KCNT1 wt Allele

Preferred Label : KCNT1 wt Allele;

NCIt synonyms : KCa4.1; SLACK; bA100C15.2; Sequence Like A Calcium-Activated K Channel Gene; Slo2.2; KIAA1422; ENFL5; DEE14; EIEE14; Potassium Sodium-Activated Channel Subfamily T Member 1 wt Allele; Potassium Channel, Sodium Activated Subfamily T, Member 1 Gene; Potassium Channel, Subfamily T, Member 1 Gene;

NCIt definition : Human KCNT1 wild-type allele is located in the vicinity of 9q34.3 and is approximately 93 kb in length. This allele, which encodes potassium channel subfamily T member 1 protein, is involved in ion conductance and developmental signaling. Mutation of the gene is associated with developmental and epileptic encephalopathy 14 and nocturnal frontal lobe epilepsy 5.;

NCI Metathesaurus CUI : CL1799301;

GenBank Accession Number : AB037843;

Details

Origin ID

C190836;

UMLS CUI

C5781217;

OMIM relation
- Potassium channel, subfamily t, member 1 [OMIM gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
gene_found_in_organism
- Human [NCIt concept]
gene_in_chromosomal_location
- 9q34.3 [NCIt concept]
gene_plays_role_in_process
- G Protein-Coupled Receptor Signaling [NCIt concept]
- Ion Transport Process [NCIt concept]
- Ligand Binding [NCIt concept]
- Potassium Channel Binding [NCIt concept]
- Transmembrane Transport [NCIt concept]
- Transport Process [NCIt concept]

Keyword's position in hierarchy(ies) :

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