CD55 Polyclonal Antibody, 100ul[BT-AP02456] Cell Screening and Imaging Mutations in this gene may

Mutations in this gene may result in Netherton syndrome

and thus represents a nonreceptor-type isoform of this PTP

which is associated with Borjeson-Forssman-Lehmann syndrome (BFLS)

The protein encoded by this gene is a secreted protein that is involved in the regulation of bone development

CD55 Polyclonal Antibody, 100ul[BT-AP02456] Cell Screening and Imaging Mutations in this gene mayCytochrome b5 type A encoded by CYB5A is a membrane bound cytochrome that reduces ferric hemoglobin (methemoglobin) to ferrous hemoglobin, which is required for stearyl CoA desaturase activity. Defects in CYB5A are a cause of type IV hereditary methemoglobinemia. Three transcript variants encoding different isoforms have been found for CYB5A.