33 phenotypes from 3 alleles in 4 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Rbl2tm1b(EUCOMM)Hmgu/Rbl2+ C57BL/6N-Rbl2tm1b(EUCOMM)Hmgu/J	abnormal retina morphology	J:211773
	increased circulating cholesterol level	J:211773
	increased circulating HDL cholesterol level	J:211773
Rbl2tm1b(EUCOMM)Hmgu/Rbl2tm1b(EUCOMM)Hmgu C57BL/6N-Rbl2tm1b(EUCOMM)Hmgu/J	preweaning lethality, incomplete penetrance	J:211773
Rbl2tm1Mru/Rbl2tm1Mru involves: 129S4/SvJae * BALB/cJ	abnormal cell proliferation	J:50516
	abnormal developmental patterning	J:50516
	abnormal floor plate morphology	J:50516
	abnormal heart morphology	J:50516
	abnormal myotome development	J:50516
	abnormal neuron differentiation	J:50516
	absent floor plate	J:50516
	absent hindlimb buds	J:50516
	absent notochord	J:50516
	normal cardiovascular system phenotype	J:50516
	normal cellular phenotype	J:50516
	decreased embryo size	J:50516
	normal embryo phenotype	J:50516
	embryonic growth arrest	J:50516
	embryonic lethality during organogenesis, complete penetrance	J:50516
	enlarged heart	J:50516
	failure of heart looping	J:50516
	failure of initiation of embryo turning	J:50516
	normal growth/size/body region phenotype	J:50516
	incomplete somite formation	J:50516
	increased apoptosis	J:50516
	increased neuron apoptosis	J:50516
	normal limbs/digits/tail phenotype	J:50516
	normal mortality/aging	J:50516
	normal muscle phenotype	J:50516
	normal nervous system phenotype	J:50516
	thin myocardium	J:50516
Rbl2tm1Mru/Rbl2tm1Mru involves: 129S4/SvJae * BALB/cJ * C57BL/6J	no abnormal phenotype detected	J:50516
Rbl2tm1Tyj/Rbl2+ involves: 129S2/SvPas * C57BL/6	no abnormal phenotype detected	J:34725
Rbl2tm1Tyj/Rbl2tm1Tyj involves: 129S2/SvPas * C57BL/6	normal cellular phenotype	J:34725
	normal integument phenotype	J:82802
	no abnormal phenotype detected	J:34725