39 phenotypes from 3 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Ranbp1Gt(S17-6E1)1.1Sor/Ranbp1Gt(S17-6E1)1.1Sor B6.129S4(129S6)-Ranbp1Gt(S17-6E1)1.1Sor	abnormal cell cycle	J:235630
	abnormal cortical intermediate zone morphology	J:235630
	abnormal embryo morphology	J:235630
	abnormal embryonic/fetal subventricular zone morphology	J:235630
	abnormal eye distance/ position	J:235630
	abnormal first pharyngeal arch morphology	J:235630
	abnormal forebrain development	J:235630
	abnormal neural tube closure	J:235630
	abnormal neuron differentiation	J:235630
	abnormal neuronal precursor proliferation	J:235630
	abnormal pharyngeal arch morphology	J:235630
	abnormal second pharyngeal arch morphology	J:235630
	abnormal telencephalon morphology	J:235630
	coloboma	J:235630
	decreased brain size	J:235630
	decreased embryo size	J:235630
	decreased neuron number	J:235630
	exencephaly	J:235630
	lethality during fetal growth through weaning, complete penetrance	J:235630
	microcephaly	J:235630
	microphthalmia	J:235630
	small olfactory bulb	J:235630
	thin cerebral cortex	J:235630
	thin cortical plate	J:235630
Ranbp1tm1b(KOMP)Wtsi/Ranbp1tm1b(KOMP)Wtsi C57BL/6N-Ranbp1tm1b(KOMP)Wtsi/Tcp	abnormal craniofacial morphology	J:211773
	abnormal embryo size	J:211773
	abnormal forebrain morphology	J:211773
	abnormal hindbrain morphology	J:211773
	abnormal midbrain morphology	J:211773
	abnormal neural tube closure	J:211773
	abnormal placenta size	J:211773
	edema	J:211773
	preweaning lethality, complete penetrance	J:211773
Ranbp1tm1Yyo/Ranbp1tm1Yyo involves: 129S2/SvPas * C57BL/6	abnormal male germ cell apoptosis	J:170335
	abnormal spermatogenesis	J:170335
	azoospermia	J:170335
	decreased body weight	J:170335
	male infertility	J:170335
	postnatal growth retardation	J:170335
	normal reproductive system phenotype	J:170335