84 phenotypes from 5 alleles in 10 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Isl1tm1(cre)Sev/Isl1+ Pax9tm1Rbal/Pax9tm1.1Hpt involves: 129 * C57BL/6J	aberrant origin of the right subclavian artery	J:311535
	abnormal common carotid artery morphology	J:311535
	normal craniofacial phenotype	J:311535
	double outlet right ventricle	J:311535
	ectopic thymus	J:311535
	interrupted aortic arch	J:311535
	preaxial polydactyly	J:311535
	thymus hypoplasia	J:311535
	ventricular septal defect	J:311535
Pax9tm1.1Hpt/Pax9tm1.1Hpt involves: 129S2/SvPas * C57BL/6 * SJL	no abnormal phenotype detected	J:125026
Pax9tm1.1Hpt/Pax9tm1.1Hpt H2az2Tg(Wnt1-cre)11Rth/H2az2+ involves: 129S2/SvPas * C57BL/6 * CBA * SJL	abnormal maxillary shelf morphology	J:125026
	abnormal palatine bone horizontal plate morphology	J:125026
	absent alveolar process	J:125026
	absent mandibular coronoid process	J:125026
	absent premaxilla	J:125026
	absent teeth	J:125026
	aphagia	J:125026
	arrest of tooth development	J:125026
	cleft secondary palate	J:125026
	failure of palatal shelf elevation	J:125026
	neonatal lethality, complete penetrance	J:125026
Pax9tm1.1Hpt/Pax9tm1.1Hpt Tg(Pgk1-cre)1Lni/? involves: 129S2/SvPas * BALB/c * C57BL/6 * SJL	abnormal maxillary shelf morphology	J:125026
	abnormal palatine bone horizontal plate morphology	J:125026
	abnormal thymus lobule morphology	J:125026
	abnormal tympanic ring morphology	J:125026
	absent mandibular coronoid process	J:125026
	absent parathyroid glands	J:125026
	absent premaxilla	J:125026
	absent teeth	J:125026
	aphagia	J:125026
	cleft secondary palate	J:125026
	neonatal lethality, complete penetrance	J:125026
	polydactyly	J:125026
Pax9tm1.2(Osr2)Jian/Pax9+ involves: 129S1/Sv * 129S4/SvJaeSor * C57BL/6J * FVB/N	normal craniofacial phenotype	J:173121
Pax9tm1.3(Osr2)Jian/Pax9tm1.3(Osr2)Jian involves: 129S1/Sv * C57BL/6J	normal mortality/aging	J:173121
	normal reproductive system phenotype	J:173121
Pax9tm1Hpt/Pax9tm1Hpt involves: 129S2/SvPas * C57BL/6	abnormal dentin morphology	J:104121
	abnormal molar morphology	J:104121
	abnormal tooth attrition	J:104121
	abnormal tooth development	J:104121
	abnormal tooth morphology	J:104121
	absent lower incisors	J:104121
	decreased molar number	J:104121
	decreased tooth number	J:104121
	normal endocrine/exocrine gland phenotype	J:104121
	failure of tooth eruption	J:104121
Pax9tm1Hpt/Pax9tm1Rbal involves: 129 * C57BL/6 * CD-1	abnormal ameloblast morphology	J:104121
	abnormal dentin development	J:104121
	abnormal molar morphology	J:104121
	abnormal tooth attrition	J:104121
	abnormal tooth development	J:104121
	absent enamel	J:104121
	absent lower incisors	J:104121
	arrest of tooth development	J:104121
	decreased body size	J:104121
	decreased molar number	J:104121
	decreased tooth number	J:104121
	normal endocrine/exocrine gland phenotype	J:104121
	failure of tooth eruption	J:104121
	growth retardation of molars	J:104121
	postnatal lethality, incomplete penetrance	J:104121
Pax9tm1Rbal/Pax9tm1Rbal involves: 129S1/Sv * 129X1/SvJ * C57BL/6	abnormal autopod muscle morphology	J:49857
	abnormal cranium morphology	J:49857
	abnormal laryngeal cartilage morphology	J:49857
	abnormal limb development	J:49857
	abnormal mandible morphology	J:49857
	abnormal palatal shelf elevation	J:49857
	abnormal palatal shelf morphology	J:49857
	abnormal pharyngeal pouch morphology	J:49857
	abnormal pterygoid process morphology	J:49857
	abnormal Reichert's cartilage morphology	J:49857
	abnormal tendon morphology	J:49857
	abnormal thyroid cartilage morphology	J:49857
	absent alveolar process	J:49857
	absent incisors	J:49857
	absent mandibular coronoid process	J:49857
	absent maxillary shelf	J:49857
	absent molars	J:49857
	absent palatine bone horizontal plate	J:49857
	absent parathyroid glands	J:49857
	absent Reichert cartilage	J:49857
	absent teeth	J:49857
	absent ultimobranchial body	J:49857
	arrest of tooth development	J:49857
	athymia	J:49857
	cleft secondary palate	J:49857
	decreased tympanic ring size	J:49857
	distended abdomen	J:49857
	neonatal lethality, complete penetrance	J:49857
	polydactyly	J:49857
	polysyndactyly	J:49857
	respiratory distress	J:49857
Pax9tm1Rbal/Pax9tm1Rbal involves: 129S1/Sv * 129X1/SvJ * CD-1	aberrant origin of the right subclavian artery	J:311535
	abnormal aortic arch morphology	J:311535
	abnormal common carotid artery morphology	J:311535
	abnormal first pharyngeal arch artery morphology	J:311535
	abnormal fourth pharyngeal arch artery morphology	J:311535
	abnormal hyoid bone greater horn morphology	J:311535
	abnormal hyoid bone lesser horn morphology	J:311535
	abnormal hyoid bone morphology	J:311535
	abnormal inferior horn of thyroid cartilage morphology	J:311535
	abnormal second pharyngeal arch artery morphology	J:311535
	abnormal superior horn of thyroid cartilage morphology	J:311535
	abnormal third pharyngeal arch artery morphology	J:311535
	absent fourth pharyngeal arch artery	J:311535
	absent third pharyngeal arch artery	J:311535
	cleft palate	J:311535
	decreased neural crest cell number	J:311535
	double outlet right ventricle	J:311535
	ectopic thymus	J:311535
	fourth pharyngeal arch artery hypoplasia	J:311535
	fused tracheal cartilage rings	J:311535
	interrupted aortic arch	J:311535
	neonatal lethality	J:311535
	preaxial polydactyly	J:311535
	third pharyngeal arch artery hypoplasia	J:311535
	thymus hypoplasia	J:311535
	ventricular septal defect	J:311535