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ALPI

Gene

alkaline phosphatase, intestinal

HGNCHGNC:437EnsemblENSG00000163295NCBI Gene248
Locus: gene with protein productLocation: 2q37.1

Also known as

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

Also known asIAP
View full nomenclature history (2)
Alias symbolsIAP
Alias namesintestinal alkaline phosphatase

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.

Inflammatory Bowel Diseases
Neurodegenerative Diseases
Urolithiasis
Autoimmune disorder of central nervous system
Diabetes Mellitus, Type 2

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.

Alkaline phosphatases

Provenance

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