ATP11A and sensorineural hearing loss disorder: For example, mutations in ATP11A have been found in families with sensorineural hearing loss inherited in an autosomal dominant fashion (Chepurwar et al., 2023; Pater et al., 2022; Vona et al., 2023), while variants near this gene have been linked to severe Covid19 through genome-wide association studies (GWAS) and splicing quantitative trait loci (sQTL) analysis (Kousathanas et al., 2022; Nakanishi et al., 2023).