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Symbol
Name
ID 		Lbr
lamin B receptor
MGI:2138281
Phenotype annotations related to integument
Darker colors indicate more annotations
Human Phenotypes
Xanthelasma
Dermatographic urticaria
Jaundice
Eczematoid dermatitis
Hyperpigmentation of the skin
Pruritus
Disease(s) Associated with LBR
Pelger-Huet anomaly
primary biliary cholangitis

Mouse Phenotypes
decreased subcutaneous adipose tissue amount
abnormal coat/ hair morphology
abnormal hair growth
delayed hair appearance
sparse hair
dilated piliary canal
abnormal vibrissa morphology
absent vibrissae
short vibrissae
abnormal skin morphology
abnormal epidermal layer morphology
abnormal epidermis stratum corneum morphology
hyperkeratosis
orthokeratosis
abnormal epidermis stratum granulosum morphology
increased keratohyalin granule size
epidermis stratum spinosum hyperplasia
epidermal hyperplasia
dry skin
scaly skin
abnormal skin condition
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
Lbric/Lbric
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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Send questions and comments to User Support. 		last database update
04/30/2024
MGI 6.23 		The Jackson Laboratory