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Everything about KCNN2
Protein-coding gene in the species Homo sapiens
Potassium intermediate/small conductance calcium-activated channel, subfamily N, member 2, also known as KCNN2, is a protein which in humans is encoded by the KCNN2 gene. KCNN2 is an ion channel protein also known as KCa2.2. Wikipedia →
🧭 Start here: a 6-step reading path
- Read the overview: KCNN2A 5-minute orientation
- Skim a recent paper: A Novel KCNN2 Variant in a Family with Essential Tremor Plus: Clinical Characteristics and In Silico AnalysisInfluential work since 2022
- Read the landmark paper: Variants in the SK2 channel gene (KCNN2) lead to dominant neurodevelopmental movement disordersCited 53 times
- Go sideways: KCNN1A closely related topic
- Go sideways: KCNN3A closely related topic
📖 Definitions
No dictionary entry for this exact phrase.
🗂️ The subject at a glance
🏆 Landmark papers (most cited)
Variants in the SK2 channel gene (KCNN2) lead to dominant neurodevelopmental movement disorders
KCNN2 mutation in autosomal‐dominant tremulous myoclonus‐dystonia
Kcnn2 blockade reverses learning deficits in a mouse model of fetal alcohol spectrum disorders
Identification of KCNN2 as a susceptibility locus for coronary artery aneurysms in Kawasaki disease using genome-wide association analysis
Behavioral effects of a deletion in Kcnn2, the gene encoding the SK2 subunit of small-conductance Ca2+-activated K+ channels
HDAC2-dependent remodeling of KCa2.2 (KCNN2) and KCa2.3 (KCNN3) K+ channels in atrial fibrillation with concomitant heart failure
Assessment of mutations in KCNN2 and ZNF135 to patient neurological symptoms
KCNN2 polymorphisms and cardiac tachyarrhythmias
🆕 Influential since 2022
A Novel KCNN2 Variant in a Family with Essential Tremor Plus: Clinical Characteristics and In Silico Analysis
K Ca 2 .2 ( KCNN2 ): A physiologically and therapeutically important potassium channel
KCNN2 Mutation in Pediatric Tremor Myoclonus Dystonia Syndrome with Electrophysiological Evaluation
Insufficient effect of deep brain stimulation in a patient with KCNN2-associated myoclonus-dystonia
Early‐Onset Neurodevelopmental Movement Disorder Secondary to Novel Mutation in KCNN2
📚 Books worth reading
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🔗 Related topics
- KCNN1 Potassium intermediate/small conductance calcium-activated channel, subfamily N, member 1 , also known as KCNN1, is a human gene encoding the KCa2.1 protein…
- KCNN3 SK3 (small conductance calcium-activated potassium channel 3) also known as KCa2.3 is a protein that in humans is encoded by the KCNN3 gene. SK3 is a small-cond…
- SK channel SK channels (small conductance calcium-activated potassium channels) are a subfamily of calcium-activated potassium channels. They are so called because…
- KCNN4 Potassium intermediate/small conductance calcium-activated channel, subfamily N, member 4, also known as KCNN4, is a human gene encoding the KCa3.1 protein…
- KCNMA1 Calcium-activated potassium channel subunit alpha-1 also known as large conductance calcium-activated potassium channel, subfamily M, alpha member 1 (KCa1…
- KCNT1 Potassium channel subfamily T, member 1, also known as KCNT1 or SLACK, is a human gene that encodes the KCa4.1 protein. KCa4.1 is a member of the calcium-activa…
- Calcium-activated potassium channel Calcium-activated potassium channels are potassium channels gated by calcium, or that are structurally or phylogenetically related to calcium gated channels…
- KCNU1 Potassium channel, subfamily U, member 1, also known as KCNU1, is a gene encoding the KCa5.1 protein. Although this channel is structurally related to…