsen B, Horn P, Panitz F, Bendixen E, Petersen AH, Holm LE, Nielsen VH, Agerholm JS, Arnbjerg J, Bendixen C.
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| Genome Res 16(1):97-105. Epub 2005 Dec 12. 2006
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| 7 | SLC35A2, SLC35A3
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| Molecular cloning and functional expression of the human golgi UDP-N-acetylglucosamine transporter.
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| Ishida N, et al.
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| J Biochem (Tokyo) 126(1):68-77 1999
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