Tyrosine Hydroxylase Polyclonal Antibody, 100ul Peripheral Blood Separation Tube Defects in NLRP3 may cause

Defects in NLRP3 may cause FCAS1

are nonlysosomal

This gene encodes a member of the NipSnap family of proteins that may be involved in vesicular transport

This gene encodes a member of the RAS-like small GTP-binding protein superfamily

The protein belongs to the L37E family of ribosomal proteins

Tyrosine Hydroxylase Polyclonal Antibody, 100ul Peripheral Blood Separation Tube Defects in NLRP3 may causeThe protein encoded by this gene is involved in the conversion of tyrosine to dopamine. It is the rate limiting enzyme in the synthesis of catecholamines, hence plays a key role in the physiology of adrenergic neurons. Mutations in this gene have been associated with autosomal recessive Segawa syndrome. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene.