Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
3790
Gene name Gene Name - the full gene name approved by the HGNC.
Potassium voltage-gated channel modifier subfamily S member 3
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
KCNS3
Synonyms (NCBI Gene) Gene synonyms aliases
KV9.3
Chromosome Chromosome number
2
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
2p24.2
Summary Summary of gene provided in NCBI Entrez Gene.
Voltage-gated potassium channels form the largest and most diversified class of ion channels and are present in both excitable and nonexcitable cells. Their main functions are associated with the regulation of the resting membrane potential and the contro
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT005009 hsa-miR-125b-5p Microarray 17891175
MIRT022698 hsa-miR-124-3p Microarray 18668037
MIRT024380 hsa-miR-215-5p Microarray 19074876
MIRT026551 hsa-miR-192-5p Microarray 19074876
MIRT1082462 hsa-miR-192 CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005249 Function Voltage-gated potassium channel activity IBA 21873635
GO:0005251 Function Delayed rectifier potassium channel activity TAS 10484328
GO:0005794 Component Golgi apparatus IDA
GO:0005829 Component Cytosol IDA
GO:0005886 Component Plasma membrane IDA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
603888 6302 ENSG00000170745
Protein
UniProt ID Q9BQ31
Protein name Delayed-rectifier potassium channel regulatory subunit KCNS3 (Delayed-rectifier K(+) channel alpha subunit 3) (Delayed-rectifier potassium channel subunit Kv9.3) (Kv9.3) (Potassium voltage-gated channel subfamily S member 3)
Protein function Potassium channel regulatory subunit that modulates the delayed rectifier potassium channel activity of KCNB1 by namely slowing down the deactivation and inactivation time constants (PubMed:10484328). While it does not form functional channel on
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF02214 BTB_2 17 116 BTB/POZ domain Domain
PF00520 Ion_trans 184 417 Ion transport protein Family
Tissue specificity TISSUE SPECIFICITY: Detected in whole normal term placental and placental chorionic plate arteries and veins. Detected in syncytiotrophoblast and in blood vessel endothelium within intermediate villi and chorionic plate (at protein level) (PubMed:22943705
Sequence
Sequence length 491
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 information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Schizophrenia Schizophrenia rs13447324, rs387906932, rs387906933, rs863223354, rs863223355, rs776061422, rs863223349, rs748809996, rs759748655, rs863223353, rs863223350, rs863223356, rs781821239, rs863223348, rs863223346
View all (12 more)
24170294
Unknown
Disease term Disease name Evidence References Source
Coenzyme Q10 Deficiency Coenzyme Q10 Deficiency GWAS
Amyotrophic Lateral Sclerosis Amyotrophic Lateral Sclerosis GWAS
Gout Gout GWAS
Diabetes Diabetes GWAS
Associations from Text Mining
Disease Name Relationship Type References
Lung Diseases Associate 26635082
Pulmonary Arterial Hypertension Associate 34349187