Disease-gene associations mined from literature

Literature associating KCNN3 and autosomal dominant dyskeratosis congenita 3

KCNN3 [ENSP00000481848]

Potassium intermediate/small conductance calcium-activated channel, subfamily N, member 3; Forms a voltage-independent potassium channel activated by intracellular calcium. Activation is followed by membrane hyperpolarization. Thought to regulate neuronal excitability by contributing to the slow component of synaptic afterhyperpolarization. The channel is blocked by apamin; Potassium calcium-activated channels

Synonyms:  KCNN3,  KCNN3p,  hKCNN3,  Q6JXY2,  Q9UGI6 ...

Linkouts:  STRING  Pharos  UniProt