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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Atp13a2
ATPase type 13A2
MGI:1922022
19 phenotypes from 2 alleles in 2 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Atp13a2tm1.2Wtd/Atp13a2tm1.2Wtd
involves: 129 * C57BL/6
abnormal lysosome morphology J:221680
abnormal lysosome physiology J:221680
abnormal neuron morphology J:221680
astrocytosis J:221680
decreased locomotor activity J:221680
gliosis J:221680
impaired autophagy J:221680
limb grasping J:221680
lipofuscinosis J:221680
lysosomal protein accumulation J:221680
Atp13a2tm1Pjsch/Atp13a2tm1Pjsch
involves: 129S6/SvEvTac * Black Swiss
abnormal gait J:194306
abnormal motor coordination/balance J:194306
abnormal nest building behavior J:194306
abnormal neuron morphology J:194306
abnormal response to novel object J:194306
abnormal spatial learning J:194306
alpha-synuclein inclusion body J:194306
normal behavior/neurological phenotype J:194306
lipofuscinosis J:194306
normal nervous system phenotype J:194306
short stride length J:194306

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
04/23/2024
MGI 6.23
The Jackson Laboratory