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
RS121918614 Health Risk Conflicting classifications of pathogenicity Migraine, familial hemiplegic, 2
RS121918620 Health Risk Conflicting classifications of pathogenicity Migraine, familial hemiplegic, 2
RS1226796744 Health Risk Conflicting classifications of pathogenicity Familial hemiplegic migraine, Familial hemiplegic migraine
RS1236883845 Health Risk Conflicting classifications of pathogenicity Familial hemiplegic migraine, Inborn genetic diseases, Familial hemiplegic migraine
RS139229302 Health Risk Conflicting classifications of pathogenicity Familial hemiplegic migraine, Alternating hemiplegia of childhood 1, Migraine
RS139243866 Health Risk Conflicting classifications of pathogenicity Familial hemiplegic migraine, Familial hemiplegic migraine
RS139499540 Health Risk Conflicting classifications of pathogenicity Familial hemiplegic migraine, Alternating hemiplegia of childhood 1, Fetal akinesia
RS141467566 Health Risk Conflicting classifications of pathogenicity Familial hemiplegic migraine, Alternating hemiplegia of childhood 1, Migraine
RS1422290691 Health Risk Conflicting classifications of pathogenicity Familial hemiplegic migraine, Familial hemiplegic migraine
RS142309356 Health Risk Conflicting classifications of pathogenicity Familial hemiplegic migraine, Familial hemiplegic migraine
RS142348542 Health Risk Conflicting classifications of pathogenicity Alternating hemiplegia of childhood 1, Familial hemiplegic migraine, Migraine
RS143969080 Health Risk Conflicting classifications of pathogenicity Alternating hemiplegia of childhood 1, Migraine, familial hemiplegic
RS144106169 Health Risk Conflicting classifications of pathogenicity Familial hemiplegic migraine, Inborn genetic diseases, ATP1A2-related disorder
RS145701604 Health Risk Conflicting classifications of pathogenicity Migraine, familial hemiplegic, 2
RS146839867 Health Risk Conflicting classifications of pathogenicity Familial hemiplegic migraine, Alternating hemiplegia of childhood 1, Migraine
RS149286529 Health Risk Conflicting classifications of pathogenicity Familial hemiplegic migraine, Inborn genetic diseases, Familial hemiplegic migraine
RS1553244740 Health Risk Conflicting classifications of pathogenicity Familial hemiplegic migraine, Familial hemiplegic migraine
RS1553244875 Health Risk Conflicting classifications of pathogenicity Familial hemiplegic migraine, Familial hemiplegic migraine
RS1553245780 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS1570987954 Health Risk Conflicting classifications of pathogenicity Familial hemiplegic migraine, Developmental and epileptic encephalopathy 98, Familial hemiplegic migraine
RS1570995017 Health Risk Conflicting classifications of pathogenicity Migraine, familial hemiplegic, 2
RS1651741944 Health Risk Conflicting classifications of pathogenicity Familial hemiplegic migraine, Familial hemiplegic migraine
RS1651959213 Health Risk Conflicting classifications of pathogenicity Migraine, familial hemiplegic, 2
RS1651972956 Health Risk Conflicting classifications of pathogenicity Migraine, familial hemiplegic, 2
RS183455719 Health Risk Conflicting classifications of pathogenicity Migraine, familial hemiplegic, 2
RS187733403 Health Risk Conflicting classifications of pathogenicity Alternating hemiplegia of childhood 1, Familial hemiplegic migraine, Migraine
RS202094576 Health Risk Conflicting classifications of pathogenicity Familial hemiplegic migraine, Familial hemiplegic migraine
RS2101988461 Health Risk Conflicting classifications of pathogenicity Familial hemiplegic migraine, See cases, Familial hemiplegic migraine
RS2524859328 Health Risk Conflicting classifications of pathogenicity Migraine, familial hemiplegic, 2
RS2524889994 Health Risk Conflicting classifications of pathogenicity See cases, See cases
RS28934002 Health Risk Conflicting classifications of pathogenicity Alternating hemiplegia of childhood 1, Familial hemiplegic migraine, ATP1A2-related disorder
RS369061211 Health Risk Conflicting classifications of pathogenicity Migraine, familial hemiplegic, 2
RS369898494 Health Risk Conflicting classifications of pathogenicity Familial hemiplegic migraine, Familial hemiplegic migraine
RS370023134 Health Risk Conflicting classifications of pathogenicity Familial hemiplegic migraine, Familial hemiplegic migraine
RS370111257 Health Risk Conflicting classifications of pathogenicity Familial hemiplegic migraine, Familial hemiplegic migraine
RS371086182 Health Risk Conflicting classifications of pathogenicity Familial hemiplegic migraine, Familial hemiplegic migraine
RS371257019 Health Risk Conflicting classifications of pathogenicity Familial hemiplegic migraine, Inborn genetic diseases, Familial hemiplegic migraine
RS373178892 Health Risk Conflicting classifications of pathogenicity Familial hemiplegic migraine, Inborn genetic diseases, ATP1A2-related disorder
RS374355050 Health Risk Conflicting classifications of pathogenicity Familial hemiplegic migraine, Familial hemiplegic migraine
RS374501280 Health Risk Conflicting classifications of pathogenicity Familial hemiplegic migraine, Alternating hemiplegia of childhood 1, Migraine
RS374724827 Health Risk Conflicting classifications of pathogenicity Familial hemiplegic migraine, Inborn genetic diseases, Familial hemiplegic migraine
RS376128790 Health Risk Conflicting classifications of pathogenicity Familial hemiplegic migraine, Alternating hemiplegia of childhood 1, Migraine
RS528454399 Health Risk Conflicting classifications of pathogenicity Alternating hemiplegia of childhood 1, Migraine, familial hemiplegic
RS540087535 Health Risk Conflicting classifications of pathogenicity Familial hemiplegic migraine, Familial hemiplegic migraine
RS55741021 Health Risk Conflicting classifications of pathogenicity Familial hemiplegic migraine, Alternating hemiplegia of childhood 1, Migraine
RS55858252 Health Risk Conflicting classifications of pathogenicity Familial hemiplegic migraine, Alternating hemiplegia of childhood 1, Migraine
RS574788908 Health Risk Conflicting classifications of pathogenicity Familial hemiplegic migraine, Familial hemiplegic migraine
RS575299887 Health Risk Conflicting classifications of pathogenicity Familial hemiplegic migraine, Inborn genetic diseases, Familial hemiplegic migraine
RS587780283 Health Risk Conflicting classifications of pathogenicity Familial hemiplegic migraine, Familial hemiplegic migraine
RS746744495 Health Risk Conflicting classifications of pathogenicity Fetal akinesia, respiratory insufficiency, microcephaly
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