PSL2Z

PSL2Z is a protein that in humans is encoded by the PSL2 gene. This gene is a member of the PSL family, which includes genes involved in the regulation of cell proliferation and differentiation. The PSL2 gene is located on chromosome 17 and spans about 12 kilobases of DNA.

The protein encoded by PSL2 is a member of the PSL family of proteins, which are involved in the regulation of cell proliferation and differentiation. The PSL2 protein is expressed in various tissues, including the brain, heart, and skeletal muscle. It is thought to play a role in the regulation of cell cycle progression and apoptosis, processes that are crucial for normal development and tissue maintenance.

Mutations in the PSL2 gene have been associated with several neurological and developmental disorders. For example, PSL2 mutations have been linked to intellectual disability, epilepsy, and autism spectrum disorder. Additionally, PSL2 mutations have been found in patients with Charcot-Marie-Tooth disease, a neurological disorder that affects the peripheral nerves.

The exact function of the PSL2 protein is not fully understood, and further research is needed to elucidate its role in health and disease. However, its involvement in cell proliferation and differentiation makes it an interesting target for therapeutic interventions in various conditions.