Symbol Name ID |
Lmnb1
lamin B1 MGI:96795 |
Darker colors indicate more annotations |
Human Phenotypes | Microcephaly |
Sloping forehead |
Thin upper lip vermilion |
Upslanted palpebral fissure |
Disease(s) Associated with LMNB1 | ||||
primary autosomal recessive microcephaly |
Mouse Phenotypes | abnormal coronal suture morphology |
abnormal sagittal suture morphology |
abnormal cranium morphology |
flat head |
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Availability | Mouse Genotype | ||||
Lmnb1Gt(XA130)Byg/Lmnb1Gt(XA130)Byg | |||||
Lmnb1tm2Sgy/Lmnb1tm2Sgy |
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 05/14/2024 MGI 6.23 |
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