Symbol Name ID |
Lbr
lamin B receptor MGI:2138281 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Neonatal death |
Stillbirth |
Disease(s) Associated with LBR | ||
Greenberg dysplasia |
Mouse Phenotypes | mortality/aging |
premature death |
perinatal lethality |
perinatal lethality, incomplete penetrance |
postnatal lethality |
postnatal lethality, incomplete penetrance |
prenatal lethality |
prenatal lethality, incomplete penetrance |
preweaning lethality, incomplete penetrance |
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Availability | Mouse Genotype | |||||||||
Lbrem1(IMPC)Tcp/Lbrem1(IMPC)Tcp | ||||||||||
LbrGt(XE569)Byg/LbrGt(XE569)Byg | ||||||||||
Lbric-2J/Lbric-2J | ||||||||||
Lbric-3J/Lbric-3J | ||||||||||
Lbric-J/Lbric-J | ||||||||||
Lbric/Lbric | ||||||||||
Lbric-J/Lbrlym3 | * |
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 |
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