35 phenotypes from 3 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
2700049A03Riktm1.1Arte/2700049A03Riktm1.1Arte Tg(Prrx1-cre)1Cjt/0 involves: C57BL/6J * C57BL/6NTac * SJL/J	abnormal carpal bone morphology	J:175541
	abnormal cilium morphology	J:175541
	abnormal digit development	J:175541
	abnormal digit morphology	J:175541
	abnormal embryonic autopod plate morphology	J:175541
	abnormal endochondral bone ossification	J:175541
	abnormal limb mesenchyme morphology	J:175541
	abnormal long bone epiphyseal plate morphology	J:175541
	abnormal skeleton development	J:175541
	brachydactyly	J:175541
	decreased fibroblast cell migration	J:175541
	decreased length of long bones	J:175541
	polydactyly	J:175541
	polysyndactyly	J:175541
	short femur	J:175541
	short fibula	J:175541
	short humerus	J:175541
	short limbs	J:175541
	short radius	J:175541
	short scapula	J:175541
	short tibia	J:175541
	short ulna	J:175541
2700049A03Riktm1.2Arte/2700049A03Riktm1.2Arte either: (involves: C57BL/6NTac) or (involves: C57BL/6NTac * CD-1)	abnormal centrosome morphology	J:175541
	abnormal direction of heart looping	J:175541
	abnormal lateral nasal prominence morphology	J:175541
	abnormal left-right axis patterning	J:175541
	abnormal medial nasal prominence morphology	J:175541
	abnormal neural tube morphology	J:175541
	absent embryonic cilia	J:175541
	embryonic growth arrest	J:175541
	embryonic lethality during organogenesis, complete penetrance	J:175541
	hemorrhage	J:175541
	narrow head	J:175541
	pericardial edema	J:175541
2700049A03Riktm1Blnw/2700049A03Riktm1Blnw Not Specified	abnormal cell morphology	J:220629
	abnormal cilium morphology	J:220629