29 phenotypes from 4 alleles in 4 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Lrp8tm1Her/Lrp8tm1Her involves: 129S6/SvEvTac	abnormal brain development	J:55691
	abnormal cell death	J:117956
	abnormal cerebral cortex morphology	J:105699
	abnormal contextual conditioning behavior	J:55691
	abnormal dentate gyrus morphology	J:55691, J:105699
	abnormal hippocampus layer morphology	J:105699
	abnormal neuronal migration	J:117956
	abnormal Purkinje cell morphology	J:55691
	abnormal spatial learning	J:100988
	abnormal sperm flagellum morphology	J:84102
	abnormal sperm midpiece morphology	J:84102
	abnormal sperm mitochondrial sheath morphology	J:84102
	abnormal sperm physiology	J:84102
	abnormal spermatogenesis	J:84102
	asthenozoospermia	J:84102
	coiled sperm flagellum	J:84102
	hairpin sperm flagellum	J:84102
	kinked sperm flagellum	J:84102
	male infertility	J:55691, J:84102
	reduced cerebellar foliation	J:55691
	small cerebellum	J:55691
Lrp8tm1Her/Lrp8tm1Her involves: 129S6/SvEvTac * C57BL/6	abnormal cerebral cortex morphology	J:129338
	abnormal hippocampus pyramidal cell layer	J:129338
Lrp8tm1Her/Lrp8tm1Her involves: 129S6/SvEvTac * C57BL/6J	abnormal lateral ventricle morphology	J:121846
	abnormal postnatal subventricular zone morphology	J:121846
	abnormal rostral migratory stream morphology	J:121846
Lrp8tm2.1Her/Lrp8tm2.1Her involves: 129S6/SvEvTac	abnormal cell death	J:117956
	decreased motor neuron number	J:117956
	neuron degeneration	J:117956
Lrp8tm2.1Her/Lrp8tm2.1Her involves: 129S6/SvEvTac * C57BL/6J	no abnormal phenotype detected	J:100988
Lrp8tm3Her/Lrp8tm3Her involves: 129S6/SvEvTac * C57BL/6J	abnormal contextual conditioning behavior	J:100988
	abnormal spatial learning	J:100988
	reduced long-term potentiation	J:100988
Lrp8tm5Her/Lrp8tm5Her Not Specified	abnormal neuronal migration	J:117956
	neuron degeneration	J:117956