About   Help   FAQ
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
abnormal eye physiology
Availability Mouse Genotype
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)
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
02/11/2020
MGI 6.14
The Jackson Laboratory