S-100A6 Rabbit Polyclonal Antibody, 20ul Protein Expression GSDMC is a Protein Coding

GSDMC is a Protein Coding gene

Mutations in SLC22A5 (solute carrier family 22 member 5)are the cause of systemic primary carnitine deficiency (CDSP)

It modulates p53 function

The encoded type 2 transmembrane protein may play a role in dendritic cell function

Very large introns typically separate the exons encoding the VPS10 domain

S-100A6 Rabbit Polyclonal Antibody, 20ul Protein Expression GSDMC is a Protein CodingThe protein encoded by this gene is a member of the S100 family of proteins containing 2 EF hand calcium binding motifs. S100 proteins are localized in the cytoplasm and or nucleus of a wide range of cells and involved in the regulation of a number of cellular processes such as cell cycle progression and differentiation. S100 genes include at least 13 members which are located as a cluster on chromosome 1q21. This protein may function in stimulation