ATP1A2

ATPase Na+/K+ transporting subunit alpha 2
OMIM: 182340
PanelMode of inheritanceDetails
6 panels
R-numbers: R56
Signed-off version 1.121
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
familial basilar migraine OMIM:602481, familial hemiplegic migraine type 2 OMIM:602481, migraine, familial hemiplegic, 2 MONDO:0011232, alternating hemiplegia of childhood OMIM:104290, alternating hemiplegia of childhood 1 MONDO:0007087
R-numbers: R57
Signed-off version 1.137
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
familial basilar migraine 602481, familial hemiplegic migraine type 2, 602481, alternating hemiplegia of childhood 104290, Dystonia, migraine
R-numbers: R59
Signed-off version 2.2
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Alternating hemiplegia of childhood 1, 104290, Migraine, familial basilar, 602481, Migraine, familial hemiplegic, 2, 602481, benign familial infantile convulsions, epilepsy and migraine, occipitotemporal epilepsy, infantile epileptic syndrome
R-numbers: R54
Signed-off version 2.13
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Alternating hemiplegia of childhood 1, 104290, Familial hemiplegic migraine 2, 602481
R-numbers: R66
Signed-off version 1.2
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Migraine, familial hemiplegic, 2, 602481, Migraine, familial basilar, 602481, alternating hemiplegia of childhood 104290
R-numbers: R76
Signed-off version 1.2
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Migraine, familial hemiplegic, 2, 602481, Alternating hemiplegia of childhood 1, 104290, Hypokalaemic periodic paralysis