39 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Pxdnem1(IMPC)J/Pxdnem1(IMPC)J C57BL/6NJ-Pxdnem1(IMPC)J/Mmjax	decreased thigmotaxis	J:211773
	hyperactivity	J:211773
	increased vertical activity	J:211773
	preweaning lethality, incomplete penetrance	J:211773
Pxdnmhdakta048/Pxdnmhdakta048 involves: C3HeB/FeJ * C57BL/6J	abnormal anterior eye segment morphology	J:213336
	abnormal corneal stroma morphology	J:213336
	abnormal extracellular matrix morphology	J:213336
	abnormal eye anterior chamber morphology	J:213336
	abnormal eye posterior chamber morphology	J:213336
	abnormal iridocorneal angle	J:213336
	abnormal iris morphology	J:213336
	abnormal lens development	J:213336
	abnormal lens epithelium morphology	J:213336
	abnormal lens fiber morphology	J:213336
	abnormal optic nerve morphology	J:213336
	abnormal retina inner limiting membrane morphology	J:213336
	abnormal retina morphology	J:213336
	absent eye anterior chamber	J:213336
	belly spot	J:213336
	ciliary body hypoplasia	J:213336
	corneal opacity	J:213336
	corneal-lenticular stalk	J:213336
	decreased cell proliferation	J:213336
	decreased corneal epithelium thickness	J:213336
	decreased eye anterior chamber depth	J:213336
	decreased retina ganglion cell number	J:213336
	disorganized secondary lens fibers	J:213336
	eye inflammation	J:213336
	fused cornea and lens	J:213336
	increased corneal stroma thickness	J:213336
	iris hypoplasia	J:213336
	kinked tail	J:213336
	microphthalmia	J:213336
	optic nerve hypoplasia	J:213336
	retina fold	J:213336
	retina gliosis	J:213336
	ruptured lens capsule	J:213336
	small lens	J:213336
	vitreous body deposition	J:213336