stage 5 chronic kidney disease Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link
Similar Terms
Downloads & Tools


37 genes associated with the stage 5 chronic kidney disease phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ADCK4 aarF domain containing kinase 4
AHI1 Abelson helper integration site 1
CD151 CD151 molecule (Raph blood group)
CEP290 centrosomal protein 290kDa
CEP83 centrosomal protein 83kDa
CFHR5 complement factor H-related 5
COL4A3 collagen, type IV, alpha 3 (Goodpasture antigen)
COL4A4 collagen, type IV, alpha 4
COL4A5 collagen, type IV, alpha 5
CTNS cystinosin, lysosomal cystine transporter
DGKE diacylglycerol kinase, epsilon 64kDa
FAN1 FANCD2/FANCI-associated nuclease 1
FN1 fibronectin 1
GLIS2 GLIS family zinc finger 2
HNF1B HNF1 homeobox B
IFT140 intraflagellar transport 140
IFT43 intraflagellar transport 43
INF2 inverted formin, FH2 and WH2 domain containing
INVS inversin
IQCB1 IQ motif containing B1
LAMB2 laminin, beta 2 (laminin S)
MUC1 mucin 1, cell surface associated
MUT methylmalonyl CoA mutase
MYH9 myosin, heavy chain 9, non-muscle
NEK8 NIMA-related kinase 8
NPHP1 nephronophthisis 1 (juvenile)
NPHP4 nephronophthisis 4
NPHS2 nephrosis 2, idiopathic, steroid-resistant (podocin)
PAX2 paired box 2
PLCE1 phospholipase C, epsilon 1
RAD51C RAD51 paralog C
SLC7A7 solute carrier family 7 (amino acid transporter light chain, y+L system), member 7
TMEM67 transmembrane protein 67
TTC21B tetratricopeptide repeat domain 21B
WDR19 WD repeat domain 19
WT1 Wilms tumor 1
XPNPEP3 X-prolyl aminopeptidase 3, mitochondrial