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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Impa1
inositol (myo)-1(or 4)-monophosphatase 1
MGI:1933158
20 phenotypes from 3 alleles in 3 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Impa1Rgsc01827/Impa1Rgsc01827
B6NJcl.B6JJcl-Impa1Rgsc01827/Rbrc
no abnormal phenotype detected J:250420
Impa1Rgsc01846/Impa1Rgsc01846
B6NJcl.B6JJcl-Impa1Rgsc01846/Rbrc
abnormal Meckel's cartilage morphology J:250420
abnormal tongue morphology J:250420
asymmetric sternocostal joints J:250420
normal behavior/neurological phenotype J:250420
cleft palate J:250420
normal craniofacial phenotype J:250420
decreased fetal size J:250420
exencephaly J:250420
hyperactivity J:250420
perinatal lethality, incomplete penetrance J:250420
premature death J:250420
prolonged circadian behavior period J:250420
seizures J:250420
small mandible J:250420
Impa1tm1Lex/Impa1tm1Lex
involves: 129S5/SvEvBrd * C57BL/6
embryonic lethality during organogenesis, incomplete penetrance J:157887
hyperactivity J:157887
increased susceptibility to pharmacologically induced seizures J:157887
increased vertical activity J:157887
increased vertical stereotypic behavior J:157887
normal nervous system phenotype J:157887

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