PRDM12 Polyclonal Antibody, 50ul Protein Analysis Mutations in this gene are

Mutations in this gene are associated with interleukin 2 receptor alpha deficiency

FOXA1 encodes a member of the forkhead class of DNA-binding proteins

This protein is a secreted enzyme that is proposed to regulate the availability of insulin-like growth factors (IGFs) by cleaving IGF-binding proteins

This gene encodes a mitochondrial metalloprotease protein that is a member of the AAA family

suggesting its role in diverse biochemical activities related to signal transduction

PRDM12 Polyclonal Antibody, 50ul Protein Analysis Mutations in this gene arePRDM12 (PR Domain 12) is a Protein Coding gene. Diseases associated with PRDM12 include neuropathy, hereditary sensory and autonomic, type viii. Gene Ontology (GO) annotations related to PRDM12 include methyltransferase activity. An important paralog of PRDM12 is PRDM6.