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Symbol
Name
ID
Lmnb1
lamin B1
MGI:96795
Phenotype annotations related to skeleton
Darker colors indicate more annotations
Human Phenotypes
Microcephaly
Flexion contracture
Abnormal cortical bone morphology
Disease(s) Associated with LMNB1
adult-onset autosomal dominant demyelinating leukodystrophy
primary autosomal recessive microcephaly

Mouse Phenotypes
abnormal coronal suture morphology
abnormal sagittal suture morphology
abnormal cranium morphology
abnormal thoracic vertebrae morphology
abnormal spine curvature
delayed bone ossification
Availability Mouse Genotype
Lmnb1Gt(XA130)Byg/Lmnb1Gt(XA130)Byg
Lmnb1tm2Sgy/Lmnb1tm2Sgy

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
04/23/2024
MGI 6.23
The Jackson Laboratory