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Symbol
Name
ID
Lbr
lamin B receptor
MGI:2138281
Phenotype annotations related to nervous system
Darker colors indicate more annotations
Human Phenotypes
Orthostatic hypotension
Intellectual disability
Excessive daytime somnolence
Sleep abnormality
Lower limb hyperreflexia
Hepatic encephalopathy
Global developmental delay
Seizure
Bilateral tonic-clonic seizure
Disease(s) Associated with LBR
Pelger-Huet anomaly
primary biliary cholangitis

Mouse Phenotypes
increased neuron apoptosis
abnormal nervous system morphology
hydrocephaly
enlarged lateral ventricles
dilated lateral ventricle
gliosis
decreased prepulse inhibition
Availability Mouse Genotype
Lbrem1(IMPC)Tcp/Lbrem1(IMPC)Tcp
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)
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last database update
04/23/2024
MGI 6.23
The Jackson Laboratory