112 phenotypes from 7 alleles in 9 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Lbrem1(IMPC)Tcp/Lbrem1(IMPC)Tcp C57BL/6N-Lbrem1(IMPC)Tcp/Tcp	abnormal bone structure	J:211773
	abnormal coat/ hair morphology	J:211773
	abnormal cranium morphology	J:211773
	abnormal digit morphology	J:211773
	abnormal forelimb morphology	J:211773
	abnormal skin morphology	J:211773
	abnormal tail morphology	J:211773
	absent vibrissae	J:211773
	decreased body length	J:211773
	decreased bone mineral content	J:211773
	decreased bone mineral density	J:211773
	decreased circulating alkaline phosphatase level	J:211773
	decreased exploration in new environment	J:211773
	decreased grip strength	J:211773
	decreased locomotor activity	J:211773
	decreased lymphocyte cell number	J:211773
	decreased mean corpuscular hemoglobin	J:211773
	decreased prepulse inhibition	J:211773
	enlarged lymph nodes	J:211773
	impaired pupillary reflex	J:211773
	increased monocyte cell number	J:211773
	increased neutrophil cell number	J:211773
	preweaning lethality, incomplete penetrance	J:211773
	short tibia	J:211773
	shortened PR interval	J:211773
	small seminal vesicle	J:211773
	small testis	J:211773
LbrGt(XE569)Byg/LbrGt(XE569)Byg involves: 129P2/OlaHsd * C57BL/6Cr	abnormal cell nucleus morphology	J:138854
	abnormal eye physiology	J:138854
	abnormal granulocyte differentiation	J:138854
	abnormal granulocyte morphology	J:138854
	abnormal lymphocyte morphology	J:138854
	abnormal neutrophil morphology	J:138854
	abnormal nuclear lamina morphology	J:138854
	abnormal rib morphology	J:138854
	decreased subcutaneous adipose tissue amount	J:138854
	enlarged lateral ventricles	J:138854
	enlarged lymph nodes	J:138854
	female infertility	J:138854
	gliosis	J:138854
	normal homeostasis/metabolism phenotype	J:138854
	hyperkeratosis	J:138854
	increased neuron apoptosis	J:138854
	male infertility	J:138854
	postnatal lethality, incomplete penetrance	J:138854
	premature death	J:138854
	prenatal lethality, incomplete penetrance	J:138854
	scoliosis	J:138854
	uterus hypoplasia	J:138854
Lbric-2J/Lbric-2J involves: A/J	abnormal blood cell morphology/development	J:80915
	abnormal coat/ hair morphology	J:80915
	abnormal epidermal layer morphology	J:80915
	abnormal immune system cell morphology	J:80915
	abnormal nervous system morphology	J:80915
	decreased body size	J:80915
	perinatal lethality	J:80915
	prenatal lethality	J:80915
Lbric-3J/Lbric-3J involves: A/J	abnormal blood cell morphology/development	J:80915
	abnormal coat/ hair morphology	J:80915
	abnormal epidermal layer morphology	J:80915
	abnormal immune system cell morphology	J:80915
	abnormal nervous system morphology	J:80915
	decreased body size	J:80915
	perinatal lethality	J:80915
	prenatal lethality	J:80915
Lbric-J/Lbr+ (NZW/LacJ x C57BL/6J-Lbric-J/J)F1	abnormal kidney morphology	J:234168
	abnormal neutrophil morphology	J:234168
	abnormal renal glomerulus morphology	J:234168
	enlarged spleen	J:234168
	glomerulosclerosis	J:234168
	increased anti-chromatin antibody level	J:234168
	increased anti-nuclear antigen antibody level	J:234168
	increased autoantibody level	J:234168
	increased susceptibility to systemic lupus erythematosus	J:234168
	renal interstitial fibrosis	J:234168
Lbric-J/Lbr+ C57BL/6J-Lbric-J	abnormal granulocyte morphology	J:80915
Lbric-J/Lbric-J C57BL/6J-Lbric-J	abnormal cell nucleus morphology	J:80915
	abnormal eosinophil morphology	J:80915
	abnormal lymphocyte morphology	J:80915
	abnormal neutrophil morphology	J:80915
	decreased body size	J:80915
	dilated lateral ventricle	J:80915
	dilated piliary canal	J:80915
	epidermal hyperplasia	J:80915
	hydrocephaly	J:80915
	orthokeratosis	J:80915
	perinatal lethality, incomplete penetrance	J:80915
	prenatal lethality, incomplete penetrance	J:80915
	scaly skin	J:80915
	sparse hair	J:80915
	syndactyly	J:80915
Lbric-J/Lbric-J involves: 129S4/SvJae * C57BL/6	abnormal long bone epiphyseal plate morphology	J:143838
	abnormal neutrophil differentiation	J:143838
	abnormal spleen morphology	J:143838
	abnormal trabecular bone morphology	J:143838
	dry skin	J:143838
	postnatal growth retardation	J:143838
	scaly skin	J:143838
	sparse hair	J:143838
	syndactyly	J:143838
Lbric-J/Lbrlym3 C57BL/6-Lbric-J/Lbrlym3	decreased leukocyte cell number	J:180355
	decreased lymphocyte cell number	J:180355
	normal mortality/aging	J:180355
Lbric/Lbr+ Not Specified	abnormal cell nucleus morphology	J:5569
Lbric/Lbric Not Specified	abnormal cell nucleus morphology	J:5569
	abnormal epidermal layer morphology	J:5552
	abnormal epidermis stratum corneum morphology	J:13065
	abnormal epidermis stratum granulosum morphology	J:5740
	abnormal hair growth	J:13065
	abnormal respiration	J:13065
	abnormal skin condition	J:13065
	abnormal vibrissa morphology	J:13065
	absent scrotum	J:13065
	constricted vagina orifice	J:13065
	cryptorchism	J:13065
	decreased vocalization	J:13065
	delayed hair appearance	J:13065
	epidermis stratum spinosum hyperplasia	J:13065
	increased keratohyalin granule size	J:5740
	increased mitochondrial fission	J:5740
	male infertility	J:13065
	postnatal growth retardation	J:13065
	postnatal lethality	J:13065
	reduced female fertility	J:13065
	scaly skin	J:13065
	short vibrissae	J:13065
	tail necrosis	J:13065
Lbrlym3/Lbr+ C57BL/6-Lbrlym3	abnormal neutrophil morphology	J:180355
Lbrlym3/Lbrlym3 C57BL/6-Lbrlym3	abnormal B cell physiology	J:180355
	abnormal blood cell morphology/development	J:180355
	abnormal lymphocyte cell number	J:180355
	abnormal lymphocyte morphology	J:180355
	abnormal neutrophil morphology	J:180355
	abnormal T cell physiology	J:180355
	decreased B cell number	J:180355
	decreased CD4-positive, alpha-beta T cell number	J:180355
	decreased CD8-positive, alpha-beta T cell number	J:180355
	decreased leukocyte cell number	J:180355
	decreased lymphocyte cell number	J:180355
	decreased T cell number	J:180355
	decreased T cell proliferation	J:180355
	lymph node hypoplasia	J:180355
	normal skeleton phenotype	J:180355
	spleen hypoplasia	J:180355
	thymus hypoplasia	J:180355