PORIM Polyclonal Antibody, 100ul Fluorescent Staining This gene encodes a member

This gene encodes a member of the Wiskott-Aldrich syndrome (WAS) protein family

amenorrhea and disordered steroidogenesis

Belongs to the thymidine kinase family

Himmelfarb et al

Mutations in this gene have been associated with individuals affected by severe intellectual disability| early-onset epilepsy| microcephaly| congenital cataracts| growth retardation| and spasticity (PMID: 25439727)

PORIM Polyclonal Antibody, 100ul Fluorescent Staining This gene encodes a memberThis gene encodes a highly glycosylated transmembrane protein with a high content of threonine and serine residues in its extracellular domain, similar to a broadly defined category of proteins termed mucins. Exposure of some cell types to anti PORIMIN (pro oncosis receptor inducing membrane injury) antibody, crosslinks this protein on the cell surface and induces a type of cell death termed oncosis. Oncosis is distinct from apoptosis and is