51 phenotypes from 4 alleles in 10 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Cx3cr1em1(IMPC)Mbp/Cx3cr1em1(IMPC)Mbp C57BL/6N-Cx3cr1em1(IMPC)Mbp/MbpMmucd	abnormal caudal vertebrae morphology	J:211773
	abnormal kidney morphology	J:211773
	enlarged kidney	J:211773
	small kidney	J:211773
Cx3cr1tm1Ifc/Cx3cr1tm1Ifc involves: 129S4/SvJae * C57BL/6	abnormal NK cell physiology	J:82033
	abnormal response to transplant	J:82033
	normal immune system phenotype	J:82033
	impaired macrophage chemotaxis	J:82033
Cx3cr1tm1Litt/Cx3cr1+ B6.129P2-Cx3cr1tm1Litt	increased susceptibility to experimental autoimmune encephalomyelitis	J:129712
	microgliosis	J:110266
	paresis	J:129712
Cx3cr1tm1Litt/Cx3cr1tm1Litt B6.129P2(Cg)-Cx3cr1tm1Litt/J	normal homeostasis/metabolism phenotype	J:139390
Cx3cr1tm1Litt/Cx3cr1tm1Litt B6.129P2-Cx3cr1tm1Litt	abnormal leukocyte physiology	J:124722
	abnormal microglial cell morphology	J:265696
	abnormal microglial cell physiology	J:110266, J:265696
	abnormal NK cell physiology	J:129712
	abnormal ocular fundus morphology	J:265696
	abnormal photoreceptor connecting cilium morphology	J:265696
	abnormal retina outer nuclear layer morphology	J:265696
	abnormal retina photoreceptor morphology	J:265696
	abnormal vascular wound healing	J:124722
	brain inflammation	J:129712
	brainstem hemorrhage	J:129712
	decreased a-wave amplitude	J:265696
	decreased b-wave amplitude	J:265696
	decreased NK cell number	J:129712
	decreased retina cone cell number	J:265696
	decreased vascular smooth muscle cell proliferation	J:124722
	demyelination	J:129712
	normal immune system phenotype	J:129712
	increased neuron apoptosis	J:110266
	increased susceptibility to dopaminergic neuron neurotoxicity	J:110266
	increased susceptibility to experimental autoimmune encephalomyelitis	J:129712
	increased susceptibility to induced morbidity/mortality	J:129712
	microgliosis	J:110266
	paralysis	J:129712
	retina cone cell degeneration	J:265696
	retina degeneration	J:265696
	retina gliosis	J:265696
	retina outer nuclear layer degeneration	J:265696
	short photoreceptor outer segment	J:265696
Cx3cr1tm1Litt/Cx3cr1tm1Litt C.129P2-Cx3cr1tm1Litt	normal immune system phenotype	J:84544
Cx3cr1tm1Litt/Cx3cr1tm1Litt involves: 129P2/OlaHsd	abnormal dendritic cell physiology	J:95694, J:271242
	abnormal small intestinal villus morphology	J:95694
	decreased inflammatory response	J:271242
	increased dendritic cell number	J:210086
	increased susceptibility to bacterial infection induced morbidity/mortality	J:95694
Cx3cr1tm1Litt/Cx3cr1tm1Litt involves: 129P2/OlaHsd * C57BL/6	abnormal leukocyte physiology	J:162714
	abnormal retina morphology	J:127548
	choroidal neovascularization	J:127548
	decreased monocyte cell number	J:145036
	decreased susceptibility to kidney reperfusion injury	J:162714
	normal immune system phenotype	J:84544
	impaired macrophage chemotaxis	J:162714
	normal nervous system phenotype	J:84544
Cx3cr1tm1Zm/Cx3cr1tm1Zm C.129-Cx3cr1tm1Zm	abnormal retina morphology	J:127548
	abnormal retina photoreceptor layer morphology	J:127548
	retina degeneration	J:127548
Cx3cr1tm1Zm/Cx3cr1tm1Zm involves: 129 * C57BL/6	abnormal retina morphology	J:127548
	abnormal retina photoreceptor layer morphology	J:127548
	choroidal neovascularization	J:127548
	retina degeneration	J:127548
	retina deposits	J:127548
	thin retina outer nuclear layer	J:127548
Cx3cr1tm1Zm/Cx3cr1tm1Zm involves: 129S1/Sv * 129X1/SvJ * C57BL/6	abnormal splenocyte physiology	J:103047