Gene Gene information from NCBI Gene database.
Entrez ID 3747
Gene name Potassium voltage-gated channel subfamily C member 2
Gene symbol KCNC2
Synonyms (NCBI Gene)
DEE103KV3.2
Chromosome 12
Chromosome location 12q21.1
Summary The Shaker gene family of Drosophila encodes components of voltage-gated potassium channels and is comprised of four subfamilies. Based on sequence similarity, this gene is similar to one of these subfamilies, namely the Shaw subfamily. The protein encode
miRNA miRNA information provided by mirtarbase database.
36
miRTarBase ID miRNA Experiments Reference
MIRT1080551 hsa-miR-1323 CLIP-seq
MIRT1080552 hsa-miR-214 CLIP-seq
MIRT1080553 hsa-miR-296-5p CLIP-seq
MIRT1080554 hsa-miR-299-3p CLIP-seq
MIRT1080555 hsa-miR-3619-5p CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
90
GO ID Ontology Definition Evidence Reference
GO:0001508 Process Action potential IBA
GO:0001508 Process Action potential IEA
GO:0005216 Function Monoatomic ion channel activity IEA
GO:0005249 Function Voltage-gated potassium channel activity IDA 15709110, 32392612, 36090251
GO:0005249 Function Voltage-gated potassium channel activity IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
176256 6234 ENSG00000166006
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q96PR1
Protein name Voltage-gated potassium channel KCNC2 (Potassium voltage-gated channel subfamily C member 2) (Shaw-like potassium channel) (Voltage-gated potassium channel Kv3.2)
Protein function Voltage-gated potassium channel that mediates transmembrane potassium transport in excitable membranes, primarily in the brain. Contributes to the regulation of the fast action potential repolarization and in sustained high-frequency firing in n
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF02214 BTB_2 10 151 BTB/POZ domain Domain
PF00520 Ion_trans 228 484 Ion transport protein Family
Sequence
Sequence length 638
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Voltage gated Potassium channels
Glucagon-like Peptide-1 (GLP1) regulates insulin secretion
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
15
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession Evidence Score
Developmental and epileptic encephalopathy Likely pathogenic rs2136944093 RCV002266114
★★★★☆
ClinVar: Pathogenic / Likely Pathogenic (<5 Variants)
Developmental and epileptic encephalopathy 103 Pathogenic; Likely pathogenic rs2136944684, rs2136943353, rs2137827783, rs61735712, rs2137828445, rs2136943757, rs2547844200, rs2548168192, rs1260222970 RCV002269377
RCV002260879
RCV002260880
RCV002260881
RCV002260882
View all (4 more)
★★★★★
ClinVar: Pathogenic / Likely Pathogenic (≥5 Variants)
Neurodevelopmental delay Likely pathogenic rs1881066035 RCV002274413
★★★★☆
ClinVar: Pathogenic / Likely Pathogenic (<5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
ATTENTION DEFICIT HYPERACTIVITY DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
EARLY INFANTILE EPILEPTIC ENCEPHALOPATHY WITH SUPPRESSION BURSTS Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
GENETIC DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
KCNC2-related disorder Uncertain significance ClinVar
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Autistic Disorder Autism Pubtator 35366058 Associate
★☆☆☆☆
Found in Text Mining only
Diabetes Diabetes BEFREE 27623749
★☆☆☆☆
Found in Text Mining only
Diabetes Mellitus Diabetes Mellitus BEFREE 27623749
★☆☆☆☆
Found in Text Mining only
Epilepsies Partial Partial epilepsy Pubtator 35314505 Associate
★☆☆☆☆
Found in Text Mining only
Epilepsy Epilepsy Pubtator 35314505, 35366058 Associate
★☆☆☆☆
Found in Text Mining only
Epilepsy Absence Absence epilepsy Pubtator 35314505 Associate
★☆☆☆☆
Found in Text Mining only
Epilepsy Generalized Generalized epilepsy Pubtator 35314505 Associate
★☆☆☆☆
Found in Text Mining only
Epileptic Encephalopathy Early Infantile 3 Developmental and epileptic encephalopathy Pubtator 35314505 Associate
★☆☆☆☆
Found in Text Mining only
Episodic Ataxia Episodic ataxia Pubtator 30314295 Associate
★☆☆☆☆
Found in Text Mining only
Episodic Ataxia Type 2 Episodic ataxia Pubtator 30314295 Associate
★☆☆☆☆
Found in Text Mining only