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Index > Protein center > HMSD(Gene name) > Human
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  • HMSD (Gene name),
  • Minor histocompatibility protein HMSD variant form (Protein name ),  HMSDV_HUMAN from NCBI database.
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  • General Annotation
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  • Antigen Annotation
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  • Gene name:
    HMSD(C18orf53);
    Protein name:
    Minor histocompatibility protein HMSD variant form(HSMD-v);
    Alternative:

    Organism:
    Human (Homo sapiens). 
    General Annotation
    Sub Unit:
    ACC-6 forms a complex with MHC HLA-B*4403.
    Function:
    This allelic splice variant of HMSD is the precursor of the histocompatibility antigen ACC-6. More generally, minor histocompatibility antigens (mHags) refer to immunogenic peptide which, when complexed with MHC, can generate an immune response after recognition by specific T-cells. The peptides are derived from polymorphic intracellular proteins, which are cleaved by normal pathways of antigen processing. The binding of these peptides to MHC class I or class II molecules and its expression on the cell surface can stimulate T-cell responses and thereby trigger graft rejection or graft-versus-host disease (GVHD) after hematopoietic stem cell transplantation from HLA-identical sibling donor. GVHD is a frequent complication after bone marrow transplantation (BMT), due to mismatch of minor histocompatibility antigen in HLA-matched sibling marrow transplants. However, associated with GVHD, a favorable graft-versus-leukemia (GVL) can be induced by donor-recipient disparities in mHags. ACC-6 is presented to the cell surface by MHC HLA-B*4403. This complex specifically elicits donor-cytotoxic T lymphocyte (CTL) reactivity against hematologic malignancies after treatment by HLA-identical allogenic BMT. It induces cell recognition and lysis by CTL. Immunogenicity of most autosomal mHags results from single-nucleotide polymorphisms that cause amino-acid substitutions within epitopes, leading to the differential recognition of peptides between donor and recipient.
    Subcellular Location:
    N/A
    Protein Attributes:
    Sequence length:
    53
    Sequence:
    50:
    MEIFIEVFSH | FLLQLTELTL | NMCLELPTGS | LEKSLMISSQ | VLQIPVANST | 
    53:
    KQR
    3D Structure:
    N/A
    Predicted Eptitope:
    Please Sign in.
    EIAab Sequence  Vaild Sequence:
    Please Sign in.
    Related Databases
    UniGene:
    MIM:
    Uniprot:
     
    FOR
    ELISA Kit for Human HSMD-v
    ELISA Kit for Human HSMD-v
    CLIA Kit for Human HSMD-v
    CLIA Kit for Human HSMD-v
    Polyclonal Antibody for Human HSMD-v
    Polyclonal Antibody for Human HSMD-v
    Monoclonal Antibody for Human HSMD-v
    Monoclonal Antibody for Human HSMD-v
    Protein for Human HSMD-v
    Protein for Human HSMD-v

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    Precision
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    Linearity
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    References
    1. 1.
      "Alternative splicing due to an intronic SNP in HMSD generates a novel minor histocompatibility antigen."
      Kawase T. , Akatsuka Y. , Torikai H. , Morishima S. , Oka A. , Tsujimura A. , Miyazaki M. , Tsujimura K. , Miyamura K. , Ogawa S. , Inoko H. , Morishima Y. , Kodera Y. , Kuzushima K. , Takahashi T.
      Blood110:1055-1063(2007) [PubMed] [Europe PMC] [Abstract]
      [15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: NUCLEOTIDE SEQUENCE [MRNA];FUNCTION;SUBUNIT;TISSUE SPECIFICITY;POLYMORPHISM
    2. 3.
      [15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA]
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