AASS Polyclonal Antibody, 100ul Miscellaneous This protein is thought to

This protein is thought to be part of a family of integral Golgi membrane proteins

member 17) is a 304 amino acid protein containing a J domain and a RRM (RNA recognition motif) domain

Mutations in RPS19 cause Diamond-Blackfan anemia (DBA)

This complex is composed partly of two structural maintenance of chromosomes (SMC) proteins| SMC3 and either SMC1B or the protein encoded by this gene

This protein was found to associate with

AASS Polyclonal Antibody, 100ul Miscellaneous This protein is thought toAASS encodes a bifunctional enzyme (aminoadipate semialdehyde synthase) that catalyzes the first two steps in the mammalian lysine degradation pathway. The N terminal and the C terminal portions of this enzyme contain lysine ketoglutarate reductase and saccharopine dehydrogenase activity, respectively, resulting in the conversion of lysine to alpha aminoadipic semialdehyde. Mutations in AASS are associated with familial hyperlysinemia.