33 phenotypes from 1 allele in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Rpl27aSfa/Rpl27a+ C57BL/6J-Rpl27aSfa	abnormal bone marrow cell physiology	J:174216
	abnormal cerebellar granule layer morphology	J:174216
	abnormal cerebellar layer morphology	J:174216
	abnormal cerebellum external granule cell layer morphology	J:174216
	abnormal hematopoietic system morphology/development	J:174216
	abnormal Purkinje cell morphology	J:174216
	anemia	J:174216
	ataxia	J:174216
	decreased body weight	J:174216
	decreased bone marrow cell number	J:174216
	decreased cerebellar granule cell number	J:174216
	decreased erythrocyte cell number	J:174216
	decreased hematopoietic cell number	J:174216
	decreased hematopoietic stem cell number	J:174216
	decreased leukocyte cell number	J:174216
	ectopic Purkinje cell	J:174216
	hyperpigmentation	J:174216
	impaired coordination	J:174216
	increased ear pigmentation	J:174216
	increased foot pad pigmentation	J:174216
	increased hematopoietic stem cell proliferation	J:174216
	increased mortality induced by gamma-irradiation	J:174216
	increased tail pigmentation	J:174216
	pancytopenia	J:174216
	postnatal growth retardation	J:174216
	postnatal lethality, incomplete penetrance	J:174216
	small cerebellum	J:174216
	small spleen	J:174216
	small thymus	J:174216
	thin external granule cell layer	J:174216
	thrombocytopenia	J:174216
Rpl27aSfa/Rpl27a+ Tg(Dct-lacZ)#Ove/0 involves: C57BL/6J * FVB/N	abnormal epidermal melanocyte morphology	J:174216
	hyperpigmentation	J:174216
	increased foot pad pigmentation	J:174216
	increased tail pigmentation	J:174216
Rpl27aSfa/Rpl27aSfa C57BL/6J-Rpl27aSfa	embryonic lethality, complete penetrance	J:174216