78 phenotypes from 3 alleles in 5 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Csf1rtm1.1Jwp/Csf1rtm1.1Jwp involves: 129/Sv * C57BL/6J * FVB/N * SJL	abnormal skeleton morphology	J:110981
	absent teeth	J:110981
	decreased body size	J:110981
	increased bone mineral density	J:110981
	osteoporosis	J:110981
	premature death	J:110981
	round snout	J:110981
Csf1rtm1Ers/Csf1r+ B6.129X1-Csf1rtm1Ers	abnormal brain white matter morphology	J:219294
	abnormal corpus callosum morphology	J:219294
	abnormal lateral ventricle morphology	J:219294
	abnormal learning/memory/conditioning	J:219294
	ataxia	J:219294
	axonal spheroids	J:219294
	decreased coping response	J:219294
	demyelination	J:219294
	enlarged lateral ventricles	J:219294
	hypermyelination	J:219294
	impaired coordination	J:219294
	impaired olfaction	J:219294
	increased anxiety-related response	J:219294
	increased oligodendrocyte progenitor number	J:219294
	microgliosis	J:219294
	neurodegeneration	J:219294
	neuron degeneration	J:219294
Csf1rtm1Ers/Csf1rtm1Ers FVB.129X1-Csf1rtm1Ers	abnormal bone ossification	J:111489
	abnormal compact bone lamellar structure	J:111489
	abnormal compact bone morphology	J:111489
	abnormal Langerhans cell physiology	J:112594
	abnormal limb morphology	J:111489
	abnormal long bone epiphyseal plate morphology	J:111489
	abnormal long bone epiphyseal plate proliferative zone	J:111489
	abnormal macrophage differentiation	J:112594
	abnormal osteoblast morphology	J:111489
	abnormal osteoclast morphology	J:111489
	abnormal osteocyte dendritic process morphology	J:111489
	abnormal osteocyte morphology	J:111489
	abnormal skeleton morphology	J:111489
	abnormal skeleton physiology	J:111489
	absent Langerhans cell	J:112594
	decreased bone mineralization	J:111489
	decreased bone strength	J:111489
	decreased compact bone thickness	J:111489
	delayed endochondral bone ossification	J:111489
	fragile skeleton	J:111489
	increased width of hypertrophic chondrocyte zone	J:111489
	postnatal lethality, complete penetrance	J:111489
Csf1rtm1Ers/Csf1rtm1Ers involves: 129X1/SvJ * C3Heb/FeJ * C57BL/6J	abnormal blood cell morphology/development	J:73663
	abnormal bone marrow morphology	J:73663
	abnormal bone structure	J:73663
	abnormal circulating cytokine level	J:73663
	abnormal leukocyte cell number	J:73663
	abnormal mammary gland growth during pregnancy	J:73663
	abnormal osteoclast differentiation	J:73663
	abnormal sexual interaction	J:73663
	abnormal skeleton morphology	J:73663
	abnormal spleen morphology	J:73663
	abnormal trabecular bone morphology	J:73663
	deafness	J:73663
	decreased body weight	J:73663
	decreased Langerhans cell number	J:73663
	decreased length of long bones	J:73663
	decreased lymphocyte cell number	J:73663
	decreased macrophage cell number	J:73663
	decreased monocyte cell number	J:73663
	decreased testes secretion	J:73663
	domed cranium	J:73663
	failure of bone resorption	J:73663
	failure of tooth eruption	J:73663
	increased bone mineral density	J:73663
	increased granulocyte number	J:73663
	increased spleen weight	J:73663
	kinked tail	J:73663
	oligozoospermia	J:73663
	osteopetrosis	J:73663
	postnatal growth retardation	J:73663
	postnatal lethality	J:73663
	prolonged diestrus	J:73663
	prolonged estrous cycle	J:73663
	reduced male fertility	J:73663
	short limbs	J:73663
Csf1rtm1Jwp/Csf1rtm1Jwp involves: 129/Sv * C57BL/6J * SJL	no abnormal phenotype detected	J:110981