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ATRIP

Gene

ATR interacting protein

HGNCHGNC:33499EnsemblENSG00000164053NCBI Gene84126
Locus: gene with protein productLocation: 3p21.31

Also known as

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

Also known asFLJ12343 · MGC20625 · MGC21482 · MGC26740
View full nomenclature history (4)
Alias symbolsFLJ12343, MGC20625, MGC21482, MGC26740

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.

Lupus Erythematosus, Systemic
Microcephalic primordial dwarfism
Seckel syndrome
Genetic Diseases, Inborn
Neurodegenerative Diseases

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.

Armadillo like helical domain containing

Provenance

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