ADAMTS-19 Polyclonal Antibody, 50ul Drying & Desiccation Mutations in this gene have

Mutations in this gene have been linked to autosomal dominant and recessive forms of nephrogenic diabetes insipidus

Defects in ARNTL have been linked to infertility

Expression level and methylation status of this gene may be correlated with bone mineral density

Among its related pathways are Activation of cAMP-Dependent PKA and Neuropathic Pain-Signaling in Dorsal Horn Neurons

Alternative splicing results in multiple transcript variants| at least one of which

ADAMTS-19 Polyclonal Antibody, 50ul Drying & Desiccation Mutations in this gene haveADAMTS19 encodes a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motif) protein family. Members of the family share several distinct protein modules, including a propeptide region, a metalloproteinase domain, a disintegrin like domain, and a thrombospondin type 1 (TS) motif. Individual members of this family differ in the number of C terminal TS motifs, and some have unique C terminal domains. The protein encoded by