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PKD1L1

Gene

polycystin 1 like 1, transient receptor potential channel interacting

HGNCHGNC:18053EnsemblENSG00000158683NCBI Gene168507
Locus: gene with protein productLocation: 7p12.3

Also known as

Symbols and names change; identity (the HGNC ID) does not. Previous and alternative forms are kept distinct.

Also known asPRO19563
View full nomenclature history (3)
Alias symbolsPRO19563
Previous namespolycystic kidney disease 1 like 1
Alias namespolycystin-1L1

Associated diseases

via associated_with

Diseases linked to this gene through the canonical GENE→DISEASE (associated_with) relation, drawn from Open Targets' top-ranked associations by overall score — not the full association set. Disease-level detail lives on each disease's own page.

Heterotaxia
Visceral heterotaxy
Genetic Diseases, Inborn
Neurotoxicity Syndromes
Idiopathic Pulmonary Fibrosis
Glomerulonephritis, IGA

Drawn from Open Targets’ top 10 associations by overall score for this gene — the subset resolved to a canonical disease. Lower-ranked associations, and diseases not yet canonicalised, are not shown.

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-01-20.
Open TargetsGene–disease associations from the Open Targets Platform.