71 phenotypes from 4 alleles in 5 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Tnfrsf11bem1(IMPC)Mbp/Tnfrsf11bem1(IMPC)Mbp C57BL/6N-Tnfrsf11bem1(IMPC)Mbp/MbpMmucd	abnormal auditory brainstem response	J:211773
	abnormal bone structure	J:211773
	abnormal brain morphology	J:211773
	abnormal eye morphology	J:211773
	abnormal gait	J:211773
	abnormal kidney morphology	J:211773
	abnormal skin morphology	J:211773
	anophthalmia	J:211773
	blind uterus	J:211773
	corneal opacity	J:211773
	decreased body length	J:211773
	decreased bone mineral content	J:211773
	decreased bone mineral density	J:211773
	decreased brain size	J:211773
	decreased grip strength	J:211773
	decreased locomotor activity	J:211773
	decreased prepulse inhibition	J:211773
	enlarged kidney	J:211773
	increased circulating alkaline phosphatase level	J:211773
	increased circulating phosphate level	J:211773
	preweaning lethality, incomplete penetrance	J:211773
	small spleen	J:211773
Tnfrsf11btm1Eac/Tnfrsf11btm1Eac involves: 129S4/SvJaeSor	abnormal bone structure	J:67105
	abnormal compact bone morphology	J:67105
	abnormal dendritic cell antigen presentation	J:67105
	abnormal immune system morphology	J:67105
	abnormal immune system physiology	J:67105
	abnormal immunoglobulin level	J:67105
	abnormal long bone morphology	J:67105
	abnormal mandible morphology	J:67105
	abnormal pro-B cell differentiation	J:67105
	decreased bone mineral density	J:67105
	increased B cell number	J:67105
	increased diameter of long bones	J:67105
	increased immature B cell number	J:67105
	increased pro-B cell number	J:67105
	short femur neck	J:67105
Tnfrsf11btm1Khs/Tnfrsf11btm1Khs B6.129P2-Tnfrsf11btm1Khs	abnormal bone remodeling	J:117756
	abnormal inner ear morphology	J:117756
	abnormal malleus morphology	J:117756
	abnormal middle ear morphology	J:117756
	abnormal otic capsule morphology	J:117756
	abnormal stapes footplate morphology	J:117756
	absent distortion product otoacoustic emissions	J:117756
	deafness	J:117756
	increased or absent distortion product otoacoustic emission threshold	J:117756
	increased or absent threshold for auditory brainstem response	J:117756
	increased susceptibility to age-related hearing loss	J:117756
	osteoporosis	J:117756
	otosclerosis	J:117756
Tnfrsf11btm1Khs/Tnfrsf11btm1Khs involves: 129P2/OlaHsd * C57BL/6	abnormal bone structure	J:111153
	abnormal incus body morphology	J:111153
	abnormal inner ear morphology	J:111153
	abnormal long bone epiphyseal plate morphology	J:48325
	abnormal malleus morphology	J:111153
	abnormal middle ear morphology	J:111153
	abnormal middle ear ossicle morphology	J:111153
	abnormal osteoclast differentiation	J:48325, J:111153
	abnormal osteoclast physiology	J:111153
	abnormal skeleton development	J:111153
	abnormal skeleton physiology	J:111153
	abnormal stapes annular ligament morphology	J:111153
	abnormal stapes footplate morphology	J:111153
	abnormal stapes morphology	J:111153
	abnormal trabecular bone morphology	J:48325
	decreased bone mineral density	J:48325, J:111153
	fragile skeleton	J:48325
	increased or absent threshold for auditory brainstem response	J:111153
	increased osteoclast cell number	J:80503
	osteoporosis	J:48325
	postnatal growth retardation	J:48325
	postnatal lethality, incomplete penetrance	J:48325
Tnfrsf11btm1Wss/Tnfrsf11b+ either: (involves: 129X1/SvJ * C57BL/6) or (involves: 129X1/SvJ * Black Swiss)	decreased bone mineral density	J:47602
Tnfrsf11btm1Wss/Tnfrsf11btm1Wss either: (involves: 129X1/SvJ * C57BL/6) or (involves: 129X1/SvJ * Black Swiss)	abnormal compact bone morphology	J:47602
	abnormal long bone epiphysis morphology	J:47602
	abnormal osteoblast morphology	J:47602
	abnormal osteoclast morphology	J:47602
	abnormal parietal bone morphology	J:47602
	absent bone trabeculae	J:47602
	calcified artery	J:47602
	decreased body size	J:47602
	decreased bone mineral density	J:47602
	decreased trabecular bone mass	J:47602
	fragile skeleton	J:47602
	osteoporosis	J:47602
	postnatal lethality, incomplete penetrance	J:47602
	thin parietal bone	J:47602