25 phenotypes from 3 alleles in 4 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Myrfem1(IMPC)Bay/Myrf+ C57BL/6N-Myrfem1(IMPC)Bay/BayMmucd	abnormal embryo size	J:211773
	embryonic growth retardation	J:211773
	increased cornea thickness	J:211773
Myrfem1(IMPC)Bay/Myrfem1(IMPC)Bay C57BL/6N-Myrfem1(IMPC)Bay/BayMmucd	abnormal embryo size	J:211773
	abnormal embryo turning	J:211773
	embryonic growth retardation	J:211773
	embryonic lethality prior to tooth bud stage	J:211773
	preweaning lethality, complete penetrance	J:211773
Myrftm1Barr/Myrf+ Tg(rx3-icre)1Mjam/0 involves: 129P2/OlaHsd * C57BL/6J	retina degeneration	J:275842
	retina pigment epithelium atrophy	J:275842
Myrftm1Barr/Myrftm1.1Barr Tg(rx3-icre)1Mjam/0 involves: 129P2/OlaHsd * C57BL/6J	abnormal retina pigmentation	J:275842
Myrftm1Barr/Myrftm1Barr Cnptm1(cre)Kan/Cnp+ involves: 129P2/OlaHsd * 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * C57BL/6	abnormal myelination	J:150563
	abnormal oligodendrocyte morphology	J:150563
	abnormal spinal cord morphology	J:150563
	postnatal lethality, complete penetrance	J:150563
	seizures	J:150563
	tremors	J:150563
Myrftm1Barr/Myrftm1Barr Olig2tm2(TVA,cre)Rth/Olig2+ involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6	abnormal myelination	J:150563
	abnormal optic nerve morphology	J:150563
	abnormal spinal cord morphology	J:150563
	ataxia	J:150563
	normal nervous system phenotype	J:150563
	postnatal lethality, complete penetrance	J:150563
	seizures	J:150563
	tremors	J:150563
Myrftm1Barr/Myrftm1Barr Tg(rx3-icre)1Mjam/0 involves: 129P2/OlaHsd * C57BL/6J	abnormal cone electrophysiology	J:275842
	abnormal retina pigmentation	J:275842
	abnormal rod electrophysiology	J:275842
	decreased retina cone cell number	J:275842
	decreased total retina thickness	J:275842
	retina degeneration	J:275842
	retina pigment epithelium atrophy	J:275842
	short photoreceptor inner segment	J:275842
	short photoreceptor outer segment	J:275842
	thin retina outer nuclear layer	J:275842