The KCNT1 gene homepage

General information
Gene symbol KCNT1
Gene name potassium channel, subfamily T, member 1
Chromosome 9
Chromosomal band q34.3
Imprinted Unknown
Genomic reference NG_033070.1
Transcript reference NM_020822.2
Exon/intron information NM_020822.2 exon/intron table
Associated with diseases EIEE14, ENFL5, ID
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 308
Unique public DNA variants reported 238
Individuals with public variants 45
Hidden variants 29
Date created May 03, 2013
Date last updated October 23, 2023
Version KCNT1:231023

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
Reading frame checker The Reading-frame checker generates a prediction of the effect of whole-exon changes. Active for: NM_020822.2.
UCSC Genome Browser Show variants in the UCSC Genome Browser (full view, compact view)
Ensembl Genome Browser Show variants in the Ensembl Genome Browser (full view, compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer

Links to other resources
HGNC 18865
Entrez Gene 57582
PubMed articles KCNT1
OMIM - Gene 608167
OMIM - Diseases EIEE14 (encephalopathy, epileptic, early infantile, type 14 (EIEE-14))
ENFL5 (epilepsy, frontal lobe, nocturnal, type 5 (ENFL-5))
Orphanet KCNT1

Active transcripts




NCBI ID     

NCBI Protein ID     

00010424 9 potassium channel, subfamily T, member 1 NM_020822.2 NP_065873.2 308

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