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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Lmnb1
lamin B1
MGI:96795
18 phenotypes from multigenic genotypes
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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

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
11/12/2024
MGI 6.24
The Jackson Laboratory