TMEM106B
Description
The TMEM106B gene, located on chromosome 10, encodes a transmembrane protein involved in various cellular processes, including neuronal development and function. While its exact role remains under investigation, its association with several neurological disorders highlights its significance in brain health. TMEM106B is crucial for maintaining neuronal integrity and promoting proper synaptic communication, making it a prime target for understanding and treating neurological diseases.
Associated Diseases
Did you know?
Mutations in TMEM106B have been linked to rare genetic syndromes like Joubert syndrome, a condition characterized by cerebellar malformations and developmental delays.
