124 phenotypes from 10 alleles in 11 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Ednram1Mhda/Ednra+ C3HeB/FeJ-Ednram1Mhda	abnormal cranium morphology	J:237903
	abnormal incudomalleolar joint morphology	J:237903
	abnormal inspiratory capacity	J:237903
	abnormal malleus morphology	J:237903
	abnormal respiration	J:237903
	abnormal temporal bone petrous part morphology	J:237903
	abnormal temporal bone zygomatic process morphology	J:237903
	abnormal vital capacity	J:237903
	abnormal zygomatic bone morphology	J:237903
	absent incus short process	J:237903
	absent temporal bone zygomatic process	J:237903
	decreased prepulse inhibition	J:237903
	decreased startle reflex	J:237903
	impaired hearing	J:237903
	increased or absent threshold for auditory brainstem response	J:237903
	normal integument phenotype	J:237903
	malocclusion	J:237903
	micrognathia	J:237903
	short mandible	J:237903
Ednram1Mhda/Ednram1Mhda C3HeB/FeJ-Ednram1Mhda	abnormal cranium morphology	J:237903
	abnormal ear shape	J:237903
	abnormal inspiratory capacity	J:237903
	abnormal jaw morphology	J:237903
	abnormal malleus morphology	J:237903
	abnormal mandibular condyloid process morphology	J:237903
	abnormal orbit morphology	J:237903
	abnormal outer ear helix morphology	J:237903
	abnormal respiration	J:237903
	abnormal temporal bone petrous part morphology	J:237903
	abnormal temporomandibular joint morphology	J:237903
	abnormal vital capacity	J:237903
	abnormal zygomatic arch morphology	J:237903
	abnormal zygomatic bone morphology	J:237903
	absent incus short process	J:237903
	absent temporal bone zygomatic process	J:237903
	conductive hearing loss	J:237903
	decreased body size	J:237903
	decreased body weight	J:237903
	decreased lung compliance	J:237903
	decreased prepulse inhibition	J:237903
	decreased startle reflex	J:237903
	decreased total lung capacity	J:237903
	increased or absent threshold for auditory brainstem response	J:237903
	normal integument phenotype	J:237903
	lowered ear position	J:237903
	macrophthalmia	J:237903
	malocclusion	J:237903
	micrognathia	J:237903
	prominent cheeks	J:237903
	round face	J:237903
	round orbits	J:237903
	short mandible	J:237903
	short snout	J:237903
	shortened head	J:237903
	wide coronal suture	J:237903
	wide lambdoid suture	J:237903
	wide sagittal suture	J:237903
Ednratm1b(EUCOMM)Hmgu/Ednratm1b(EUCOMM)Hmgu C57BL/6N-Ednratm1b(EUCOMM)Hmgu/J	abnormal craniofacial morphology	J:211773
	abnormal facial morphology	J:211773
	preweaning lethality, complete penetrance	J:211773
Ednratm1Hku/Ednratm1Hku involves: 129 * C57BL/6 * ICR	abnormal alisphenoid bone morphology	J:131382
	abnormal alveolar process morphology	J:131382
	abnormal basisphenoid bone morphology	J:131382
	abnormal hyoid bone morphology	J:131382
	abnormal malleus morphology	J:131382
	abnormal palatine bone morphology	J:131382
	abnormal pterygoid process morphology	J:131382
	abnormal stapes morphology	J:131382
	abnormal temporal bone zygomatic process morphology	J:131382
	abnormal zygomatic bone morphology	J:131382
	absent gonial bone	J:131382
	absent temporal bone zygomatic process	J:131382
	absent tympanic ring	J:131382
	lower jaw to upper jaw transformation	J:131382
	perinatal lethality, complete penetrance	J:131382
	short styloid process	J:131382
Ednratm1Hku/Ednratm2.1Hku involves: 129 * C57BL/6 * ICR	perinatal lethality, complete penetrance	J:131382
Ednratm1Hku/Ednratm3(Ednrb)Hku involves: 129 * C57BL/6 * ICR	perinatal lethality, complete penetrance	J:131382
Ednratm1Ywa/Ednratm1Ywa 129S/SvEv-Ednratm1Ywa	abnormal cardiovascular system morphology	J:46639
	abnormal carotid artery morphology	J:46639
	abnormal dorsal aorta morphology	J:46639
	abnormal facial nerve morphology	J:46639
	abnormal first pharyngeal arch morphology	J:46639
	abnormal mandibular nerve branching	J:46639
	abnormal middle ear ossicle morphology	J:46639
	abnormal mouth morphology	J:46639
	abnormal muscle morphology	J:46639
	abnormal outer ear morphology	J:46639
	abnormal palate morphology	J:46639
	abnormal palatine bone morphology	J:46639
	abnormal pulmonary ventilation	J:46639
	abnormal skeleton morphology	J:46639
	abnormal styloid process morphology	J:46639
	abnormal trigeminal nerve morphology	J:46639
	absent incus	J:46639
	absent malleus	J:46639
	absent Meckel's cartilage	J:46639
	absent right subclavian artery	J:46639
	absent salivary gland	J:46639
	absent stapes	J:46639
	absent submandibular gland	J:46639
	absent tubotympanic recess	J:46639
	absent tympanic membrane	J:46639
	absent tympanic ring	J:46639
	aorta tubular hypoplasia	J:46639
	cleft chin	J:46639
	d-loop transposition of the great arteries	J:46639
	double outlet right ventricle	J:46639
	ectopic thymus	J:46639
	interrupted aorta	J:46639
	mandible hypoplasia	J:46639
	overriding aortic valve	J:46639
	patent ductus arteriosus	J:46639
	perimembraneous ventricular septal defect	J:46639
	perinatal lethality, complete penetrance	J:46639
	persistent truncus arteriosus	J:46639
	small second pharyngeal arch	J:46639
	small zygomatic bone	J:46639
	thymus hypoplasia	J:46639
	tongue hypoplasia	J:46639
Ednratm1Ywa/Ednratm1Ywa involves: 129S7/SvEvBrd	abnormal alisphenoid bone morphology	J:93183
	abnormal mandible morphology	J:93183
	abnormal maxilla morphology	J:93183
	abnormal Meckel's cartilage morphology	J:93183
	abnormal mouth floor morphology	J:93183
	abnormal palatine bone morphology	J:93183
	absent gonial bone	J:93183
	absent tympanic ring	J:93183
	lower jaw to upper jaw transformation	J:93183
	small zygomatic bone	J:93183
Ednratm1Ywa/Ednratm1Ywa involves: 129S7/SvEvBrd * C57BL/6 * CBA	aberrant origin of the right subclavian artery	J:48566
	abnormal artery morphology	J:48566
	abnormal ascending aorta morphology	J:48566
	abnormal fourth pharyngeal arch artery morphology	J:48566
	abnormal pharyngeal arch artery morphology	J:48566
	abnormal sixth pharyngeal arch artery morphology	J:48566
	abnormal third pharyngeal arch artery morphology	J:48566
	double aortic arch	J:48566
	double outlet right ventricle	J:48566
	overriding aortic valve	J:48566
	persistent right 6th pharyngeal arch artery	J:48566
	persistent right dorsal aorta	J:48566
	persistent truncus arteriosus	J:48566
Ednratm2.1Hku/Ednratm2.1Hku involves: 129 * C57BL/6 * ICR	abnormal temporal bone morphology	J:224515
	absent Meckel's cartilage	J:224515
	perinatal lethality, complete penetrance	J:131382
Ednratm2.1Hku/Ednratm3(Ednrb)Hku involves: 129 * C57BL/6 * ICR	abnormal craniofacial bone morphology	J:131382
	abnormal hyoid bone morphology	J:131382
	abnormal mandible morphology	J:131382
	lower jaw to upper jaw transformation	J:131382
	perinatal lethality, complete penetrance	J:131382
Ednratm2.1Hku/Ednratm4(Ednra)Hku involves: 129 * C57BL/6 * ICR	normal craniofacial phenotype	J:131382
Ednratm2.1Hku/Ednratm5Hku involves: 129 * C57BL/6 * ICR	abnormal heart development	J:166932
	abnormal heart morphology	J:166932
	abnormal heart ventricle morphology	J:166932
Ednratm2Hku/Ednratm2Hku involves: 129 * C57BL/6 * ICR	perinatal lethality, complete penetrance	J:131382
Ednratm2Hku/Ednratm3(Ednrb)Hku involves: 129 * C57BL/6 * ICR	abnormal craniofacial bone morphology	J:131382
	abnormal hyoid bone morphology	J:131382
	abnormal mandible morphology	J:131382
	perinatal lethality, complete penetrance	J:131382
Ednratm2Ywa/Ednratm2Ywa involves: 129S6/SvEvTac * C57BL/6J * FVB/N	no abnormal phenotype detected	J:86476
Ednratm2Ywa/Ednratm2Ywa H2az2Tg(Wnt1-cre)11Rth/H2az2+ involves: C57BL/6J * CBA/J	abnormal craniofacial bone morphology	J:149166
	abnormal craniofacial morphology	J:149166
	abnormal incisor morphology	J:149166
	abnormal incus morphology	J:149166
	abnormal malleus morphology	J:149166
	abnormal mandible morphology	J:149166
	abnormal mouth floor morphology	J:149166
	abnormal stapes morphology	J:149166
	absent incus	J:149166
	absent malleus	J:149166
	absent Meckel's cartilage	J:149166
	facial cleft	J:149166
	short mandible	J:149166
	tongue hypoplasia	J:149166
Ednratm2Ywa/Ednratm2Ywa Tg(Aqp2-cre)1Dek/0 involves: 129S7/SvEvBrd * C57BL/6 * SJL	abnormal urine osmolality	J:101241
	normal homeostasis/metabolism phenotype	J:101241
	increased circulating antidiuretic hormone level	J:101241
	normal renal/urinary system phenotype	J:101241
Ednratm2Ywa/Ednratm2Ywa Tg(AQP2-cre)2Dek/0 involves: 129S6/SvEvTac * C57BL/6 * CBA	normal cardiovascular system phenotype	J:116002
	no abnormal phenotype detected	J:116002
Ednratm2Ywa/Ednratm2Ywa Tg(Hand2-cre)7-1Clou/0 involves: C57BL/6J * SJL	normal craniofacial phenotype	J:149166
Ednratm2Ywa/Ednratm2Ywa Tg(Myh6-cre)2182Mds/0 involves: 129S6/SvEvTac * C57BL/6J * FVB/N	no abnormal phenotype detected	J:86476
Ednratm3(Ednrb)Hku/Ednratm3(Ednrb)Hku involves: 129 * C57BL/6 * ICR	abnormal craniofacial bone morphology	J:131382
	abnormal hyoid bone morphology	J:131382
	abnormal mandible morphology	J:131382
	perinatal lethality, complete penetrance	J:131382