57 phenotypes from 4 alleles in 6 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Col10a1tm1.1Rpbh/Col10a1+ involves: 129 * C57BL/6	increased width of hypertrophic chondrocyte zone	J:154052
	short femur	J:154052
Col10a1tm1.1Rpbh/Col10a1tm1.1Rpbh involves: 129S1/Sv * 129X1/SvJ * C57BL/6	abnormal cell morphology	J:154052
	abnormal pelvic girdle bone morphology	J:154052
	decreased osteoclast cell number	J:154052
	disproportionate dwarf	J:154052
	increased endoplasmic reticulum stress	J:154052
	increased width of hypertrophic chondrocyte zone	J:154052
	short femur	J:154052
	slow postnatal weight gain	J:154052
Col10a1tm1Bhr/Col10a1tm1Bhr involves: 129S7/SvEvBrd * C57BL/6	abnormal bone marrow morphology	J:62230
	abnormal cervical axis morphology	J:20879
	abnormal long bone epiphyseal plate morphology	J:62230
	abnormal long bone epiphyseal plate proliferative zone	J:62230
	abnormal proerythroblast morphology	J:62230
	abnormal spleen morphology	J:62230
	abnormal tooth development	J:62230
	abnormal trabecular bone morphology	J:62230
	absent lymph nodes	J:62230
	cachexia	J:62230
	decreased B cell number	J:62230
	decreased body weight	J:62230
	decreased double-positive T cell number	J:62230
	decreased spleen red pulp amount	J:62230
	decreased spleen weight	J:62230
	decreased thymocyte number	J:62230
	decreased thymus weight	J:62230
	hydrocephaly	J:62230
	increased CD4-positive, alpha-beta T cell number	J:62230
	increased double-negative T cell number	J:62230
	increased single-positive T cell number	J:62230
	kyphosis	J:62230
	lethargy	J:62230
	lordosis	J:62230
	postnatal lethality, incomplete penetrance	J:62230
	premature death	J:62230
	normal skeleton phenotype	J:20879
	small spleen	J:62230
	small thymus	J:62230
	spleen hypoplasia	J:62230
	thymus hypoplasia	J:62230
Col10a1tm1Ksec/Col10a1tm1Ksec 129/Sv-Col10a1tm1Ksec	abnormal long bone epiphyseal plate morphology	J:38124
	abnormal trabecular bone morphology	J:38124
	coxa vara	J:38124
	decreased bone mineral content	J:38124
Col10a1tm1Ksec/Col10a1tm1Ksec involves: 129S/SvEv * C57BL/6	abnormal cartilage morphology	J:38124
	abnormal femur morphology	J:193886
	abnormal long bone epiphyseal plate morphology	J:38124
	abnormal T-helper 2 cell differentiation	J:193886
	abnormal trabecular bone morphology	J:38124
	coxa vara	J:38124
	decreased bone mass	J:38124
	decreased bone mineral content	J:193886
	decreased bone mineral density of femur	J:193886
	decreased dendritic cell number	J:193886
	decreased interleukin-2 secretion	J:193886
	decreased interleukin-4 secretion	J:193886
	decreased interleukin-10 secretion	J:193886
	decreased interleukin-17 secretion	J:193886
	increased B cell number	J:193886
	increased interleukin-4 secretion	J:193886
	increased T-helper cell number	J:193886
	increased width of hypertrophic chondrocyte zone	J:193886
Col10a1tm2.1Rpbh/Col10a1+ involves: C57BL/6NTac	abnormal chondrocyte differentiation	J:267200
	abnormal endochondral bone ossification	J:267200
	abnormal pelvic girdle bone morphology	J:267200
	decreased body weight	J:267200
	disproportionate dwarf	J:267200
	increased endoplasmic reticulum stress	J:267200
	increased width of hypertrophic chondrocyte zone	J:267200
	postnatal growth retardation	J:267200
Col10a1tm2.1Rpbh/Col10a1tm2.1Rpbh involves: C57BL/6NTac	abnormal chondrocyte differentiation	J:267200
	abnormal endochondral bone ossification	J:267200
	abnormal pelvic girdle bone morphology	J:267200
	decreased body weight	J:267200
	disproportionate dwarf	J:267200
	increased endoplasmic reticulum stress	J:267200
	increased width of hypertrophic chondrocyte zone	J:267200
	postnatal growth retardation	J:267200