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IFITM5

Gene

interferon induced transmembrane protein 5

HGNCHGNC:16644EnsemblENSG00000206013NCBI Gene387733
Locus: gene with protein productLocation: 11p15.5

Also known as

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

Also known asBRIL · Hrmp1 · fragilis4 · DSPA1
View full nomenclature history (5)
Alias symbolsBRIL, Hrmp1, fragilis4, DSPA1
Alias namesdispanin subfamily A member 1

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.

Osteogenesis Imperfecta
Osteoporosis, Postmenopausal
Genetic Diseases, Inborn
Hypocalcemic vitamin D-resistant rickets
Metaphyseal anadysplasia

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.

Interferon induced transmembrane protein familyDispanins

Provenance

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