ATP1A2 Chromosome 1

ATPase Na+/K+ transporting subunit alpha 2
187 variants 187 Health Risk

Upload your DNA to see your personal genotypes for variants in ATP1A2.

What This Gene Does
The protein encoded by this gene belongs to the family of P-type cation transport ATPases, and to the subfamily of Na+/K+ -ATPases. Na+/K+ -ATPase is an integral membrane protein responsible for establishing and maintaining the electrochemical gradients of Na and K ions across the plasma membrane. These gradients are essential for osmoregulation, for sodium-coupled transport of a variety of organic and inorganic molecules, and for electrical excitability of nerve and muscle. This enzyme is composed of two subunits, a large catalytic subunit (alpha) and a smaller glycoprotein subunit (beta). The catalytic subunit of Na+/K+ -ATPase is encoded by multiple genes. This gene encodes an alpha 2 subunit. Mutations in this gene result in familial basilar or hemiplegic migraines, and in a rare syndrome known as alternating hemiplegia of childhood. [provided by RefSeq, Oct 2008]
Gene Info
Gene Group
ATPase Na+/K+ transporting subunits
Locus Type
gene with protein product
Location
1q23.2
Ensembl
ENSG00000018625
Associated Conditions (21)
Migraine
familial hemiplegic
2
Familial hemiplegic migraine
Inborn genetic diseases
Alternating hemiplegia of childhood 1
Fetal akinesia
respiratory insufficiency
microcephaly
polymicrogyria
and dysmorphic facies
Developmental and epileptic encephalopathy 98
ATP1A2-related disorder
See cases
Hemiplegic migraine-developmental and epileptic encephalopathy spectrum
Epileptic encephalopathy
Alternating hemiplegia of childhood
familial basilar
Polymicrogyria
Spastic ataxia
+1 more conditions
Key Variants
RS121918614
Conflicting classifications of pathogenicity
Migraine, familial hemiplegic, 2
Health Risk
RS121918620
Conflicting classifications of pathogenicity
Migraine, familial hemiplegic, 2
Health Risk
RS1226796744
Conflicting classifications of pathogenicity
Familial hemiplegic migraine, Familial hemiplegic migraine
Health Risk
RS1236883845
Conflicting classifications of pathogenicity
Familial hemiplegic migraine, Inborn genetic diseases, Familial hemiplegic migraine
Health Risk
RS139229302
Conflicting classifications of pathogenicity
Familial hemiplegic migraine, Alternating hemiplegia of childhood 1, Migraine
Health Risk
RS139243866
Conflicting classifications of pathogenicity
Familial hemiplegic migraine, Familial hemiplegic migraine
Health Risk
RS139499540
Conflicting classifications of pathogenicity
Familial hemiplegic migraine, Alternating hemiplegia of childhood 1, Fetal akinesia
Health Risk
RS141467566
Conflicting classifications of pathogenicity
Familial hemiplegic migraine, Alternating hemiplegia of childhood 1, Migraine
Health Risk
RS1422290691
Conflicting classifications of pathogenicity
Familial hemiplegic migraine, Familial hemiplegic migraine
Health Risk
RS142309356
Conflicting classifications of pathogenicity
Familial hemiplegic migraine, Familial hemiplegic migraine
Health Risk
RS142348542
Conflicting classifications of pathogenicity
Alternating hemiplegia of childhood 1, Familial hemiplegic migraine, Migraine
Health Risk
RS143969080
Conflicting classifications of pathogenicity
Alternating hemiplegia of childhood 1, Migraine, familial hemiplegic
Health Risk
All Variants (187)
RSID Category Clinical Significance Conditions
RS746795369 Health Risk Conflicting classifications of pathogenicity Familial hemiplegic migraine, Familial hemiplegic migraine
RS747238010 Health Risk Conflicting classifications of pathogenicity Familial hemiplegic migraine, Familial hemiplegic migraine
RS747283283 Health Risk Conflicting classifications of pathogenicity Familial hemiplegic migraine, Alternating hemiplegia of childhood 1, Migraine
RS747542544 Health Risk Conflicting classifications of pathogenicity Familial hemiplegic migraine, Familial hemiplegic migraine
RS747886840 Health Risk Conflicting classifications of pathogenicity Familial hemiplegic migraine, Inborn genetic diseases, Familial hemiplegic migraine
RS749326394 Health Risk Conflicting classifications of pathogenicity Familial hemiplegic migraine, Alternating hemiplegia of childhood 1, Developmental and epileptic encephalopathy 98
RS751808345 Health Risk Conflicting classifications of pathogenicity Familial hemiplegic migraine, Familial hemiplegic migraine
RS754699681 Health Risk Conflicting classifications of pathogenicity Familial hemiplegic migraine, Inborn genetic diseases, Migraine
RS754878991 Health Risk Conflicting classifications of pathogenicity Familial hemiplegic migraine, Familial hemiplegic migraine
RS755310507 Health Risk Conflicting classifications of pathogenicity Familial hemiplegic migraine, Migraine, familial hemiplegic
RS759781800 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Familial hemiplegic migraine, Inborn genetic diseases
RS763041955 Health Risk Conflicting classifications of pathogenicity Familial hemiplegic migraine, Migraine, familial hemiplegic
RS763782107 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Familial hemiplegic migraine, Inborn genetic diseases
RS764559670 Health Risk Conflicting classifications of pathogenicity Alternating hemiplegia of childhood 1, Migraine, familial hemiplegic
RS765818392 Health Risk Conflicting classifications of pathogenicity Familial hemiplegic migraine, Familial hemiplegic migraine
RS765936799 Health Risk Conflicting classifications of pathogenicity Familial hemiplegic migraine, Fetal akinesia, respiratory insufficiency
RS767230468 Health Risk Conflicting classifications of pathogenicity Familial hemiplegic migraine, Inborn genetic diseases, Familial hemiplegic migraine
RS768746868 Health Risk Conflicting classifications of pathogenicity Migraine, familial hemiplegic, 2
RS769798147 Health Risk Conflicting classifications of pathogenicity Alternating hemiplegia of childhood 1, Migraine, familial hemiplegic
RS771085157 Health Risk Conflicting classifications of pathogenicity Familial hemiplegic migraine, Alternating hemiplegia of childhood 1, Migraine
RS775031246 Health Risk Conflicting classifications of pathogenicity Alternating hemiplegia of childhood 1, Migraine, familial hemiplegic
RS777716327 Health Risk Conflicting classifications of pathogenicity Familial hemiplegic migraine, Familial hemiplegic migraine
RS779356370 Health Risk Conflicting classifications of pathogenicity Alternating hemiplegia of childhood 1, Migraine, familial hemiplegic
RS779611112 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Familial hemiplegic migraine, Inborn genetic diseases
RS780155641 Health Risk Conflicting classifications of pathogenicity Familial hemiplegic migraine, Familial hemiplegic migraine, Familial hemiplegic migraine
RS781687346 Health Risk Conflicting classifications of pathogenicity Familial hemiplegic migraine, Migraine, familial hemiplegic
RS886039530 Health Risk Conflicting classifications of pathogenicity Epileptic encephalopathy, Familial hemiplegic migraine, Inborn genetic diseases
RS886043454 Health Risk Conflicting classifications of pathogenicity Familial hemiplegic migraine, Familial hemiplegic migraine
RS886045415 Health Risk Conflicting classifications of pathogenicity Migraine, familial hemiplegic, 2
RS915777286 Health Risk Conflicting classifications of pathogenicity Migraine, familial hemiplegic, 2
RS1057521630 Health Risk Likely pathogenic Developmental and epileptic encephalopathy 98, Developmental and epileptic encephalopathy 98, Migraine
RS1064796771 Health Risk Likely pathogenic
RS1085307953 Health Risk Likely pathogenic
RS1219118149 Health Risk Likely pathogenic Familial hemiplegic migraine, Familial hemiplegic migraine
RS121918617 Health Risk Likely pathogenic Migraine, familial hemiplegic, 2
RS1382260409 Health Risk Likely pathogenic Migraine, familial hemiplegic, 2
RS1403515889 Health Risk Likely pathogenic Familial hemiplegic migraine, Fetal akinesia, respiratory insufficiency
RS1421966486 Health Risk Likely pathogenic Familial hemiplegic migraine, Familial hemiplegic migraine
RS1553244022 Health Risk Likely pathogenic
RS1553245183 Health Risk Likely pathogenic
RS1553245908 Health Risk Likely pathogenic
RS1553245943 Health Risk Likely pathogenic Inborn genetic diseases, Familial hemiplegic migraine, Inborn genetic diseases
RS1558009266 Health Risk Likely pathogenic Alternating hemiplegia of childhood 1, Migraine, familial hemiplegic
RS1570988755 Health Risk Likely pathogenic
RS1570994712 Health Risk Likely pathogenic Familial hemiplegic migraine, Familial hemiplegic migraine
RS1651907319 Health Risk Likely pathogenic Migraine, familial hemiplegic, 2
RS1651922528 Health Risk Likely pathogenic
RS1651973884 Health Risk Likely pathogenic
RS1651974671 Health Risk Likely pathogenic Migraine, familial hemiplegic, 2
RS1651975273 Health Risk Likely pathogenic
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