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ALPI

Chr 2q37.1

alkaline phosphatase, intestinal

Aliases:
IAP
MANE:
ENST00000295463.4

Annotations refreshed 1 month ago.

Predicted protein structure

Clinical relevance (Genomics England PanelApp)

Diagnostic Grade (Green)

  • COVID-19 research

    BIALLELIC, autosomal or pseudoautosomal
  • Primary immunodeficiency or monogenic inflammatory bowel disease

    BIALLELIC, autosomal or pseudoautosomal

Disease associations (Open Targets)

  • inflammatory bowel disease

    0.50
  • neurodegenerative disease

    0.36
  • vertebral column disorder

    0.28
  • urolithiasis

    0.27
  • response to antibiotic

    0.23
  • autoimmune disorder of central nervous system

    0.22
  • chronic primary adrenal insufficiency

    0.14
  • familial glucocorticoid deficiency

    0.14
  • Progressive visual loss

    0.10
  • type 2 diabetes mellitus

    0.08

Score is the Open Targets composite evidence score (0-1). Higher = stronger gene-disease association.

Protein function (UniProt)

Intestinal-type alkaline phosphatase

Alkaline phosphatase that can hydrolyze various phosphate compounds

Curated MONDO disease pages that list ALPI among their top associated genes.

Data sources: HGNC (CC BY 4.0), AlphaFold (CC BY 4.0, Jumper et al. Nature 2021), Genomics England PanelApp (CC BY 4.0), ClinGen, Open Targets (CC0), UniProt.

Not for sole clinical decision-making. Always verify against primary sources.