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PALS1

Gene

protein associated with LIN7 1, MAGUK p55 family member

HGNCHGNC:18669EnsemblENSG00000072415NCBI Gene64398
Locus: gene with protein productLocation: 14q23.3

Also known as

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

Also known asMPP5 · FLJ12615
View full nomenclature history (7)
Previous symbolsMPP5
Alias symbolsFLJ12615
Previous namesmembrane protein, palmitoylated 5 (MAGUK p55 subfamily member 5), membrane palmitoylated protein 5, protein associated with LIN7 1, MAGUK family member
Alias namesstardust, protein associated with Lin-7 1

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.

COVID-19
Severe Acute Respiratory Syndrome
Complex neurodevelopmental disorder
Cerebral Palsy

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.

Gene family

HGNC gene-group membership.

Membrane associated guanylate kinasesPDZ domain containingCrumbs complex components

Provenance

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