68 phenotypes from 4 alleles in 5 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Rspo2ftls/Rspo2+ involves: FVB/N	cleft secondary palate	J:83881
	decreased ovulation rate	J:83881
	delayed kidney development	J:83881
	ovary cyst	J:83881
	reduced female fertility	J:83881
	single kidney	J:83881
Rspo2ftls/Rspo2ftls involves: FVB/N	abnormal forelimb morphology	J:83881
	abnormal hindlimb morphology	J:83881
	abnormal kidney development	J:83881
	abnormal phalanx morphology	J:83881
	absence of all nails	J:83881
	absent fibula	J:83881
	absent radius	J:83881
	cleft secondary palate	J:83881
	perinatal lethality, complete penetrance	J:83881
	short tibia	J:83881
	single kidney	J:83881
Rspo2ftls/Rspo2ftls Not Specified	abnormal autopod morphology	J:188812
	abnormal autopod rotation	J:188812
	abnormal digit morphology	J:188812
	abnormal forelimb morphology	J:188812
	abnormal hindlimb morphology	J:188812
	abnormal limb morphology	J:188812
	absent fibula	J:188812
	absent radius	J:188812
	absent tibia	J:188812
	short hindlimb	J:188812
Rspo2tm1Hoka/Rspo2tm1Hoka involves: C57BL/6 * CBA	abnormal apical ectodermal ridge morphology	J:133600
	abnormal autopod morphology	J:133600
	abnormal digit morphology	J:133600
	abnormal forelimb morphology	J:133600
	abnormal forelimb zeugopod morphology	J:133600
	abnormal hindlimb morphology	J:133600
	abnormal limb development	J:133600
	abnormal phalanx morphology	J:133600
	absent fibula	J:133600
	perinatal lethality, complete penetrance	J:133600
Rspo2tm1Nuv/Rspo2+ involves: 129 * C57BL/6	reduced female fertility	J:126341
Rspo2tm1Nuv/Rspo2tm1Nuv involves: 129 * C57BL/6	abnormal apical ectodermal ridge morphology	J:126341
	abnormal bone ossification	J:126341
	abnormal digestive system development	J:171482
	abnormal limb development	J:126341
	abnormal lung vasculature morphology	J:126341
	abnormal mandibular angle morphology	J:171482
	abnormal maxillary shelf morphology	J:171482
	abnormal maxillary zygomatic process morphology	J:171482
	abnormal palatal shelf fusion at midline	J:171482
	abnormal phalanx morphology	J:126341
	abnormal pharyngeal arch mesenchyme morphology	J:171482
	abnormal tooth development	J:171482
	absence of all nails	J:126341
	absent kidney	J:126341
	absent mandibular coronoid process	J:171482
	brachyphalangia	J:126341
	cleft palate	J:126341
	cleft secondary palate	J:171482
	decreased tongue size	J:171482
	decreased tympanic ring size	J:171482
	delayed palatal shelf elevation	J:171482
	growth retardation of incisors	J:171482
	perinatal lethality, complete penetrance	J:126341
	pulmonary hypoplasia	J:126341
	short fibula	J:126341
	short mandible	J:171482
	short Meckel's cartilage	J:171482
	short metatarsal bones	J:126341
	small mandible	J:171482
	small mandibular condyloid process	J:171482
	small maxilla	J:171482
	syndactyly	J:126341
Rspo2tm1Suda/Rspo2tm1Suda B6.Cg-Rspo2tm1Suda	abnormal autopod morphology	J:146829
	abnormal laryngeal cartilage morphology	J:146829
	abnormal lung morphology	J:146829
	abnormal maxilla morphology	J:146829
	abnormal nail morphology	J:146829
	abnormal pulmonary alveolus morphology	J:146829
	abnormal temporal bone squamous part morphology	J:146829
	abnormal tracheal cartilage morphology	J:146829
	abnormal zygomatic bone morphology	J:146829
	absent mandibular coronoid process	J:146829
	arytenoid and cricoid cartilage fusion	J:146829
	cleft secondary palate	J:146829
	cleft upper lip	J:146829
	cyanosis	J:146829
	decreased palatine bone horizontal plate size	J:146829
	hindlimb oligodactyly	J:146829
	lung hemorrhage	J:146829
	maxillary shelf hypoplasia	J:146829
	neonatal lethality, complete penetrance	J:146829
	palatal shelves fail to meet at midline	J:146829
	pulmonary hypoplasia	J:146829
	respiratory failure	J:146829