98 phenotypes from 2 alleles in 6 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Chrdtm1Emdr/Chrdtm1Emdr 129S6.129-Chrdtm1Emdr	abnormal ear development	J:146769
	abnormal ear position	J:146769
	abnormal pharyngeal arch artery morphology	J:146769
	absent mandible	J:146769
	athymia	J:146769
	cleft palate	J:146769
	persistent truncus arteriosus	J:146769
	short mandible	J:146769
Chrdtm1Emdr/Chrdtm1Emdr either: B6SJL.129-Chrdtm1Emdr or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * SJL/J)	abnormal aortic arch morphology	J:83662
	abnormal artery morphology	J:83662
	abnormal brachiocephalic trunk morphology	J:83662
	abnormal common carotid artery morphology	J:83662
	abnormal cranial ganglia morphology	J:83662
	abnormal ear position	J:83662
	abnormal embryonic tissue morphology	J:83662
	abnormal extraembryonic tissue morphology	J:83662
	abnormal laryngeal cartilage morphology	J:83662
	abnormal mandible morphology	J:83662
	abnormal mesoderm development	J:83662
	abnormal middle ear morphology	J:83662
	abnormal neural crest cell migration	J:83662
	abnormal neural plate morphology	J:83662
	abnormal oropharynx morphology	J:83662
	abnormal pharyngeal pouch morphology	J:83662
	abnormal secondary palate development	J:83662
	abnormal thoracic vertebrae morphology	J:83662
	abnormal thyroid gland morphology	J:83662
	abnormal trigeminal ganglion morphology	J:83662
	abnormal tympanic ring morphology	J:83662
	abnormal vertebral arch development	J:83662
	abnormal vestibulocochlear ganglion morphology	J:83662
	absent arcus anterior	J:83662
	absent auditory tube	J:83662
	absent esophagus	J:83662
	absent inner ear	J:83662
	absent mandibular angle	J:83662
	absent mandibular condyloid process	J:83662
	absent mandibular coronoid process	J:83662
	absent mesoderm	J:83662
	absent nodose ganglion	J:83662
	absent notochord	J:83662
	absent parathyroid glands	J:83662
	absent petrosal ganglion	J:83662
	absent pharyngeal arches	J:83662
	absent pulmonary trunk	J:83662
	absent somites	J:83662
	absent temporal bone squamous part	J:83662
	athymia	J:83662
	cleft secondary palate	J:83662
	cricoid cartilage hypoplasia	J:83662
	cyanosis	J:83662
	decreased body size	J:83662
	decreased embryo size	J:83662
	decreased tympanic ring size	J:83662
	embryonic lethality between somite formation and embryo turning, complete penetrance	J:83662
	enlarged allantois	J:83662
	fusion of basioccipital and basisphenoid bone	J:83662
	heart right ventricle hypertrophy	J:83662
	hemorrhage	J:83662
	hydrops fetalis	J:83662
	hyoid bone hypoplasia	J:83662
	increased vasodilation	J:83662
	lethality throughout fetal growth and development, incomplete penetrance	J:83662
	microcephaly	J:83662
	palatal shelves fail to meet at midline	J:83662
	perinatal lethality, complete penetrance	J:83662
	persistent truncus arteriosus	J:83662
	presphenoid bone hypoplasia	J:83662
	retroesophageal right subclavian artery	J:83662
	right aortic arch	J:83662
	short zygomatic arch	J:83662
	small ears	J:83662
small geniculate ganglion	J:83662
small mandible	J:83662
small nodose ganglion	J:83662
small otic capsule	J:83662
small otic vesicle	J:83662
small petrosal ganglion	J:83662
small pharynx	J:83662
small temporal bone	J:83662
small trachea	J:83662
small vertebral body	J:83662
thyroid cartilage hypoplasia	J:83662
thyroid gland hypoplasia	J:83662
Chrdtm1Emdr/Chrdtm1Emdr involves: 129S1/Sv * 129X1/SvJ	abnormal brain development	J:123318
	abnormal miniature excitatory postsynaptic currents	J:123318
	abnormal response to novel object	J:123318
	abnormal spatial learning	J:123318
	decreased exploration in new environment	J:123318
	enhanced long-term potentiation	J:123318
	enhanced paired-pulse facilitation	J:123318
	hyperactivity	J:123318
	increased neurotransmitter release	J:123318
	normal nervous system phenotype	J:123318
	perinatal lethality, incomplete penetrance	J:123318
Chrdtm1Emdr/Chrdtm1Emdr involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * SJL/J	abnormal cardiovascular development	J:60303
	abnormal ear development	J:60303
	abnormal pharyngeal arch morphology	J:60303
	perinatal lethality, complete penetrance	J:60303
Chrdtm1Emdr/Chrdtm1Emdr involves: 129S1/Sv * 129X1/SvJ * ICR	normal mortality/aging	J:137629
	normal renal/urinary system phenotype	J:130204
	normal reproductive system phenotype	J:130204
Chrdtm2.1Vlcg/Chrdtm2.1Vlcg involves: 129S6/SvEvTac * C57BL/6NTac	no abnormal phenotype detected	J:200671