|
Symbol Name ID |
Lbr
lamin B receptor MGI:2138281 |
| Darker colors indicate more annotations |
| Human Phenotypes | Frontal bossing |
Calvarial skull defect |
Micrognathia |
Retrognathia |
Hypoplasia of the maxilla |
Sclerosis of skull base |
Decreased skull ossification |
Macrocephaly |
Midface retrusion |
High forehead |
Prominent forehead |
Gingival overgrowth |
Median cleft palate |
Abnormality of the dentition |
Depressed nasal ridge |
Depressed nasal bridge |
Xanthelasma |
Prominent supraorbital ridges |
| Disease(s) Associated with LBR | ||||||||||||||||||
| Greenberg dysplasia | ||||||||||||||||||
| Pelger-Huet anomaly | ||||||||||||||||||
| primary biliary cholangitis |
| Mouse Phenotypes | abnormal cranium morphology |
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| Availability | Mouse Genotype | |
| Lbrem1(IMPC)Tcp/Lbrem1(IMPC)Tcp | ||
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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