STMN3
Description
The STMN3 (stathmin 3) is a protein-coding gene located on chromosome 20.
Stathmin-3 is a protein encoded by the STMN3 gene in humans. It belongs to the stathmin/oncoprotein 18 family of microtubule-destabilizing phosphoproteins. It shares similarities with the SCG10 protein and is involved in signal transduction and regulating microtubule dynamics. Stathmin-3 has been shown to interact with TRPC5.
STMN3 is also known as SCLIP.
Associated Diseases
- Griscelli syndrome type 3
- hereditary persistence of fetal hemoglobin-sickle cell disease syndrome
- hemoglobin D disease
- uncombable hair syndrome
