eDiPNet

Subtype of: Polycystic kidney disease

Show by gene (one row per gene, with all of its disease terms together)

Pathways column key: KEGG Reactome

Disease Term	Disease ID	Gene Symbol	Classification	References	Source	Pathways
ALG9-associated autosomal dominant polycystic kidney disease	MONDO:0700000	ALG9	Causal	—	ClinGen	N-Glycan biosynthesis Various types of N-glycan biosynthesis Metabolic pathways +2 more
autosomal dominant polycystic kidney disease	730 MONDO:0004691 MONDO_0004691	DNAJB11	Causal	—	ClinGen	Protein processing in endoplasmic reticulum XBP1(S) activates chaperone genes
		IFT140	Causal	—	ClinGen	Hedgehog 'off' state Intraflagellar transport
		PKD1	Causal	19165178 20558538 22034641 23624871 28378423	ClinGen, Open Targets	VxPx cargo-targeting to cilium
		PKD2	Causal	28356211 23431072	ClinGen, Open Targets	VxPx cargo-targeting to cilium
		ALG5	Unknown	—	ClinGen	N-Glycan biosynthesis Metabolic pathways Synthesis of dolichyl-phosphate-glucose
		ALG8	Unknown	—	ClinGen	N-Glycan biosynthesis Metabolic pathways Biosynthesis of the N-glycan precursor (dolichol lipid-linked oligosaccharide, LLO) and transfer to a nascent protein +1 more
		ALG9	Unknown	31395617	Open Targets	N-Glycan biosynthesis Various types of N-glycan biosynthesis Metabolic pathways +2 more
		NEK8	Unknown	—	ClinGen	—

Autosomal dominant polycystic kidney disease