FAT3
Description
The FAT3 gene encodes a large transmembrane protein, FAT3, playing a crucial role in neuronal development and function. As a member of the cadherin superfamily, FAT3 facilitates cell-cell adhesion and signaling, crucial for establishing proper neuronal connections. Mutations in FAT3 have been linked to various neurological disorders, highlighting its importance in maintaining brain health.
Associated Diseases
- Vanishing White Matter Disease
- Cerebral palsy
- Schizophrenia
- Autism spectrum disorder
- Intellectual disability
Did you know?
FAT3 is one of the largest human genes, spanning over 2 million base pairs!
