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Symbol
Name
ID
Atp1a2
ATPase, Na+/K+ transporting, alpha 2 polypeptide
MGI:88106
Phenotype annotations related to muscle
Darker colors indicate more annotations
Human Phenotypes
Facial hypotonia
Rigidity
Hypotonia
Disease(s) Associated with ATP1A2
alternating hemiplegia of childhood
developmental and epileptic encephalopathy 98

Mouse Phenotypes
abnormal cardiac muscle contractility
decreased cardiac muscle contractility
abnormal muscle contractility
Availability Mouse Genotype
Atp1a2tm3Ling/Atp1a2tm3Ling
Atp1a2tm2Ling/Atp1a2+

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
04/09/2024
MGI 6.23
The Jackson Laboratory