PGAP1

Gene

post-GPI attachment to proteins inositol deacylase 1

HGNCHGNC:25712 EnsemblENSG00000197121 NCBI Gene80055

Locus: gene with protein productLocation: 2q33.1

Also known as

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

Also known asFLJ12377 · Bst1 · SPG67

View full nomenclature history (5)

Alias symbolsFLJ12377, Bst1, SPG67

Previous namespost-GPI attachment to proteins 1

Alias namesGPI inositol-deacylase

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.

Autosomal recessive non-syndromic intellectual disability

Genetic Diseases, Inborn

Spastic Paraplegia, Hereditary

Thyroid Neoplasms

Neurodevelopmental Disorders

Alcohol drinking

Myopia

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.