NRIP3 Polyclonal Antibody, 50ul In vitro Assessment Loss-of-function mutations in SOST are

Loss-of-function mutations in SOST are associated with an autosomal-recessive disorder

The encoded protein is localized to the brush border membrane of the intestinal epithelium and mediates the uptake of di- and tripeptides from the lumen into the enterocytes

The enzymatic activity is under the control of several hormones

This gene may be downstream in the WNT1 signaling pathway that is relevant to malignant transformation

the encoded protein may regulate differentiation

NRIP3 Polyclonal Antibody, 50ul In vitro Assessment Loss-of-function mutations in SOST areNRIP3 (Nuclear Receptor Interacting Protein 3) is a Protein Coding gene. Gene Ontology (GO) annotations related to NRIP3 include aspartic type endopeptidase activity. An important paralog of NRIP3 is NRIP2.