
KCNC1 - Wikipedia
Potassium voltage-gated channel subfamily C member 1 is a protein that in humans is encoded by the KCNC1 gene. [5][6][7] The Shaker gene family of Drosophila encodes components of …
KCNC1 Gene - GeneCards | KCNC1 Protein | KCNC1 Antibody
2024年12月25日 · KCNC1 (Potassium Voltage-Gated Channel Subfamily C Member 1) is a Protein Coding gene. Diseases associated with KCNC1 include Epilepsy, Progressive …
KCNC1-Related Disorders - Children's Hospital of Philadelphia
When a disorder is traced back to a disease-causing (pathogenic) variant in the KCNC1 gene, it is called a KCNC1 -related disorder. KCNC1 -related disorders fall into defined clinical categories …
3746 - Gene ResultKCNC1 potassium voltage-gated channel …
Gene ID: 3746, updated on 8-Feb-2025. This gene encodes a member of a family of integral membrane proteins that mediate the voltage-dependent potassium ion permeability of …
(PDF) Methylation gene KCNC1 is associated with overall survival in ...
2021年3月22日 · KCNC1 was identified as a DEG, in which hypermethylation inhibited its expression and it was associated with poor overall survival in patients with seminoma. The …
KCNC1 protein expression summary - The Human Protein Atlas
Specificity of RNA expression in 17 cancer types is categorized as either cancer enriched, group enriched, cancer enhanced, low cancer specificity and not detected. The RNA data was used …
KCNC1‐related disorders: new de novo variants expand the …
2019年6月7日 · We identified three new de novo missense variants in KCNC1 in five unrelated individuals causing different phenotypes featuring either isolated nonprogressive myoclonus …
KCNC1 - an overview | ScienceDirect Topics
KCNC1, also known as K V 3.1, is a type of potassium channel expressed in specific neurons involved in action potential propagation and synaptic transmission. Variants in KCNC1 have …
KCNC1-related disorders: new de novo variants expand the
A recurrent de novo missense variant in KCNC1, encoding a voltage-gated potassium channel expressed in inhibitory neurons, causes progressive myoclonus epilepsy and ataxia, and a …
KCNC1 Foundation
Our mission, our fight for a brighter future is won when there is a cure for our babies suffering from KCNC1-related disorders. This will be accomplished through supporting research to …