Keyword Analysis & Research: kcnc2

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Keyword CPC PCC Volume Score Length of keyword
kcnc21.610.95680485

Keyword Research: People who searched kcnc2 also searched

Keyword CPC PCC Volume Score
kcnc21.920.7827486
kcnc2 antibody1.460.574323
kcnc2 gene1.030.694647
kcnc2 protein1.20.5880659
kcc2 antibody0.090.2115581

Search Results related to kcnc2 on Search Engine

  • KCNC2 - Wikipedia

    wikipedia.org

    https://en.wikipedia.org/wiki/KCNC2

    WebPotassium voltage-gated channel subfamily C member 2 is a protein that in humans is encoded by the KCNC2 gene. The protein encoded by this gene is a voltage-gated potassium channel subunit (Kv3.2).

    DA: 91 PA: 22 MOZ Rank: 100

  • KCNC2 Gene - GeneCards | KCNC2 Protein | KCNC2 Antibody

    genecards.org

    https://www.genecards.org/cgi-bin/carddisp.pl?gene=KCNC2

    WebApr 3, 2024 · KCNC2 (Potassium Voltage-Gated Channel Subfamily C Member 2) is a Protein Coding gene. Diseases associated with KCNC2 include Developmental And Epileptic Encephalopathy 103 and Developmental And Epileptic Encephalopathy. Among its related pathways are Integration of energy metabolism and Potassium Channels.

    DA: 35 PA: 69 MOZ Rank: 45

  • KCNC2 potassium voltage-gated channel subfamily C member 2

    nih.gov

    https://www.ncbi.nlm.nih.gov/gene/3747

    WebKCNC2 potassium voltage-gated channel subfamily C member 2 [ (human)] Gene ID: 3747, updated on 23-Nov-2023. Summary. The Shaker gene family of Drosophila encodes components of voltage-gated potassium channels and is comprised of four subfamilies.

    DA: 75 PA: 71 MOZ Rank: 65

  • KCNC2 potassium voltage-gated channel subfamily C member 2

    nih.gov

    https://www.ncbi.nlm.nih.gov/gtr/genes/3747/

    WebNov 23, 2023 · KCNC2. potassium voltage-gated channel subfamily C member 2. Gene ID: 3747, updated on 23-Nov-2023. Gene type: protein coding. Also known as: KV3.2; DEE103. See all available tests in GTR for this gene. Go to complete Gene record for KCNC2. Go to Variation Viewer for KCNC2 variants.

    DA: 93 PA: 77 MOZ Rank: 15

  • KCNC2 – a novel epilepsy gene harbors an unusual phenotypic …

    epilepsygenetics.net

    http://epilepsygenetics.net/2022/04/26/kcnc2-a-novel-epilepsy-gene-harbors-an-unusual-phenotypic-spectrum/

    WebApr 26, 2022 · KCNC2 is a new epilepsy gene, a new epilepsy-related potassium channelopathy. With a phenotypic spectrum of de novo variants emerging that span the DEEs, there is an unusual preponderance of generalized DEEs including early-onset absence epilepsies and myoclonic-astatic epilepsy.

    DA: 70 PA: 37 MOZ Rank: 68

  • Spectrum of Phenotypic, Genetic, and Functional ... - PubMed

    nih.gov

    https://pubmed.ncbi.nlm.nih.gov/35314505/

    WebMar 22, 2022 · These findings implicate KCNC2 as a novel causative gene for epilepsy and emphasize the critical role of K V 3.2 in the regulation of brain excitability. Spectrum of Phenotypic, Genetic, and Functional Characteristics in Patients With Epilepsy With KCNC2 Pathogenic Variants

    DA: 84 PA: 9 MOZ Rank: 27

  • Kcnc2 potassium voltage gated channel, Shaw-related subfamily, member …

    nih.gov

    https://www.ncbi.nlm.nih.gov/gene/268345

    WebFeb 8, 2024 · Kcnc2 potassium voltage gated channel, Shaw-related subfamily, member 2 [ (house mouse)] Gene ID: 268345, updated on 8-Feb-2024. Summary. Enables transmembrane transporter binding activity. Acts upstream of or within action potential. Located in several cellular components, including neuronal cell body membrane; …

    DA: 50 PA: 10 MOZ Rank: 2

  • Heterozygous variants in KCNC2 cause a broad spectrum of

    medrxiv.org

    https://www.medrxiv.org/content/10.1101/2021.05.21.21257099v1

    WebMay 23, 2021 · Conclusion These findings implicate KCNC2 as a novel causative gene for epilepsy emphasizing the critical role of KV3.2 in the regulation of brain excitability with an interesting genotype-phenotype correlation and a potential concept for precision medicine.

    DA: 11 PA: 93 MOZ Rank: 73

  • KCNC2 variants of uncertain significance are also associated

    nih.gov

    https://pubmed.ncbi.nlm.nih.gov/37360341/

    WebJun 9, 2023 · Recently, de novo variants in KCNC2, coding for the potassium channel subunit K V 3.2, have been described as causative for various forms of epilepsy including genetic generalized epilepsy (GGE) and developmental and epileptic encephalopathy (DEE).

    DA: 35 PA: 50 MOZ Rank: 67

  • Investigation of novel de novo KCNC2 variants causing severe

    nih.gov

    https://pubmed.ncbi.nlm.nih.gov/36087422/

    WebPMID: 36087422. DOI: 10.1016/j.seizure.2022.09.004. Abstract. Purpose The voltage-gated potassium channel K v 3.2, encoded by KCNC2, facilitates fast-spiking GABAergic interneurons to fire action potentials at high frequencies. It is pivotal to maintaining excitation/inhibition balance in mammalian brains.

    DA: 15 PA: 2 MOZ Rank: 63