S10A2 Polyclonal Antibody, 50ul Peptide Modification This gene encodes a member

This gene encodes a member of the 17beta-hydroxysteroid dehydrogenase family of short-chain dehydrogenases/reductases

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Deficiencies lead to the skeletal malformation syndrome campomelic dysplasia

Related pseudogenes are found on chromosomes 3 and 7

S10A2 Polyclonal Antibody, 50ul Peptide Modification This gene encodes a memberThe 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 have a tumor suppressor