KCND3

Gene

1 paper1 finding

  • 1 lab in 1 country
  • Funders: National Science and Technology Council and 1 more
  • Animals1

Associations

1

Spinocerebellar ataxia

upin mice1

1 study
  1. KCND3 is associated with spinocerebellar ataxia in mice.

    “Kcnd3 F227del mutation may not only result in a loss of function but also act as a dominant, toxic gain-of-function variant associated with both ataxia and memory impairments”

    Animalsknock-in mutation

    Dietary restriction mitigates cognitive impairments in a mouse model of SCA19/22

    Mechanisms of ageing and development17 Jan 2026

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