Hydropathic AF‐2 variants in the androgen receptor gene among androgen insensitivity patients.

Background Objectives Materials and methods Results Discussion Conclusion Androgen insensitivity syndrome (AIS) is a common condition among individuals with differences of sexual development (DSD) and results from germline allelic variants in the androgen receptor (<italic>AR</italic>) gene. Understanding the phenotypic consequences of <italic>AR</italic> allelic variants that disrupt the activation function 2 (AF2) region is essential to grasping its clinical significance.This study aims to provide insights into the phenotypic characteristics and clinical impact of <italic>AR</italic> mutations affecting the AF2 region in AIS patients. We achieve this by reviewing reported AR variants in the AF2 region among individuals with AIS, including identifying a new phenotype associated with the c.2138T>C variant (p.Leu713Pro) in the <italic>AR</italic> gene.We comprehensively reviewed <italic>AR</italic> variants within the AF2 region reported in AIS and applied molecular dynamics simulations to assess the impact of the p.Leu713Pro variant on protein dynamics.Our review of reported <italic>AR</italic> variants in the AF2 region revealed a spectrum of phenotypic outcomes in AIS patients. Molecular dynamics simulations indicated that the p.Leu713Pro variant significantly alters the local dynamics of the <italic>AR</italic> protein and disrupts the correlation and covariance between variables.The diverse phenotypic presentations observed among individuals with <italic>AR</italic> variants in the AF2 region highlight the complexity of AIS. The altered protein dynamics resulting from the p.Leu713Pro variant further emphasize the importance of the AF2 region in <italic>AR</italic> function.Our study provides valuable insights into AR mutations' phenotypic characteristics and clinical impact on the AF2 region in AIS. Moreover, the disruption of protein dynamics underscores the significance of the AF2 region in AR function and its role in the pathogenesis of AIS. [ABSTRACT FROM AUTHOR]