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Symbol Name ID |
Lmnb2
lamin B2 MGI:96796 |
| Allelic Composition Genetic Background |
Annotated Term | Reference |
| Lmnb1tm1.1Sgy/Lmnb1tm1.1Sgy Lmnb2tm1.1Sgy/Lmnb2tm1.1Sgy Tg(KRT14-cre)1Cgn/0 involves: 129P2/OlaHsd * C57BL/6 * DBA/2 |
abnormal keratinocyte morphology | J:174963 |
| normal integument phenotype | J:174963 | |
| normal mortality/aging | J:174963 | |
| Lmnb1tm1Yxz/Lmnb1tm1Yxz Lmnb2tm1Yxz/Lmnb2tm1Yxz involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6 |
abnormal cell physiology | J:178993 |
| abnormal neuron differentiation | J:178993 | |
| abnormal neuronal migration | J:178993 | |
| abnormal neuronal precursor proliferation | J:178993 | |
| abnormal phrenic nerve innervation pattern to diaphragm | J:178993 | |
| abnormal pulmonary alveolus morphology | J:178993 | |
| abnormal stratification in cerebral cortex | J:178993 | |
| decreased embryo size | J:178993 | |
| decreased fetal size | J:178993 | |
| increased neuronal precursor cell number | J:178993 | |
| microcephaly | J:178993 | |
| neonatal lethality, complete penetrance | J:178993 | |
| respiratory failure | J:178993 | |
| thin cerebral cortex | J:178993 | |
| thin diaphragm muscle | J:178993 |
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 09/30/2025 MGI 6.24 |
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