45 phenotypes from 1 allele in 1 genetic background

Allelic Composition Genetic Background	Annotated Term	Reference
Rpl24Bst/Rpl24+ involves: C57BLKS	abnormal cell cycle	J:92052
	abnormal cell physiology	J:92052
	abnormal digit morphology	J:92052
	abnormal eye development	J:43133
	abnormal eye size	J:53381
	abnormal optic cup morphology	J:53381
	abnormal optic nerve morphology	J:43133
	abnormal retina ganglion layer morphology	J:43133, J:92052
	abnormal retina inner plexiform layer morphology	J:43133
	abnormal retina layer morphology	J:43133
	abnormal retina morphology	J:43133, J:60921
	abnormal retina neuronal layer morphology	J:43133
	abnormal retina progenitor cell morphology	J:53381
	absent optic nerve	J:43133
	belly spot	J:13703, J:78801
	cataract	J:60921
	caudal vertebral fusion	J:92052
	decreased body weight	J:92052
	decreased caudal vertebrae number	J:92052
	decreased embryo size	J:53381
	decreased retina ganglion cell number	J:43133
	delayed optic fissure closure	J:43133, J:53381
	disorganized retina inner nuclear layer	J:43133
	disorganized retina outer nuclear layer	J:43133
	embryonic lethality, incomplete penetrance	J:53381
	exencephaly	J:43133, J:53381
	impaired pupillary reflex	J:43133
	increased lumbar vertebrae number	J:92052
	kinked tail	J:13703, J:28035, J:53381, J:78801
	optic nerve atrophy	J:28035
	optic nerve coloboma	J:43133, J:60921
	optic nerve hypoplasia	J:43133
	pathological neovascularization	J:60921
	persistence of hyaloid vascular system	J:60921
	polydactyly	J:13703, J:43133, J:53381, J:78801
	prenatal lethality, complete penetrance	J:28035
	retina detachment	J:43133, J:60921
	retina fold	J:43133, J:60921
	retina hypoplasia	J:43133
	retina neovascularization	J:60921
	short tail	J:13703, J:78801
	thin retina ganglion layer	J:43133
	thin retina inner nuclear layer	J:43133
	white spotting	J:28035, J:43133
Rpl24Bst/Rpl24Bst involves: C57BLKS	embryonic lethality, complete penetrance	J:92052