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SOST

Sclerostin is a secreted glycoprotein with a C-terminal cysteine knot-like (CTCK) domain and sequence similarity to the DAN (differential screening-selected gene aberrative in neuroblastoma) family of bone morphogenetic protein (BMP) antagonists. Loss-of-function mutations in this gene are associated with an autosomal-recessive disorder, sclerosteosis, which causes progressive bone overgrowth. A deletion downstream of this gene, which causes reduced sclerostin expression, is associated with a milder form of the disorder called van Buchem disease.
SOST
Protein class

Disease related genes, FDA approved drug targets, Human disease related genes

Predicted location

Secreted

Single cell type specificity

Cell type enhanced (Collecting duct cells, B-cells)

Immune cell specificity

Not detected in immune cells

Cell line specificity

Group enriched (HaCaT, SuSa)

Interaction

Interacts with LRP4 (via the extracellular domain); the interaction facilitates the inhibition of Wnt signaling. Interacts with LRP5 (via the first two YWTD-EGF repeat domains); the interaction inhibits Wnt-mediated signaling. Interacts with LRP6.

Molecular function

Heparin-binding

More Types Infomation

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For Research Use Only. Not For Clinical Use.

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