FAT3

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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!