ARHGAP35

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ARHGAP35: A Key Regulator of Cellular Functions

Description:

ARHGAP35 (Rho GTPase Activating Protein 35) is a crucial protein involved in regulating cellular processes, including cell migration, adhesion, and cytokinesis. It acts as a molecular switch, controlling the activity of Rho GTPases, a family of proteins that play pivotal roles in various cellular functions.

Associated Diseases:

Mutations in ARHGAP35 have been linked to several genetic disorders, including:

• Charcot-Marie-Tooth Disease Type 4C (CMT4C): A progressive neurological condition characterized by weakness and muscle atrophy in the arms, legs, and hands.
• Hereditary Spastic Paraplegia Type 5 (HSP5): A genetic disorder that affects the spinal cord, leading to progressive lower limb weakness and spasticity.
• Intellectual Disability: ARHGAP35 mutations have been associated with intellectual disability and developmental delays in some individuals.

Did you Know ?

According to recent research, mutations in ARHGAP35 are estimated to occur in approximately 1 in 50,000 individuals. This highlights the rarity of ARHGAP35-associated disorders, but also emphasizes the importance of early diagnosis and management.