42 phenotypes from 2 alleles in 1 genetic background

Allelic Composition Genetic Background	Annotated Term	Reference
Sp3tm1Sus/Sp3+ involves: 129P2/OlaHsd * C57BL/6	abnormal erythroid progenitor cell morphology	J:123073
	decreased body size	J:123073
Sp3tm1Sus/Sp3tm1Sus involves: 129P2/OlaHsd * C57BL/6	abnormal ameloblast morphology	J:60658
	abnormal B cell differentiation	J:84837
	abnormal basicranium morphology	J:70829
	abnormal basisphenoid bone morphology	J:70829
	abnormal bone mineralization	J:70829
	abnormal cervical atlas morphology	J:70829
	abnormal cranium morphology	J:70829
	abnormal dentin development	J:60658
	abnormal enamel development	J:60658
	abnormal erythropoiesis	J:84837
	abnormal frontal bone morphology	J:70829
	abnormal interparietal bone morphology	J:70829
	abnormal metacarpal bone morphology	J:70829
	abnormal metatarsal bone morphology	J:70829
	abnormal nasal bone morphology	J:70829
	abnormal osteoblast differentiation	J:70829
	abnormal parietal bone morphology	J:70829
	abnormal phalanx morphology	J:70829
	abnormal placenta labyrinth morphology	J:123073
	abnormal presphenoid bone morphology	J:70829
	abnormal pulmonary alveolus morphology	J:60658
	abnormal sagittal suture morphology	J:70829
	abnormal sternum ossification	J:70829
	abnormal supraoccipital bone morphology	J:70829
	abnormal tooth development	J:60658
	abnormal trophoblast glycogen cell morphology	J:123073
	abnormal vertebral body morphology	J:70829
	abnormal xiphoid process morphology	J:70829
	decreased birth body size	J:60658
	decreased CD4-positive, alpha-beta T cell number	J:84837
	decreased spongiotrophoblast cell number	J:123073
	decreased spongiotrophoblast size	J:123073
	delayed bone ossification	J:70829
	delayed endochondral bone ossification	J:70829
	delayed intramembranous bone ossification	J:70829
	liver hypoplasia	J:84837
	neonatal lethality, complete penetrance	J:60658
	respiratory failure	J:60658
	small thymus	J:84837
Sp3tm2.1Sus/Sp3tm2.1Sus involves: 129P2/OlaHsd * C57BL/6	abnormal DNA methylation	J:167521