KCND3 gene

potassium voltage-gated channel subfamily D member 3

The information on this page was automatically extracted from online scientific databases.

From NCBI Gene:

Voltage-gated potassium (Kv) channels represent the most complex class of voltage-gated ion channels from both functional and structural standpoints. Their diverse functions include regulating neurotransmitter release, heart rate, insulin secretion, neuronal excitability, epithelial electrolyte transport, smooth muscle contraction, and cell volume. Four sequence-related potassium channel genes - shaker, shaw, shab, and shal - have been identified in Drosophila, and each has been shown to have human homolog(s). This gene encodes a member of the potassium channel, voltage-gated, shal-related subfamily, members of which form voltage-activated A-type potassium ion channels and are prominent in the repolarization phase of the action potential. This member includes two isoforms with different sizes, which are encoded by alternatively spliced transcript variants of this gene. [provided by RefSeq, Jul 2008]

From UniProt:

Pore-forming (alpha) subunit of voltage-gated rapidly inactivating A-type potassium channels. May contribute to I(To) current in heart and I(Sa) current in neurons. Channel properties are modulated by interactions with other alpha subunits and with regulatory subunits.

Covered on Genetics Home Reference:

From NCBI Gene:

  • Brugada syndrome 9
  • Spinocerebellar ataxia 19

From UniProt:

Spinocerebellar ataxia 19 (SCA19): A form of spinocerebellar ataxia, a clinically and genetically heterogeneous group of cerebellar disorders. Patients show progressive incoordination of gait and often poor coordination of hands, speech and eye movements, due to degeneration of the cerebellum with variable involvement of the brainstem and spinal cord. SCA19 is a relatively mild, cerebellar ataxic syndrome with cognitive impairment, pyramidal tract involvement, tremor and peripheral neuropathy, and mild atrophy of the cerebellar hemispheres and vermis. [MIM:607346]

Brugada syndrome 9 (BRGDA9): A tachyarrhythmia characterized by right bundle branch block and ST segment elevation on an electrocardiogram (ECG). It can cause the ventricles to beat so fast that the blood is prevented from circulating efficiently in the body. When this situation occurs, the individual will faint and may die in a few minutes if the heart is not reset. [MIM:616399]

Cytogenetic Location: 1p13.2, which is the short (p) arm of chromosome 1 at position 13.2

Molecular Location: base pairs 111,770,662 to 111,989,577 on chromosome 1 (Homo sapiens Annotation Release 108, GRCh38.p7) (NCBI)

Cytogenetic Location: 1p13.2, which is the short (p) arm of chromosome 1 at position 13.2
  • BRGDA9
  • KCND3L
  • KCND3S
  • KSHIVB
  • KV4.3
  • SCA19
  • SCA22