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Browse result for Nephronophthisis
※ introduction Nephronophthisis is a genetic disorder of the kidneys which affects children. It is classified as a medullary cystic kidney disease. The disorder is inherited in an autosomal recessive fashion and, although rare, is the most common genetic cause of childhood kidney failure. It is a form of ciliopathy. Its incidence has been estimated to be 0.9 cases per million people in the United States, and 1 in 50,000 births in Canada.
Reference
Wiki: Nephronophthisis
Reference
Wiki: Nephronophthisis
| PTMD ID | UniProt Accession | Entrez ID | Gene Name | Protein Name | Organism |
|---|---|---|---|---|---|
| PTMD00805 | Q9NQS7 | 3619 | INCENP | Inner centromere protein | Homo sapiens |
| PTMD02421 | O14745 | 9368 | NHERF1 | Na/H exchange regulatory cofactor NHE-RF1 /H exchanger) | Homo sapiens |
| PTMD02554 | O15259 | 4867 | NPHP1 | Nephrocystin-1 | Homo sapiens |
| PTMD02859 | O60336 | 23005 | MAPKBP1 | Mitogen-activated protein kinase-binding protein 1 | Homo sapiens |
| PTMD03027 | O75161 | 26173 | NPHP4 | Nephrocystin-4 | Homo sapiens |
| PTMD06892 | Q15051 | 9657 | IQCB1 | IQ calmodulin-binding motif-containing protein 1 | Homo sapiens |
| PTMD08005 | Q68DC2 | 20328 | ANKS6 | Ankyrin repeat and SAM domain-containing protein 6 | Homo sapiens |
| PTMD08826 | Q7Z494 | 27031 | NPHP3 | Nephrocystin-3 | Homo sapiens |
| PTMD10081 | Q8NEZ3 | 57728 | WDR19 | WD repeat-containing protein 19 | Homo sapiens |
| PTMD12402 | Q9BZE0 | 84662 | GLIS2 | Zinc finger protein GLIS2 | Homo sapiens |
| PTMD13292 | Q9NQH7 | 63929 | XPNPEP3 | Xaa-Pro aminopeptidase 3 | Homo sapiens |
| PTMD14555 | Q9UPV0 | 22897 | CEP164 | Centrosomal protein of 164 kDa | Homo sapiens |
| PTMD14626 | Q9Y283 | 27130 | INVS | Inversin | Homo sapiens |
