80 phenotypes from 4 alleles in 5 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Fgfrl1tm1.1Ptew/Fgfrl1tm1.1Ptew B6.129-Fgfrl1tm1.1Ptew	abnormal appendicular skeleton morphology	J:149673
	abnormal brain morphology	J:149673
	abnormal cervical atlas morphology	J:149673
	abnormal cervical vertebrae morphology	J:149673
	abnormal diaphragm development	J:149673
	abnormal erythroblast number	J:149673
	abnormal foramen magnum morphology	J:149673
	abnormal forebrain development	J:149673
	abnormal hyoid bone morphology	J:149673
	abnormal neurocranium morphology	J:149673
	abnormal occipital bone morphology	J:149673
	abnormal pelvic girdle bone morphology	J:149673
	abnormal skeleton morphology	J:149673
	abnormal sphenoid bone morphology	J:149673
	abnormal spinal cord morphology	J:149673
	abnormal sternum ossification	J:149673
	abnormal vascular development	J:149673
	abnormal vertebrae morphology	J:149673
	abnormal vitelline vasculature morphology	J:149673
	anemia	J:149673
	axial skeleton hypoplasia	J:149673
	cardiac valve regurgitation	J:149673
	decreased birth body size	J:149673
	decreased body height	J:149673
	decreased erythrocyte cell number	J:149673
	decreased hematocrit	J:149673
	decreased hemoglobin content	J:149673
	decreased hyoid bone size	J:149673
	decreased long bone epiphyseal plate size	J:149673
	delayed cranial suture closure	J:149673
	disorganized placental labyrinth	J:149673
	domed cranium	J:149673
	enlarged brain ventricles	J:149673
	fetal growth retardation	J:149673
	fusion of basioccipital and basisphenoid bone	J:149673
	lethality throughout fetal growth and development, incomplete penetrance	J:149673
	mandible hypoplasia	J:149673
	midface hypoplasia	J:149673
	muscular ventricular septal defect	J:149673
	neonatal lethality, complete penetrance	J:149673
	pale placenta	J:149673
	pectus excavatum	J:149673
	perimembraneous ventricular septal defect	J:149673
	pulmonary valve stenosis	J:149673
	respiratory distress	J:149673
	short sternum	J:149673
	small basioccipital bone	J:149673
	small basisphenoid bone	J:149673
	small cricoid cartilage	J:149673
	small thoracic cage	J:149673
	small thoracic cavity	J:149673
	small thyroid cartilage	J:149673
	thick atrioventricular valve	J:149673
	thick semilunar valve	J:149673
	thin myocardium	J:149673
	thin neurocranium	J:149673
Fgfrl1tm1Ptew/Fgfrl1+ involves: 129 * C57BL/6J	no abnormal phenotype detected	J:149673
Fgfrl1tm1True/Fgfrl1+ B6.129S6-Fgfrl1tm1True	decreased renal glomerulus number	J:218981
Fgfrl1tm1True/Fgfrl1tm1True B6.129S6-Fgfrl1tm1True	abnormal diaphragm development	J:130254
	abnormal kidney development	J:153202
	abnormal metanephric mesenchyme morphology	J:153202
	abnormal metanephros morphology	J:153202
	abnormal nephrogenic mesenchyme morphogenesis	J:153202
	abnormal neurocranium morphology	J:218981
	absent kidney	J:153202
	absent metanephros	J:153202, J:218981
	absent nephron	J:153202
	cyanosis	J:130254
	decreased kidney cell proliferation	J:153202
	decreased length of long bones	J:218981
	diaphragmatic hernia	J:130254
	domed cranium	J:153203
	normal homeostasis/metabolism phenotype	J:218981
	impaired branching involved in ureteric bud morphogenesis	J:153202
	increased kidney apoptosis	J:153202
	muscle hypoplasia	J:130254
	neonatal lethality, complete penetrance	J:130254
	no spontaneous movement	J:130254
	respiratory distress	J:130254
	normal respiratory system phenotype	J:130254
	normal skeleton phenotype	J:130254
	small cranium	J:218981
	thin diaphragm muscle	J:130254, J:218981
Fgfrl1tm1True/Fgfrl1tm2.1True B6.Cg-Fgfrl1tm1True Fgfrl1tm2.1True	no abnormal phenotype detected	J:218981
Fgfrl1tm2.1True/Fgfrl1+ B6.Cg-Fgfrl1tm2.1True	decreased renal glomerulus number	J:218981
Fgfrl1tm2.1True/Fgfrl1tm2.1True B6.Cg-Fgfrl1tm2.1True	decreased renal glomerulus number	J:218981
	normal homeostasis/metabolism phenotype	J:218981
	normal mortality/aging	J:218981
	normal muscle phenotype	J:218981
	normal skeleton phenotype	J:218981