Symbol Name ID |
Atp13a2
ATPase type 13A2 MGI:1922022 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Bowel incontinence |
Urinary incontinence |
Apathy |
Lethargy |
Aggressive behavior |
Fatigue |
Disease(s) Associated with ATP13A2 | ||||||
hereditary spastic paraplegia 78 | ||||||
Kufor-Rakeb syndrome |
Mouse Phenotypes | behavior/neurological phenotype |
abnormal spatial learning |
abnormal response to novel object |
limb grasping |
abnormal motor coordination/balance |
abnormal gait |
short stride length |
decreased locomotor activity |
abnormal nest building behavior |
|
Availability | Mouse Genotype | |||||||||
Atp13a2tm1.2Wtd/Atp13a2tm1.2Wtd | ||||||||||
Atp13a2tm1Pjsch/Atp13a2tm1Pjsch | * |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
||
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support. |
last database update 08/02/2024 MGI 6.24 |
|
|