Back to discover

KIDINS220

Gene

kinase D interacting substrate 220

HGNCHGNC:29508EnsemblENSG00000134313NCBI Gene57498
Locus: gene with protein productLocation: 2p25.1

Also known as

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

Also known asARMS
View full nomenclature history (3)
Alias symbolsARMS
Previous nameskinase D-interacting substrate 220kDa
Alias namesankyrin repeat-rich membrane-spanning protein

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.

Neurodegenerative Diseases
Genetic Diseases, Inborn
Autoimmune disorder of central nervous system
Spastic Paraplegia, Hereditary
Cerebral Palsy

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.

Ankyrin repeat domain containing

Provenance

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