Symbol Name ID |
Pemt
phosphatidylethanolamine N-methyltransferase MGI:104535 |
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 |
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 |
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