KCNT1 - Gene browser

KCNT1

potassium sodium-activated channel subfamily T member 1

HCNC Approved Symbol: KCNT1 (HGNC:18865)
Genomic Coordinates: 9:135,702,185 - 135,795,502 (9q34.3)
Synonyms: KCa4.1, KIAA1422, SLACK, Slo2.2
Disease Associations: This gene is associated with the following 2 diseases in OMIM.

14Patients

In total, 14 patients were diagnosed with a variant in the KCNT1 gene.

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

014
Patient count

Epilepsy: 5 (35.7%)
Patient Count: 5 (35.7%)
% of total patients presenting each phenotype is shown in parentheses.
5 (35.7%)
Seizures: 5 (35.7%)
Patient Count: 5 (35.7%)
% of total patients presenting each phenotype is shown in parentheses.
5 (35.7%)
Global developmental delay: 3 (21.4%)
Patient Count: 3 (21.4%)
% of total patients presenting each phenotype is shown in parentheses.
3 (21.4%)
Microcephaly: 2 (14.3%)
Patient Count: 2 (14.3%)
% of total patients presenting each phenotype is shown in parentheses.
2 (14.3%)
Swallowing difficulties: 2 (14.3%)
Patient Count: 2 (14.3%)
% of total patients presenting each phenotype is shown in parentheses.
2 (14.3%)