VSTM1 Rabbit Polyclonal Antibody, 100ul Peptide Library Certain mutations in this gene

Certain mutations in this gene resulting in a functionally inadequate enzyme are associated with a rare genetic disorder causing nonspherocytic hemolytic anemia

Pseudogenes of this gene are located on the long arm of chromosomes 11 and 17

which excises the activation peptide and thus generates a heavy chain and a light chain held together by one or more disulfide bonds

The CAN (cerberus and dan) subfamily of BMP antagonists

BNIP2 (BCL2 interacting protein 2) is a member of the BCL2/adenovirus E1B 19 kd-interacting protein (BNIP) family

VSTM1 Rabbit Polyclonal Antibody, 100ul Peptide Library Certain mutations in this gene