59 phenotypes from multigenic genotypes

Allelic Composition Genetic Background	Annotated Term	Reference
Ptprdtm1Yiw/Ptprd+ Ptprstm1Mtr/Ptprstm1Mtr B6.Cg-Ptprdtm1Yiw Ptprstm1Mtr	abnormal phrenic nerve morphology	J:109122
	decreased motor neuron number	J:109122
Ptprdtm1Yiw/Ptprdtm1Yiw Ptprstm1Mtr/Ptprs+ B6.Cg-Ptprdtm1Yiw Ptprstm1Mtr	abnormal phrenic nerve morphology	J:109122
Ptprdtm1Yiw/Ptprdtm1Yiw Ptprstm1Mtr/Ptprstm1Mtr B6.Cg-Ptprdtm1Yiw Ptprstm1Mtr	abnormal brown adipose tissue morphology	J:109122
	abnormal motor neuron morphology	J:109122
	abnormal phrenic nerve morphology	J:109122
	abnormal pulmonary alveolus morphology	J:109122
	axial skeleton hypoplasia	J:109122
	carpoptosis	J:109122
	centrally nucleated skeletal muscle fibers	J:109122
	decreased motor neuron number	J:109122
	hypaxial muscle hypoplasia	J:109122
	increased subcutaneous adipose tissue amount	J:109122
	kyphosis	J:109122
	neonatal lethality, complete penetrance	J:109122
	thin dermal layer	J:109122
	thin diaphragm muscle	J:109122
	translucent skin	J:109122
	underdeveloped hair follicles	J:109122
Ptprftm1Wjh/Ptprftm1Wjh Ptprstm1Mtr/Ptprstm1Mtr B6.Cg-Ptprftm1Wjh Ptprstm1Mtr	abnormal basisphenoid bone morphology	J:199299
	abnormal first pharyngeal arch morphology	J:199299
	abnormal frontal bone morphology	J:199299
	abnormal interparietal bone morphology	J:199299
	abnormal mandible morphology	J:199299
	abnormal mandibular symphysis morphology	J:199299
	abnormal Meckel's cartilage morphology	J:199299
	abnormal nasal capsule morphology	J:199299
	abnormal neurocranium morphology	J:199299
	abnormal palatal mesenchymal cell proliferation	J:199299
	abnormal palate bone morphology	J:199299
	abnormal parietal bone morphology	J:199299
	abnormal premaxilla morphology	J:199299
	abnormal retina neuronal layer morphology	J:149756
	abnormal tongue morphology	J:199299
	abnormal ureter development	J:149756
	abnormal ureter morphology	J:149756
	absent nasal capsule	J:199299
	absent palatine bone	J:199299
	absent pterygoid process	J:199299
	absent tongue	J:199299
	cleft secondary palate	J:149756, J:199299
	decreased tongue size	J:199299
	dilated ureter	J:149756
	disorganized retina inner nuclear layer	J:149756
	double ureter	J:149756
	duplex kidney	J:149756
	exencephaly	J:149756
	eyelids open at birth	J:149756
	glossoptosis	J:199299
	hydroureter	J:149756
	mandible hypoplasia	J:199299
	micrognathia	J:149756, J:199299
	oral atresia	J:199299
	palatal shelves fail to meet at midline	J:149756
	persistent hyaloid artery	J:149756
	premature death	J:149756
	short mandible	J:199299
	short premaxilla	J:199299
	normal skeleton phenotype	J:199299
	small mandible	J:199299
	ureterocele	J:149756
Ptprstm1Mtr/Ptprstm1Mtr Rtn4rtm1.1Pado/Rtn4rtm1.1Pado Rtn4rl1tm1.1Rojg/Rtn4rl1tm1.1Rojg involves: 129S/SvEvBrd * 129S4/SvJae	enhanced central nervous system regeneration	J:191258