LY65C Rabbit Polyclonal Antibody, 100ul Sampling Tubes Mutations in this gene have

Mutations in this gene have been associated with bare lymphocyte syndrome type II (also known as hereditary MHC class II deficiency or HLA class II-deficient combined immunodeficiency)

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This protein (apoptotic peptidase activating factor 1) contains several copies of the WD-40 domain

The transmembrane protein encoded by this gene (interleukin 17A receptor

LY65C Rabbit Polyclonal Antibody, 100ul Sampling Tubes Mutations in this gene haveLY6G5C belongs to a cluster of leukocyte antigen 6 (LY6) genes located in the major histocompatibility complex (MHC) class III region on chromosome 6. Members of the LY6 superfamily typically contain 70 to 80 amino acids including 8 to 10 cysteines. Most LY6 proteins are attached to the cell surface by a glycosylphosphatidylinositol (GPI) anchor that is directly involved in signal transduction (Mallya et al. 2002