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  1. 1
    "A novel splicing site mutation of the XK gene in a patient with McLeod syndrome."
    Oizumi T., Daimon M., Wada M., Kurita K., Kameda W., Jimbu Y., Susa S., Yamaguchi H., Ohnuma H., Kato T.
    Submitted (MAY-2005) to the EMBL/GenBank/DDBJ databases
    Cited for: NUCLEOTIDE SEQUENCE.
    Category: Sequences.
    Source: UniProtKB/TrEMBL (unreviewed).
  2. 2
    "The Kell and XK proteins of the Kell blood group are not co-expressed in the central nervous system."
    Claperon A., Hattab C., Armand V., Trottier S., Bertrand O., Ouimet T.
    Brain Res. 1147:12-24(2007) [PubMed] [Europe PMC] [Abstract]
    Annotation: In human cortex the results show expression of XK in cortical neurons with an apparent cytoplasmic localization.Imported.
    Source: GeneRIF:7504.

    This publication is mapped to 56 other entries.

  3. 3
    "Phenotypic variability of a distinct deletion in McLeod syndrome."
    Miranda M., Castiglioni C., Frey B.M., Hergersberg M., Danek A., Jung H.H.
    Mov. Disord. 22:1358-1361(2007) [PubMed] [Europe PMC] [Abstract]
    Annotation: Sequence analysis demonstrated a 5 bp deletion in exon 2 of the XK gene in McLeod syndrome.Imported.
    Source: GeneRIF:7504.

    This publication is mapped to 4 other entries.

  4. 4
    "Comprehensive analysis of the genes responsible for neuroacanthocytosis in mood disorder and schizophrenia."
    Shimo H., Nakamura M., Tomiyasu A., Ichiba M., Ueno S., Sano A.
    Neurosci. Res. 69:196-202(2011) [PubMed] [Europe PMC] [Abstract]
    Annotation: This study identified one non-synonymous and one intron variant in mood disorder and schizophrenia subjects respectively in XK.Imported.
    Source: GeneRIF:7504.

    This publication is mapped to 4 other entries.

  5. 5
    "Two McLeod patients with novel mutations in XK."
    Dubielecka P.M., Hwynn N., Sengun C., Lee S., Lomas-Francis C., Singer C., Fernandez H.H., Walker R.H.
    J. Neurol. Sci. 305:160-164(2011) [PubMed] [Europe PMC] [Abstract]
    Annotation: Novel XK protein mutations are reported in two patients who exhibit typical clinical characteristics of McLeod syndrome.Imported.
    Source: GeneRIF:7504.

    This publication is mapped to 4 other entries.

  6. 6
    "A novel XK gene mutation in a Taiwanese family with McLeod syndrome."
    Chen P.Y., Lai S.C., Yang C.C., Lee M.J., Chiu Y.H., Yan S.H., Lu C.S., Yeh T.H.
    J. Neurol. Sci. 340:221-224(2014) [PubMed] [Europe PMC] [Abstract]
    Annotation: study reports the clinical findings and a novel nonsense hemizygous mutation c.154C>T (p.Gln52X) at exon 1 of XK gene in a Taiwanese family with McLeod syndromeImported.
    Source: GeneRIF:7504.

    This publication is mapped to 4 other entries.

  7. 7
    "No evidence of hypermutability in red cells from patients with paroxysmal nocturnal hemoglobinuria using the XK gene."
    Araten D.J., Zamechek L., Halverson G.
    Haematologica 99:e142-4(2014) [PubMed] [Europe PMC] [Abstract]
    Annotation: The XK gene was not linked to hypermutability in red cells from patients with paroxysmal nocturnal hemoglobinuria.Imported.
    Source: GeneRIF:7504.

    This publication is mapped to 4 other entries.

  8. 8
    "Kell and Kx blood group systems."
    Denomme G.A.
    Immunohematology 31:14-19(2015) [PubMed] [Europe PMC] [Abstract]
    Annotation: the expression of KX is critical to normal morphology and null mutations are associated with the McLeod neuroacanthocytosis syndrome.Imported.
    Source: GeneRIF:7504.

    This publication is mapped to 56 other entries.

1 to 8 of 8  Show

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