TSPEAR


Description

The TSPEAR (thrombospondin type laminin G domain and EAR repeats) is a protein-coding gene located on chromosome 21.

TSPEAR plays a critical role in tooth and hair follicle development by regulating the Notch signaling pathway. It may also be involved in the development or function of the auditory system.

TSPEAR is also known as C21orf29, DFNB98, ECTD14, STHAG10, TSP-EAR.

Associated Diseases


Disclaimer: The information provided here is not exhaustive by any means. Always consult your doctor or other qualified healthcare provider with any questions you may have regarding a medical condition, procedure, or treatment, whether it is a prescription medication, over-the-counter drug, vitamin, supplement, or herbal alternative.