65 phenotypes from 6 alleles in 7 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Tcirg1M1Jeau/Tcirg1+ either: (involves: C3H/HeJ * C57BL/6) or (involves: C3H/HeJ * C57BL/6 * FVB/N)	abnormal osteoclast morphology	J:196503
	abnormal osteoclast physiology	J:196503
	abnormal trabecular bone morphology	J:196503
	increased bone mineral content	J:196503
	increased bone mineral density	J:196503
	increased osteoclast cell number	J:196503
	increased trabecular bone mass	J:196503
	normal skeleton phenotype	J:196503
Tcirg1oc/Tcirg1oc B6C3Fe a/a-Tcirg1oc/J	abnormal incisor morphology	J:7870
	abnormal long bone hypertrophic chondrocyte zone	J:7766
	abnormal long bone metaphysis morphology	J:7766, J:7870
	abnormal osteoclast morphology	J:7870
	abnormal predentin morphology	J:7870
	abnormal thyroid gland morphology	J:7870
	circling	J:7870, J:61295
	decreased body size	J:7870, J:61295
	decreased body weight	J:7870
	decreased circulating insulin level	J:116082
	decreased insulin secretion	J:116082
	delayed tooth eruption	J:7870, J:61295
	extramedullary hematopoiesis	J:7870
	failure of bone resorption	J:7766
	increased long bone epiphyseal plate size	J:7766, J:7870
	increased megakaryocyte cell number	J:7870
	increased width of hypertrophic chondrocyte zone	J:7766
	osteopetrosis	J:7870
	postnatal lethality, complete penetrance	J:7870
	weight loss	J:7870
Tcirg1oc/Tcirg1oc C57BL/6J-Vps33abf	abnormal bone ossification	J:28464
	absent teeth	J:28464
	circling	J:28464
	clubfoot	J:28464
	failure of bone resorption	J:28464
	premature death	J:28464
Tcirg1tm1.1Ywd/? involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	normal cellular phenotype	J:150327
Tcirg1tm1.1Ywd/Tcirg1tm1.1Ywd involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	no abnormal phenotype detected	J:150327
Tcirg1tm1.2Ywd/Tcirg1tm1.2Ywd involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N * SJL	abnormal macrophage physiology	J:150327
	absent teeth	J:150327
	decreased body size	J:150327
	premature death	J:150327
Tcirg1tm1Utku/Tcirg1tm1Utku involves: 129X1/SvJ * C57BL/6	abnormal immune serum protein physiology	J:92730
	abnormal immune system physiology	J:92730
	abnormal mesenteric lymph node morphology	J:92730
	abnormal peripheral lymph node morphology	J:92730
	abnormal Peyer's patch morphology	J:92730
	abnormal spleen B cell corona morphology	J:92730
	abnormal spleen morphology	J:92730
	abnormal spleen periarteriolar lymphoid sheath morphology	J:92730
	abnormal spleen red pulp morphology	J:92730
	abnormal spleen white pulp morphology	J:92730
	decreased B cell number	J:92730
	decreased body weight	J:92730
	decreased lymphocyte cell number	J:92730
	decreased spleen B cell follicle size	J:92730
	decreased T cell number	J:92730
	increased granulocyte number	J:92730
	increased IgG1 level	J:92730
	increased IgG2a level	J:92730
	increased IgM level	J:92730
	increased immunoglobulin level	J:92730
	increased spleen germinal center number	J:92730
	postnatal growth retardation	J:92730
	thymus atrophy	J:92730
Tcirg1tm1Ypl/Tcirg1tm1Ypl involves: 129S4/SvJae * C57BL/6J	abnormal bone marrow cavity morphology	J:58795
	abnormal bone mineralization	J:224711
	abnormal long bone hypertrophic chondrocyte zone	J:58795
	abnormal long bone metaphysis morphology	J:224711
	abnormal osteoclast physiology	J:58795
	absent compact bone	J:224711
	absent teeth	J:58795
	decreased body weight	J:58795
	decreased circulating calcium level	J:224711
	decreased compact bone thickness	J:58795
	decreased vitamin D level	J:224711
	failure of tooth eruption	J:58795
	increased bone mineral density	J:58795
	osteopetrosis	J:58795, J:224711
	premature death	J:58795
	rickets	J:224711
	short limbs	J:58795