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KCNK9

potassium two pore domain channel subfamily K member 9

HCNC Approved Symbol
KCNK9 (HGNC:6283)
Genomic Coordinates
8:139,600,838 - 139,703,123 (8q24.3)
Synonyms
K2p9.1, TASK3, TASK-3
Disease Associations
This gene is associated with the following 1 diseases in OMIM.

Diagnosed Cases

2Patients

In total, 2 patients were diagnosed with a variant in the KCNK9 gene.

Frequently observed phenotypes

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

Cleft palate
 1 (50.0%)
Downturned mouth
 1 (50.0%)
Facial dysmorphism
 1 (50.0%)
Generalized hypotonia
 1 (50.0%)
Narrow bitemporal width
 1 (50.0%)
KCNK9 - Gene browser | 3billion