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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



PTMD IDUniProt AccessionEntrez IDGene NameProtein NameOrganism
PTMD00805Q9NQS73619
INCENP
Inner centromere protein
Homo sapiens
PTMD02421O147459368
NHERF1
Na/H exchange regulatory cofactor NHE-RF1 /H exchanger)
Homo sapiens
PTMD02554O152594867
NPHP1
Nephrocystin-1
Homo sapiens
PTMD02859O6033623005
MAPKBP1
Mitogen-activated protein kinase-binding protein 1
Homo sapiens
PTMD03027O7516126173
NPHP4
Nephrocystin-4
Homo sapiens
PTMD06892Q150519657
IQCB1
IQ calmodulin-binding motif-containing protein 1
Homo sapiens
PTMD08005Q68DC220328
ANKS6
Ankyrin repeat and SAM domain-containing protein 6
Homo sapiens
PTMD08826Q7Z49427031
NPHP3
Nephrocystin-3
Homo sapiens
PTMD10081Q8NEZ357728
WDR19
WD repeat-containing protein 19
Homo sapiens
PTMD12402Q9BZE084662
GLIS2
Zinc finger protein GLIS2
Homo sapiens
PTMD13292Q9NQH763929
XPNPEP3
Xaa-Pro aminopeptidase 3
Homo sapiens
PTMD14555Q9UPV022897
CEP164
Centrosomal protein of 164 kDa
Homo sapiens
PTMD14626Q9Y28327130
INVS
Inversin
Homo sapiens