33 phenotypes from 3 alleles in 4 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Lifrtm1b(EUCOMM)Hmgu/Lifr+ C57BL/6N-Lifrtm1b(EUCOMM)Hmgu/H	abnormal brain morphology	J:211773
	decreased exploration in new environment	J:211773
Lifrtm1b(EUCOMM)Hmgu/Lifrtm1b(EUCOMM)Hmgu C57BL/6N-Lifrtm1b(EUCOMM)Hmgu/H	preweaning lethality, complete penetrance	J:211773
Lifrtm1Cgre/Lifrtm1Cgre either: (involves: 129P2/OlaHsd * CBA) or (involves: 129P2/OlaHsd * MF1)	decreased body weight	J:82048
	decreased motor neuron number	J:82048
	neonatal lethality, complete penetrance	J:82048
Lifrtm1Imx/Lifr+ B6;129S7-Lifrtm1Imx/J	abnormal ureter morphology	J:242320
	cryptorchism	J:242320
	hydroureter	J:242320
Lifrtm1Imx/Lifrtm1Imx B6;129S7-Lifrtm1Imx/J	abnormal kidney development	J:242320
	abnormal kidney morphology	J:242320
	abnormal renal/urinary system morphology	J:242320
	abnormal ureter morphology	J:242320
	abnormal ureter smooth muscle morphology	J:242320
	blind ureter	J:242320
	cryptorchism	J:242320
	decreased fetal size	J:242320
	decreased nephron number	J:242320
	decreased renal glomerulus number	J:242320
	ectopic ureter	J:242320
	hydronephrosis	J:242320
	hydroureter	J:242320
	prenatal lethality, incomplete penetrance	J:242320
	renal hypoplasia	J:242320
	small kidney	J:242320
Lifrtm1Imx/Lifrtm1Imx involves: 129P3/J * 129S7/SvEvBrd * C57BL/6	abnormal astrocyte morphology	J:25253
	abnormal dorsal root ganglion morphology	J:25253
	abnormal long bone morphology	J:25253
	abnormal metacarpal bone morphology	J:25253
	abnormal placenta morphology	J:25253
	decreased body size	J:25253
	decreased bone mineral density	J:25253
	decreased bone volume	J:25253
	embryonic lethality before implantation, incomplete penetrance	J:25253
	increased liver glycogen level	J:25253
	increased osteoclast cell number	J:25253
	neonatal lethality, complete penetrance	J:25253