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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Mnat1
menage a trois 1
MGI:106207
9 phenotypes from 3 alleles in 3 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Egr2tm2(cre)Pch/?
Mnat1tm2Tpm/Mnat1tm2.1Tpm
involves: 129S2/SvPas
abnormal gait J:120170
abnormal Schwann cell precursor morphology J:120170
abnormal spermatogenesis J:120170
decreased lean body mass J:120170
demyelination J:120170
Mnat1tm1Tpm/Mnat1tm1Tpm
either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * CD-1)
abnormal embryonic tissue morphology J:69926
embryonic lethality between implantation and somite formation, complete penetrance J:69926
inner cell mass degeneration J:69926
Mnat1tm2Tpm/Mnat1tm2Tpm
Not Specified
no abnormal phenotype detected J:120170

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
04/16/2024
MGI 6.23
The Jackson Laboratory