Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
477
Gene name Gene Name - the full gene name approved by the HGNC.
ATPase Na+/K+ transporting subunit alpha 2
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
ATP1A2
Synonyms (NCBI Gene) Gene synonyms aliases
DEE98, FARIMPD, FHM2, MHP2
Disease Acronyms (UniProt) Disease acronyms from UniProt database
DEE98, FARIMPD, FHM2
Chromosome Chromosome number
1
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
1q23.2
Summary Summary of gene provided in NCBI Entrez Gene.
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 o
SNPs SNP information provided by dbSNP.
SNP ID Visualize variation Clinical significance Consequence
rs28933398 T>C Pathogenic Coding sequence variant, missense variant
rs28933399 T>C Pathogenic Coding sequence variant, missense variant
rs28933400 T>C Pathogenic Coding sequence variant, missense variant
rs28933401 G>A Pathogenic, likely-pathogenic Coding sequence variant, missense variant
rs28934002 C>A,T Pathogenic, uncertain-significance Coding sequence variant, missense variant
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT003095 hsa-miR-122-5p Luciferase reporter assay, qRT-PCR 19296470
MIRT048595 hsa-miR-100-5p CLASH 23622248
MIRT047687 hsa-miR-10a-5p CLASH 23622248
MIRT663269 hsa-miR-4524b-3p HITS-CLIP 23824327
MIRT663258 hsa-miR-411-5p HITS-CLIP 23824327
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0001504 Process Neurotransmitter uptake ISS
GO:0001662 Process Behavioral fear response ISS
GO:0002026 Process Regulation of the force of heart contraction ISS
GO:0002087 Process Regulation of respiratory gaseous exchange by nervous system process ISS
GO:0005391 Function P-type sodium:potassium-exchanging ATPase activity IBA 21873635
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
182340 800 ENSG00000018625
Protein
UniProt ID P50993
Protein name Sodium/potassium-transporting ATPase subunit alpha-2 (Na(+)/K(+) ATPase alpha-2 subunit) (EC 7.2.2.13) (Sodium pump subunit alpha-2)
Protein function This is the catalytic component of the active enzyme, which catalyzes the hydrolysis of ATP coupled with the exchange of sodium and potassium ions across the plasma membrane. This action creates the electrochemical gradient of sodium and potassi
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00690 Cation_ATPase_N 41 109 Cation transporter/ATPase, N-terminus Domain
PF00122 E1-E2_ATPase 161 352 Family
PF13246 Cation_ATPase 424 518 Family
PF00689 Cation_ATPase_C 796 1005 Cation transporting ATPase, C-terminus Family
Sequence
MGRGAGREYSPAATTAENGGGKKKQKEKELDELKKEVAMDDHKLSLDELGRKYQVDLSKG
LTNQRAQDVLARDGPNALTPPPTTPEWVKFCRQLFGGFSILLWIGAILC
FLAYGIQAAME
DEPSNDNLYLGVVLAAVVIVTGCFSYYQEAKSSKIMDSFKNMVPQQALVIREGEKMQINA
EEVVVGDLVEVKGGDRVPADLRIISSHGCKVDNSSLTGESEPQTRSPEFTHENPLETRNI
CFFSTNCVEGTARGIVIATGDRTVMGRIATLASGLEVGRTPIAMEIEHFIQLITGVAVFL
GVSFFVLSLILGYSWLEAVIFLIGIIVANVPEGLLATVTVCLTLTAKRMARK
NCLVKNLE
AVETLGSTSTICSDKTGTLTQNRMTVAHMWFDNQIHEADTTEDQSGATFDKRSPTWTALS
RIAGLCNRAVFKAGQENISVSKRDTAGDASESALLKCIELSCGSVRKMRDRNPKVAEIPF
NSTNKYQLSIHEREDSPQSHVLVMKGAPERILDRCSTI
LVQGKEIPLDKEMQDAFQNAYM
ELGGLGERVLGFCQLNLPSGKFPRGFKFDTDELNFPTEKLCFVGLMSMIDPPRAAVPDAV
GKCRSAGIKVIMVTGDHPITAKAIAKGVGIISEGNETVEDIAARLNIPMSQVNPREAKAC
VVHGSDLKDMTSEQLDEILKNHTEIVFARTSPQQKLIIVEGCQRQGAIVAVTGDGVNDSP
ALKKADIGIAMGISGSDVSKQAADMILLDDNFASIVTGVEEGRLIFDNLKKSIAYTLTSN
IPEITPFLLFIIANIPLPLGTVTILCIDLGTDMVPAISLAYEAAESDIMKRQPRNSQTDK
LVNERLISMAYGQIGMIQALGGFFTYFVILAENGFLPSRLLGIRLDWDDRTMNDLEDSYG
QEWTYEQRKVVEFTCHTAFFASIVVVQWADLIICKTRRNSVFQQGMKNKILIFGLLEETA
LAAFLSYCPGMGVALRMYPLKVTWWFCAFPYSLLIFIYDEVRKLI
LRRYPGGWVEKETYY
Sequence length 1020
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  cGMP-PKG signaling pathway
cAMP signaling pathway
Cardiac muscle contraction
Adrenergic signaling in cardiomyocytes
Cytoskeleton in muscle cells
Insulin secretion
Thyroid hormone synthesis
Thyroid hormone signaling pathway
Aldosterone synthesis and secretion
Aldosterone-regulated sodium reabsorption
Endocrine and other factor-regulated calcium reabsorption
Proximal tubule bicarbonate reclamation
Salivary secretion
Gastric acid secretion
Pancreatic secretion
Carbohydrate digestion and absorption
Protein digestion and absorption
Bile secretion
Mineral absorption
  Ion homeostasis
Ion transport by P-type ATPases
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Alternating hemiplegia Alternating hemiplegia of childhood, ALTERNATING HEMIPLEGIA OF CHILDHOOD 1 rs267606670, rs28934002, rs387907281, rs387907282, rs398122887, rs587777771, rs606231441, rs606231437, rs606231435, rs80356532, rs542652468, rs765909830, rs80356537, rs1555865401, rs886041431
View all (5 more)
15286158, 12953268, 18056581, 12539047, 15174025
Apraxia Apraxias rs121908377, rs121908378, rs1135401820, rs1178491246, rs1584969672
Arthrogryposis multiplex congenita Arthrogryposis rs1586285494, rs80358233, rs137853305, rs1559154278, rs398124167, rs398124172, rs587780399, rs786204576, rs786204430, rs769345284, rs749355583, rs793888524, rs793888525, rs878854368, rs555445835
View all (138 more)
30690204
Epilepsy Epilepsy rs113994140, rs28937874, rs1589762127, rs104894166, rs28939075, rs2134001459, rs104894167, rs119488099, rs119488100, rs387906420, rs121917752, rs121918622, rs281865564, rs387907313, rs397514670
View all (165 more)
30690204
Unknown
Disease term Disease name Evidence References Source
Migraine with aura Migraine with Aura ClinVar
Associations from Text Mining
Disease Name Relationship Type References
Abnormalities Drug Induced Associate 31586957
Acute Febrile Encephalopathy Associate 23761507
Adrenal Hyperplasia Congenital Associate 35177115
Alternating hemiplegia of childhood Associate 33794876, 35177115, 36749827
Aphasia Associate 23761507
Ataxia Associate 31586957
Autistic Disorder Associate 19454485
Blast Crisis Associate 33557955
Bovine Respiratory Disease Complex Associate 22661290
Brain Diseases Associate 33493807, 36749827, 39667411