SLC41A1

Description

The SLC41A1 gene encodes a protein known as solute carrier family 41 member 1. This protein plays a crucial role in maintaining magnesium (Mg2+) balance within cells. Magnesium is an essential mineral involved in hundreds of metabolic processes, from energy production to DNA replication. SLC41A1 facilitates the transport of Mg2+ across cell membranes, ensuring appropriate levels are available for cellular functions. Disruptions in SLC41A1 function can lead to disturbances in Mg2+ homeostasis, contributing to various health issues.

Associated Diseases

• Hypomagnesemia (low blood magnesium levels)
• Hypermagnesemia (high blood magnesium levels)
• Familial hypomagnesemia with seizures and developmental delay

Did you know?

Mutations in the SLC41A1 gene are associated with a rare genetic disorder called familial hypomagnesemia with seizures and developmental delay, highlighting the critical role of this gene in brain development and function.