RPH3L Rabbit Polyclonal Antibody, 100ul sgRNA Library Construction Mutations in this gene are

Mutations in this gene are associated with inherited venous malformations of the skin and mucous membranes

This protein is also involved in assembly of human cytomegalovirus (HCMV) by interacting with the cellular protein Bicaudal D1

Mutations in RPS19 cause Diamond-Blackfan anemia (DBA)

The protein encoded by this gene is a member of a small family of proteins which bind single stranded DNA/RNA

The protein encoded by this gene is a member of the Borg (binder of Rho GTPases) family of CDC42 effector proteins

RPH3L Rabbit Polyclonal Antibody, 100ul sgRNA Library Construction Mutations in this gene areThe protein encoded by this gene plays a direct regulatory role in calcium ion dependent exocytosis in both endocrine and exocrine cells and plays a key role in insulin secretion by pancreatic cells. This gene is likely a tumor suppressor. Alternative splicing results in multiple transcript variants encoding distinct isoforms.