Alternating Hemiplegia and Hemiplegic Migraine
Gene: KCNK18

KCNK18 (potassium two pore domain channel subfamily K member 18)
EnsemblGeneIds (GRCh38): ENSG00000186795
EnsemblGeneIds (GRCh37): ENSG00000186795
OMIM: 613655, Gene2Phenotype
KCNK18 is in 2 panels

1 review

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Green List (high evidence)

Case level and functional data support association, gene also known as TRESK.
Created: 8 Oct 2020, 10:30 a.m. | Last Modified: 8 Oct 2020, 10:30 a.m.

Panel Version: 0.28

Mode of inheritance
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted

Phenotypes
{Migraine, with or without aura, susceptibility to, 13}, MIM# 613656

Publications

Created: 8 Oct 2020, 10:30 a.m.
Last Modified: 8 Oct 2020, 10:30 a.m.
Panel version: 0.28

Details

Mode of Inheritance

MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted

Sources

Expert Review Green
Victorian Clinical Genetics Services

Phenotypes

{Migraine, with or without aura, susceptibility to, 13}, MIM# 613656

OMIM

613655

Clinvar variants

Variants in KCNK18

Penetrance

None

Publications

Panels with this gene