| Primary Identifier | MGI:1857092 | Allele Type | Spontaneous |
| Gene | Atp2b2 | Inheritance Mode | Recessive |
| Strain of Origin | BALB/cAnN | Is Recombinase | false |
| Is Wild Type | false |
| molecularNote | A G-to-A transition point mutation at position 1234 is predicted to cause a glutamine to lysine substitution at position 412 in the encoded protein possibly leading to altered calcium transport from the cytosol to the extracellular space. |
