Loading...
CPXCR1
This gene is one of several genes identified in a region of the X chromosome associated with an X-linked cleft palate (CPX) disorder. The encoded protein contains a motif similar to a motif found in zinc-finger proteins. Mutation analysis of this gene has not revealed any mutation which causes the CPX disorder. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Sep 2011]
Predicted location
Intracellular
Single cell type specificity
Cell type enriched (Early spermatids)
Immune cell specificity
Not detected in immune cells
Cell line specificity
Not detected
More Types Infomation
-
- Species Reactivity: Human
- Application: Dot, WB
Our customer service representatives are available 24 hours a day, from Monday to Sunday. Contact Us
Can't find the products you're looking for? Try to filter in the left sidebar.Filter By Tag
For Research Use Only. Not For Clinical Use.