Impa1 Phenotype Annotations

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

Allelic Composition Genetic Background	Annotated Term	Reference
Impa1^Rgsc01827/Impa1^Rgsc01827 B6NJcl.B6JJcl-Impa1^Rgsc01827/Rbrc	no abnormal phenotype detected	J:250420
Impa1^Rgsc01846/Impa1^Rgsc01846 B6NJcl.B6JJcl-Impa1^Rgsc01846/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
Impa1^tm1Lex/Impa1^tm1Lex 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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