56C>T A19V Recessive New   c.85G>A G29S Recessive Sahakitrungruang et al. [26]   c.761G>A R254Q Dominant Savelkoul et al. [28]  Deletion mutations   c.127_128delCA FS/105X Recessive Tajima et al. [27]   c.750delG FS/334X Dominant New   c.775delC FS/334X Dominant New Previously analyzed  Deletion mutations   c.721delG FS/334X Dominant Kuwahara et al. [12]   c.763–772del

FS/331X Dominant Kuwahara et al. [12]   c.812–818del FS/332X Dominant Kuwahara et al. [12] The family trees and results of mutation analysis of newly analyzed families are summarized in Fig. 1. In family 1, two missense mutations (A19V and G29S) were compound heterozygous in a male NDI KU55933 mw patient and manifested by vasopressin-unresponsive polyuria (8–10 L/day). The patient’s

parents were asymptomatic. The father carried a novel A19V mutation, while the mother had a G29S mutation, which was previously reported to be causative [26]. In family 2, the G29S mutation (the same one found in family 1) was homozygous in the proband, and his healthy mother and brother were heterozygous for the mutation. The patient Ilomastat concentration exhibited polyuria (urine volume was 10–15 L/day), and the urine osmolality did not respond to Belnacasan solubility dmso vasopressin (maximum urine osmolality was about 100 mOsm/L). The appearance of NDI symptoms only when the mutations are compound heterozygous or homozygous strongly indicates that these two missense mutations are disease causative. Fig. 1 AOP2 mutations newly found in Japanese NDI families. Six different AQP2 mutations were found in six Japanese NDI families. NA gene analysis not available. *Showing NDI symptoms In family 3, a homozygous 2-nucleotide deletion mutation (c.127_128delCA) was found in a neonatal boy who exhibited polyuria and dehydration. His urine osmolality did not respond to vasopressin (< 150 mOsm/L). Transmembrane Transproters inhibitor The resultant frame shift predicts new amino acids starting at codon 43, with a premature stop at codon 105. The same mutation was found in an unrelated Japanese family and has been reported by others [27]. In family

4, a monoallelic R254Q mutation was found in two siblings and their father. The father and paternal relatives had NDI symptoms, but have not been clinically examined. The siblings (a 1-year-old boy and a 3-year-old girl) showed similar clinical characteristics of polyuria and polydipsia starting 4–6 months after birth, and slight responsiveness of urine osmolality to vasopressin (maximum urine osmolality was about 500 mOsm/L after vasopressin administration). Consistent with these observation, this mutation (R254Q) was recently reported as an NDI causative mutation with dominant inheritance [28]. Another missense mutation on this residue, R254L, was also reported to cause a similar NDI phenotype [29].