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 | Increased circulating IgA level |
Increased circulating IgM level |
Abnormality of chromosome segregation |
Increased nuchal translucency |
Conjugated hyperbilirubinemia |
Abnormal circulating lipid concentration |
Hypercholesterolemia |
Hypoalbuminemia |
Elevated gamma-glutamyltransferase level |
Elevated circulating alkaline phosphatase concentration |
Hydrops fetalis |
Nonimmune hydrops fetalis |
Lymphedema |
Ascites |
Hepatic calcification |
Epiphyseal stippling |
Anterior rib punctate calcifications |
Costal cartilage calcification |
Sternal punctate calcifications |
Ectopic calcification |
Laryngeal calcification |
Tracheal calcification |
Disease(s) Associated with LBR | ||||||||||||||||||||||
Greenberg dysplasia | ||||||||||||||||||||||
Pelger-Huet anomaly | ||||||||||||||||||||||
primary biliary cholangitis |
Mouse Phenotypes | homeostasis/metabolism phenotype |
decreased circulating alkaline phosphatase level |
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Availability | Mouse Genotype | ||
Lbrem1(IMPC)Tcp/Lbrem1(IMPC)Tcp | |||
LbrGt(XE569)Byg/LbrGt(XE569)Byg | * |
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 04/23/2024 MGI 6.23 |
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