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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Pitrm1
pitrilysin metallepetidase 1
MGI:1916867
20 phenotypes from 1 allele in 1 genetic background
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Allelic Composition
Genetic Background
Annotated Term Reference
Pitrm1tm1a(KOMP)Wtsi/Pitrm1+
C57BL/6N-Pitrm1tm1a(KOMP)Wtsi/Wtsi
abnormal cell physiology J:236767
abnormal mitochondrial physiology J:236767
abnormal motor coordination/balance J:236767
amyloid beta deposits J:236767
ataxia J:236767
decreased basal metabolism J:236767
decreased carbon dioxide production J:236767
decreased oxygen consumption J:236767
decreased vertical activity J:236767
gliosis J:236767
impaired coordination J:236767
limb grasping J:236767
neuron degeneration J:236767
positive geotaxis J:236767
Pitrm1tm1a(KOMP)Wtsi/Pitrm1tm1a(KOMP)Wtsi
C57BL/6N-Pitrm1tm1a(KOMP)Wtsi/Wtsi
abnormal chorion morphology J:261316
abnormal placenta morphology J:261316
abnormal trophoblast giant cell morphology J:261316
abnormal trophoblast layer morphology J:261316
embryonic lethality during organogenesis, complete penetrance J:261316
preweaning lethality, complete penetrance J:211773

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
10/09/2024
MGI 6.24
The Jackson Laboratory