Pax9 Phenotype Annotations - Multigenic Genotypes

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Pax9
paired box 9
MGI:97493

39 phenotypes from multigenic genotypes

Allelic Composition Genetic Background	Annotated Term	Reference
Isl1^tm1(cre)Sev/Isl1⁺ Msx1^tm1Rilm/Msx1⁺ Pax9^tm1Rbal/Pax9^tm1.1Hpt involves: 129 * CD-1	aberrant origin of the right subclavian artery	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 superior horn of thyroid cartilage morphology	J:311535
	craniofacial phenotype	J:311535
	neonatal lethality, complete penetrance	J:311535
	preaxial polydactyly	J:311535
Msx1^tm1Rilm/Msx1⁺ Pax9^tm1Rbal/Pax9⁺ involves: 129 * CD-1	decreased tooth number	J:311535
Msx1^tm1Rilm/Msx1⁺ Pax9^tm1Rbal/Pax9^tm1Rbal involves: 129 * CD-1	aberrant origin of the right subclavian artery	J:311535
	abnormal aorta 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 second pharyngeal arch artery morphology	J:311535
	abnormal third pharyngeal arch artery morphology	J:311535
	cleft secondary 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
	interrupted aortic arch	J:311535
	neonatal lethality	J:311535
	preaxial polydactyly	J:311535
	third pharyngeal arch artery hypoplasia	J:311535
	thymus hypoplasia	J:311535
Msx1^tm1Rilm/Msx1^tm1Rilm Pax9^tm1Rbal/Pax9⁺ involves: 129 * CD-1	cleft palate	J:311535
Msx1^tm1Rilm/Msx1^tm1Rilm Pax9^tm1Rbal/Pax9^tm1Rbal involves: 129 * CD-1	aberrant origin of the right subclavian artery	J:311535
	abnormal pharyngeal arch artery morphology	J:311535
	double outlet right ventricle	J:311535
	interrupted aortic arch, type b	J:311535
	normal limbs/digits/tail phenotype	J:311535
Osr2^tm1Jian/Osr2^tm1Jian Pax9^{tm1.1(Osr2)Jian}/Pax9⁺ involves: 129S1/Sv * C57BL/6J * FVB/N	abnormal tooth development	J:173121
	cleft secondary palate	J:173121
Osr2^tm1Jian/Osr2^tm1Jian Pax9^{tm1.2(Osr2)Jian}/Pax9⁺ involves: 129S1/Sv * 129S4/SvJaeSor * C57BL/6J * FVB/N	cleft secondary palate	J:173121
	normal craniofacial phenotype	J:173121
Pax9^{tm1(Osr2)Jian}/Pax9^{tm1(Osr2)Jian} involves: 129S1/Sv * C57BL/6J	abnormal lower incisor morphology	J:173121
Pax9^{tm1.1(Osr2)Jian}/Pax9^{tm1.1(Osr2)Jian} involves: 129S1/Sv * C57BL/6J * FVB/N	abnormal craniofacial bone morphology	J:173121
	abnormal mandible morphology	J:173121
	abnormal palatal shelf morphology	J:173121
	absent mandibular coronoid process	J:173121
	arrest of tooth development	J:173121
	cleft secondary palate	J:173121
	decreased tympanic ring size	J:173121
	neonatal lethality, complete penetrance	J:173121
	palatal shelves fail to meet at midline	J:173121
	preaxial polydactyly	J:173121
	small mandible	J:173121

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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