GNS Polyclonal Antibody, 100ul Metabolic enzymes Other family members are known

Other family members are known to function in post-transcriptional regulation

Tissue-specific processing may lead to the formation in some tissues of larger forms of neuromedin N and neurotensin

The protein encoded by this gene belongs to the aldehyde dehydrogenase family

is a lysosomal cysteine proteinase that may play an important role in corneal physiology

This gene encodes a member of the high sulfur-type keratin-associated protein (KAP) family

GNS Polyclonal Antibody, 100ul Metabolic enzymes Other family members are knownThe product of this gene is a lysosomal enzyme found in all cells. It is involved in the catabolism of heparin, heparan sulphate, and keratan sulphate. Deficiency of this enzyme results in the accumulation of undegraded substrate and the lysosomal storage disorder mucopolysaccharidosis type IIID (Sanfilippo D syndrome). Mucopolysaccharidosis type IIID is the least common of the four subtypes of Sanfilippo syndrome.