POMT2 Rabbit Polyclonal Antibody, 100ul Immune Cell Preparation Graves disease

Graves disease

A pseudogene on chromosome 11 has also been characterized

however| imprinting of the human gene may be polymorphic| as only a minority of individuals showed biased expression from the maternal allele (PMID:8267611)

This member of the synapsin family plays a role in regulation of axonogenesis and synaptogenesis

are structurally related to ubiquitin (MIM 191339) and can be ligated to target proteins in a similar manner as ubiquitin

POMT2 Rabbit Polyclonal Antibody, 100ul Immune Cell Preparation Graves diseaseThe protein encoded by this gene is an O mannosyltransferase that requires interaction with the product of the POMT1 gene for enzymatic function. The encoded protein is found in the membrane of the endoplasmic reticulum. Defects in this gene are a cause of Walker Warburg syndrome (WWS).