nephrogenic diabetes insipidus Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An impaired renal function disease characterized by a complete or partial resistance of the kidneys to vasopressin (ADH). (Human Disease Ontology, DOID_12387)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0009806
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Genes

20 genes associated with the nephrogenic diabetes insipidus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AQP2 aquaporin 2 (collecting duct)
ARL6 ADP-ribosylation factor-like 6
BBS1 Bardet-Biedl syndrome 1
BBS10 Bardet-Biedl syndrome 10
BBS12 Bardet-Biedl syndrome 12
BBS2 Bardet-Biedl syndrome 2
BBS4 Bardet-Biedl syndrome 4
BBS5 Bardet-Biedl syndrome 5
BBS7 Bardet-Biedl syndrome 7
BBS9 Bardet-Biedl syndrome 9
CEP290 centrosomal protein 290kDa
IFT27 intraflagellar transport 27
LZTFL1 leucine zipper transcription factor-like 1
MKKS McKusick-Kaufman syndrome
MKS1 Meckel syndrome, type 1
TRIM32 tripartite motif containing 32
TTC8 tetratricopeptide repeat domain 8
VIPAS39 VPS33B interacting protein, apical-basolateral polarity regulator, spe-39 homolog
VPS33B vacuolar protein sorting 33 homolog B (yeast)
WDPCP WD repeat containing planar cell polarity effector