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Symbol
Name
ID
Lbr
lamin B receptor
MGI:2138281
Phenotype annotations related to vision/eye
Darker colors indicate more annotations
Human Phenotypes
Hypertelorism
Strabismus
Disease(s) Associated with LBR
Greenberg dysplasia
Pelger-Huet anomaly

Mouse Phenotypes
impaired pupillary reflex
abnormal eye physiology
Availability Mouse Genotype
Lbrem1(IMPC)Tcp/Lbrem1(IMPC)Tcp
LbrGt(XE569)Byg/LbrGt(XE569)Byg

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
04/16/2024
MGI 6.23
The Jackson Laboratory