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  1. 1
    "The DNA sequence of the human X chromosome."
    Ross M.T., Grafham D.V., Coffey A.J., Scherer S., McLay K., Muzny D., Platzer M., Howell G.R., Burrows C., Bird C.P., Frankish A., Lovell F.L., Howe K.L., Ashurst J.L., Fulton R.S., Sudbrak R., Wen G., Jones M.C.
    Bentley D.R.
    Nature 434:325-337(2005) [PubMed] [Europe PMC] [Abstract]
    Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA].
    Category: Sequences.
    Source: UniProtKB/TrEMBL (unreviewed).

    This publication is cited by 2058 other entries.

  2. 2
    "NEDO human cDNA sequencing project focused on splicing variants."
    Wakamatsu A., Yamamoto J., Kimura K., Ishii S., Watanabe K., Sugiyama A., Murakawa K., Kaida T., Tsuchiya K., Fukuzumi Y., Kumagai A., Oishi Y., Yamamoto S., Ono Y., Komori Y., Yamazaki M., Kisu Y., Nishikawa T.
    Isogai T.
    Submitted (OCT-2007) to the EMBL/GenBank/DDBJ databases
    Cited for: NUCLEOTIDE SEQUENCE.
    Category: Sequences.
    Tissue: Brain.
    Source: UniProtKB/TrEMBL (unreviewed).
  3. 3
    Ensembl
    Submitted (DEC-2015) to UniProtKB
    Cited for: IDENTIFICATION.
    Source: UniProtKB/TrEMBL (unreviewed).
  4. 4
    "Subcellular localization of UDP-GlcNAc, UDP-Gal and SLC35B4 transporters."
    Maszczak-Seneczko D., Olczak T., Olczak M.
    Acta Biochim. Pol. 58:413-419(2011) [PubMed] [Europe PMC] [Abstract]
    Category: Subcellular Location.
    Annotation: localization of the UDP-Gal transporter may depend on the presence of the partner splice variantImported.
    Source: GeneRIF:7355.

    This publication is mapped to 8 other entries.

  5. 5
    Category: Pathology & Biotech, Sequences.
    Annotation: Mosaicism of the UDP-galactose transporter SLC35A2 causes a congenital disorder of glycosylation.Imported.
    Source: GeneRIF:7355.

    This publication is mapped to 5 other entries.

  6. 6
    "UDP-Gal/UDP-GlcNAc chimeric transporter complements mutation defect in mammalian cells deficient in UDP-Gal transporter."
    Olczak M., Maszczak-Seneczko D., Sosicka P., Jakimowicz P., Olczak T.
    Biochem. Biophys. Res. Commun. 434:473-478(2013) [PubMed] [Europe PMC] [Abstract]
    Category: Function, Pathology & Biotech.
    Annotation: The data further supports the hypothesis that UGT and NGT cooperate in the UDP-Gal delivery for glycosyltransferases located in the Golgi apparatus.Imported.
    Source: GeneRIF:7355.

    This publication is mapped to 10 other entries.

  7. 7
    Category: Sequences.
    Annotation: De novo mutations in SLC35A2 encoding a UDP-galactose transporter cause early-onset epileptic encephalopathy.Imported.
    Source: GeneRIF:7355.

    This publication is mapped to 5 other entries.

  8. 8
    "Short N-terminal region of UDP-galactose transporter (SLC35A2) is crucial for galactosylation of N-glycans."
    Sosicka P., Jakimowicz P., Olczak T., Olczak M.
    Biochem. Biophys. Res. Commun. 454:486-492(2014) [PubMed] [Europe PMC] [Abstract]
    Category: Function.
    Annotation: The short N-terminal region composed of 35 N-terminal amino-acid residues of UGT was crucial for galactosylation of N-glycans.Imported.
    Source: GeneRIF:7355.

    This publication is mapped to 6 other entries.

  9. 9
    "UDP-galactose (SLC35A2) and UDP-N-acetylglucosamine (SLC35A3) Transporters Form Glycosylation-related Complexes with Mannoside Acetylglucosaminyltransferases (Mgats)."
    Maszczak-Seneczko D., Sosicka P., Kaczmarek B., Majkowski M., Luzarowski M., Olczak T., Olczak M.
    J. Biol. Chem. 290:15475-15486(2015) [PubMed] [Europe PMC] [Abstract]
    Category: Function.
    Annotation: UDP-galactose (SLC35A2) and UDP-N-acetylglucosamine (SLC35A3) Transporters Form Glycosylation-related Complexes with Mannoside Acetylglucosaminyltransferases (Mgats).Imported.
    Source: GeneRIF:7355.

    This publication is mapped to 22 other entries.

1 to 9 of 9  Show
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