About   Help   FAQ
Symbol
Name
ID
Lbr
lamin B receptor
MGI:2138281
Phenotype annotations related to nervous system
Darker colors indicate more annotations
Human Phenotypes
Lower limb hypertonia
Intellectual disability
Lower limb hyperreflexia
Global developmental delay
Seizures
Generalized tonic-clonic seizures
Disease(s) Associated with LBR
Pelger-Huet anomaly

Mouse Phenotypes
increased neuron apoptosis
abnormal nervous system morphology
hydrocephaly
enlarged lateral ventricles
dilated lateral ventricles
gliosis
Availability Mouse Genotype
LbrGt(XE569)Byg/LbrGt(XE569)Byg
Lbric-2J/Lbric-2J
Lbric-3J/Lbric-3J
Lbric-J/Lbric-J

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)
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
02/18/2020
MGI 6.14
The Jackson Laboratory