60 phenotypes from 6 alleles in 6 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Med23em1(IMPC)Wtsi/Med23+ C57BL/6N-Med23em1(IMPC)Wtsi/Wtsi	decreased bone mineral content	J:211773
	decreased circulating fructosamine level	J:211773
	increased circulating HDL cholesterol level	J:211773
	increased lean body mass	J:211773
	increased red blood cell distribution width	J:211773
Med23em1(IMPC)Wtsi/Med23em1(IMPC)Wtsi C57BL/6N-Med23em1(IMPC)Wtsi/Wtsi	abnormal chorion morphology	J:261316
	abnormal placenta morphology	J:261316
	abnormal trophoblast giant cell morphology	J:261316
	abnormal trophoblast layer morphology	J:261316
	lethality throughout fetal growth and development, complete penetrance	J:261316
	preweaning lethality, complete penetrance	J:211773
Med23snouty/Med23snouty involves: 129S1/Sv * C57BL/6 * FVB/NJ	abnormal blood vessel morphology	J:171522
	abnormal nervous system development	J:171522
	abnormal trigeminal ganglion morphology	J:171522
	absent second pharyngeal arch	J:171522
	decreased embryo size	J:171522
	embryonic lethality during organogenesis, complete penetrance	J:171522
	impaired cranial neural crest cell differentiation	J:171522
	second pharyngeal arch hypoplasia	J:171522
	small frontonasal prominence	J:171522
Med23tm1.1Pkb/Med23tm1.1Pkb 129S(B6)-Med23tm1.1Pkb/J	no abnormal phenotype detected	J:101977
Med23tm1Berk/Med23tm1Berk involves: 129S4/SvJae	abnormal nervous system development	J:188551
	abnormal vascular development	J:188551
	embryonic growth retardation	J:188551
	embryonic lethality during organogenesis, complete penetrance	J:188551
Med23tm1c(KOMP)Wtsi/Med23tm1c(KOMP)Wtsi H2az2Tg(Wnt1-cre)11Rth/H2az2+ involves: C57BL/6J * C57BL/6N * CBA/J	abnormal cranial cartilage development	J:304767
	abnormal craniofacial morphology	J:304767
	abnormal cranium morphology	J:304767
	abnormal first pharyngeal arch morphology	J:304767
	abnormal frontonasal prominence morphology	J:304767
	abnormal Meckel's cartilage morphology	J:304767
	abnormal nasal cartilage morphology	J:304767
	abnormal palatal mesenchymal cell proliferation	J:304767
	abnormal secondary palate development	J:304767
	abnormal suckling behavior	J:304767
	abnormal tongue morphology	J:304767
	abnormal tooth development	J:304767
	abnormal tympanic ring morphology	J:304767
	absent mandibular symphysis	J:304767
	absent palatine bone	J:304767
	normal cellular phenotype	J:304767
	cleft palate	J:304767
	normal embryo phenotype	J:304767
	failure of palatal shelf elevation	J:304767
	frontal bone hypoplasia	J:304767
	glossoptosis	J:304767
	growth retardation of incisors	J:304767
	growth retardation of molars	J:304767
	mandible hypoplasia	J:304767
	mandibular condyloid process hypoplasia	J:304767
	Meckel's cartilage hypoplasia	J:304767
	micrognathia	J:304767
	nasal cartilage hypoplasia	J:304767
	neonatal lethality, complete penetrance	J:304767
	normal nervous system phenotype	J:304767
	palatal shelf hypoplasia	J:304767
	palatal shelves fail to meet at midline	J:304767
	respiratory distress	J:304767
	small lower incisors	J:304767
	small mandible	J:304767
	temporal bone hypoplasia	J:304767
Med23tm1Gwan/Med23tm1Gwan involves: 129 * C57BL/6	abnormal cell differentiation	J:187746