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TPTE2

Gene

transmembrane phosphoinositide 3-phosphatase and tensin homolog 2

HGNCHGNC:17299EnsemblENSG00000132958NCBI Gene93492
Locus: gene with protein productLocation: 13q12.11

Also known as

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

Also known asTPIP
View full nomenclature history (1)
Alias symbolsTPIP

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.

immunoglobulin G4-related sclerosing disease
Chronic Kidney Disease-Mineral and Bone Disorder
Muscular Atrophy
Spermatogenic failure
Non-syndromic male infertility due to sperm motility disorder

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.

C2 tensin-type domain containingPTEN protein phosphatases

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-03-15.
Open TargetsGene–disease associations from the Open Targets Platform.