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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Pemt
phosphatidylethanolamine N-methyltransferase
MGI:104535
14 phenotypes from multigenic genotypes
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Allelic Composition
Genetic Background
Annotated Term Reference
Abcb4tm1Bor/Abcb4tm1Bor
Pemttm1J/Pemttm1J
involves: 129P2/OlaHsd * C57BL/6 * FVB/N
abnormal intestine physiology J:175015
decreased bile salt level J:175015
decreased circulating alanine transaminase level J:175015
increased feces bile salt level J:175015
normal liver/biliary system phenotype J:175015
Pemttm1J/Pemttm1J
tnyw/tnyw
B6;129P2 Pemttm1J-tnyw/GrsrJ
abnormal locomotor coordination J:125079
brain vacuoles J:125079
decreased body size J:125079
normal endocrine/exocrine gland phenotype J:125079
normal hearing/vestibular/ear phenotype J:125079
impaired limb coordination J:125079
impaired righting response J:125079
postnatal lethality, incomplete penetrance J:125079
premature death J:125079

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
12/10/2024
MGI 6.24
The Jackson Laboratory