SENP6 Polyclonal Antibody, 100ul Stepper Diseases associated with ADRB2 include

Diseases associated with ADRB2 include obesity and asthma

including group 1 metabotropic glutamate receptors

GO annotations related to this gene include transferase activity

Defects in this gene are a cause of familial amyloidosis Finnish type (FAF)

Mutations in this gene are associated with autosomal SCID (severe combined immunodeficiency disease)

SENP6 Polyclonal Antibody, 100ul Stepper Diseases associated with ADRB2 includeUbiquitin like molecules (UBLs), such as SUMO1 (UBL1; MIM 601912), are structurally related to ubiquitin (MIM 191339) and can be ligated to target proteins in a similar manner as ubiquitin. However, covalent attachment of UBLs does not result in degradation of the modified proteins. SUMO1 modification is implicated in the targeting of RANGAP1 (MIM 602362) to the nuclear pore complex, as well as in stabilization of I kappa B alpha (NFKBIA; MIM 164008)