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 …

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 …

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 …

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 …

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 …

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 …

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, 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 …

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 …

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 …