23 phenotypes from 3 alleles in 5 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Esrrgtm1Dgen/Esrrg+ involves: 129P2/OlaHsd * C57BL/6	hyperekplexia	J:101679
Esrrgtm1Dgen/Esrrgtm1Dgen involves: 129P2/OlaHsd * C57BL/6	postnatal lethality, complete penetrance	J:101679, J:156955
Esrrgtm1Rev/Esrrg+ either: (involves: 129) or (involves: C57BL/6) or (involves: ICR)	bundle branch block	J:129851
	increased mitochondrial number	J:129851
	prolonged QRS complex duration	J:129851
Esrrgtm1Rev/Esrrgtm1Rev either: (involves: 129) or (involves: C57BL/6) or (involves: ICR)	abnormal impulse conducting system conduction	J:129851
	abnormal myocardial fiber physiology	J:129851
	abnormal respiratory electron transport chain	J:129851
	absent gastric milk in neonates	J:129851
	bundle branch block	J:129851
	decreased birth weight	J:129851
	increased circulating lactate level	J:129851
	increased mitochondrial number	J:129851
	postnatal lethality, complete penetrance	J:129851
	prolonged QRS complex duration	J:129851
	prolonged QT interval	J:129851
	prolonged ST segment	J:129851
Esrrgtm1Rev/Esrrgtm1Rev involves: C57BL/6	postnatal lethality, complete penetrance	J:156955
Esrrgtm1Rev/Esrrgtm1Rev Not Specified	abnormal kidney medulla morphology	J:168796
	abnormal kidney papilla morphology	J:168796
	abnormal kidney pelvis morphology	J:168796
	abnormal renal glomerulus morphology	J:168796
	absent kidney papilla	J:168796
Esrrgtm1Sjda/Esrrgtm1Sjda involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	abnormal auditory brainstem response waveform shape	J:211740
	decreased survivor rate	J:211740
	impaired hearing	J:211740
	increased or absent threshold for auditory brainstem response	J:211740
	postnatal lethality, incomplete penetrance	J:211740