23 phenotypes from 1 allele in 4 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Anp32btm1Mak/Anp32btm1Mak B6.129P2-Anp32btm1Mak	abnormal craniofacial morphology	J:172042
	abnormal inner ear morphology	J:172042
	cleft palate	J:172042
	enlarged brain ventricles	J:172042
	perinatal lethality, incomplete penetrance	J:172042
	primary atelectasis	J:172042
Anp32btm1Mak/Anp32btm1Mak C.129P2(B6)-Anp32btm1Mak	decreased body weight	J:227403
	decreased circulating bilirubin level	J:227403
	decreased circulating cholesterol level	J:227403
	decreased circulating HDL cholesterol level	J:227403
	decreased circulating total protein level	J:227403
	increased incidence of tumors by chemical induction	J:227403
	postnatal lethality, incomplete penetrance	J:227403
	premature death	J:227403
	normal reproductive system phenotype	J:227403
Anp32btm1Mak/Anp32btm1Mak FVB.129P2(B6)-Anp32btm1Mak	postnatal lethality, incomplete penetrance	J:227403
Anp32btm1Mak/Anp32btm1Mak involves: 129P2/OlaHsd * C57BL/6	abnormal craniofacial morphology	J:172042
	abnormal inner ear morphology	J:172042
	normal cellular phenotype	J:172042
	cleft palate	J:172042
	decreased body size	J:172042
	decreased body weight	J:172042
	enlarged brain ventricles	J:172042
	hematoma	J:172042
	hydroureter	J:172042
	kyphosis	J:172042
	megacolon	J:172042
	perinatal lethality, incomplete penetrance	J:172042
	polyploidy	J:172042
	premature aging	J:172042
	premature death	J:172042
	primary atelectasis	J:172042