Human | NPHP4 | 261734 | nephronophthisis 4 | |
Human | FOXP3 | 50943 | forkhead box P3 | |
Human | NPHP3 | 27031 | nephronophthisis 3 (adolescent) | |
Human | PTPN22 | 26191 | protein tyrosine phosphatase, non-receptor type 22 (lymphoid) | |
Human | CLDN16 | 10686 | claudin 16 | Presenting symptoms - recurrent UTI, polyuria/polydipsia, hematuria, and abacterial leukocyturia |
Human | SH2B3 | 10019 | SH2B adaptor protein 3 | |
Human | HNF1A | 6927 | HNF1 homeobox A | |
Human | SLC12A3 | 6559 | solute carrier family 12 (sodium/chloride transporter), member 3 | |
Human | SLC5A2 | 6524 | solute carrier family 5 (sodium/glucose cotransporter), member 2 | |
Human | OAS1 | 4938 | 2'-5'-oligoadenylate synthetase 1, 40/46kDa | |
Human | NPHP1 | 4867 | nephronophthisis 1 (juvenile) | |
Human | KCNJ1 | 3758 | potassium inwardly-rectifying channel, subfamily J, member 1 | |
Human | ITPR3 | 3710 | inositol 1,4,5-trisphosphate receptor, type 3 | |
Human | HLA-DQB1 | 3119 | | |
Human | HCRTR2 | 3062 | hypocretin (orexin) receptor 2 | Title:Association of an orexin 1 receptor 408Val variant with polydipsia-hyponatremia in schizophrenic subjects.|Association:Not Found|Conclusion:Our preliminary data suggest that mutation carriers might have an increased susceptibility to polydipsia through an undetermined mechanism. |
Human | HCRTR1 | 3061 | hypocretin (orexin) receptor 1 | Title:Association of an orexin 1 receptor 408Val variant with polydipsia-hyponatremia in schizophrenic subjects.|Association:Not Found|Conclusion:Our preliminary data suggest that mutation carriers might have an increased susceptibility to polydipsia through an undetermined mechanism. Our preliminary data suggest that mutation hcrtr1 might have an increased susceptibility to polydipsia through an undetermined mechanism Results support the hypothesis that the HCRTR1 Ile408Val polymorphism may confer susceptibility to polydipsia in schizophrenia |
Human | HCRT | 3060 | hypocretin (orexin) neuropeptide precursor | Title:Association of an orexin 1 receptor 408Val variant with polydipsia-hyponatremia in schizophrenic subjects.|Association:Not Found|Conclusion:Our preliminary data suggest that mutation carriers might have an increased susceptibility to polydipsia through an undetermined mechanism. |
Human | DRD2 | 1813 | dopamine receptor D2 | The present data suggests polymorphisms in DRD2 may confer susceptibility to polydipsia in schizophrenia |
Human | ACE | 1636 | angiotensin I converting enzyme | Title:Association of an orexin 1 receptor 408Val variant with polydipsia-hyponatremia in schizophrenic subjects.|Association:Y|Conclusion:Our preliminary data suggest that mutation carriers might have an increased susceptibility to polydipsia through an undetermined mechanism. the ACE D allele may be a risk factor for polydipsia/water intoxication in patients with schizophrenia |
Human | CTNS | 1497 | cystinosin, lysosomal cystine transporter | |
Human | CASR | 846 | calcium-sensing receptor | |
Human | AVPR2 | 554 | arginine vasopressin receptor 2 | |
Human | AQP2 | 359 | aquaporin 2 (collecting duct) | |