92 phenotypes from 6 alleles in 8 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Aldh1a2grim/Aldh1a2grim involves: 129S1/Sv * C57BL/6	abnormal embryo turning	J:185330
	abnormal first pharyngeal arch morphology	J:185330
	abnormal heart tube morphology	J:185330
	abnormal otic vesicle morphology	J:185330
	abnormal pharyngeal arch morphology	J:185330
	abnormal vitamin A metabolism	J:185330
	absent forelimb buds	J:185330
	absent pharyngeal arches	J:185330
	decreased somite size	J:185330
	embryonic growth arrest	J:185330
	embryonic lethality during organogenesis, complete penetrance	J:185330
	failure of heart looping	J:185330
	small first pharyngeal arch	J:185330
	small forelimb buds	J:185330
	small otic vesicle	J:185330
Aldh1a2grim/Aldh1a2grim involves: 129S1/Sv * C57BL/6 * FVB/NJ	abnormal glossopharyngeal ganglion morphology	J:171522
	abnormal mandibular prominence morphology	J:171522
	abnormal maxillary prominence morphology	J:171522
	abnormal nervous system development	J:171522
	abnormal trigeminal ganglion morphology	J:171522
	abnormal vagus ganglion morphology	J:171522
	abnormal vascular development	J:171522
	abnormal vestibulocochlear ganglion morphology	J:171522
	absent fourth pharyngeal arch	J:171522
	absent pharyngeal arch arteries	J:171522
	absent third pharyngeal arch	J:171522
	decreased embryo size	J:171522
	embryonic lethality during organogenesis, complete penetrance	J:171522
Aldh1a2tm1Dll/Aldh1a2tm1Dll Not Specified	aberrant origin of the right subclavian artery	J:81969
	abnormal aortic arch and aortic arch branch attachment	J:81969
	abnormal artery morphology	J:81969
	abnormal common carotid artery morphology	J:81969
	abnormal left subclavian artery morphology	J:81969
	abnormal truncus arteriosus septation	J:81969
	cervical aortic arch	J:81969
	cyanosis	J:81969
	decreased body size	J:81969
	decreased tracheal cartilage ring number	J:81969
	postnatal lethality, incomplete penetrance	J:81969
	short trachea	J:81969
Aldh1a2tm1Dll/Aldh1a2tm1Ipc involves: CD-1	aberrant origin of the right subclavian artery	J:81969
	abnormal artery morphology	J:81969
	abnormal common carotid artery morphology	J:81969
	abnormal cranial nerve morphology	J:81969
	abnormal cricoid cartilage morphology	J:81969
	abnormal laryngeal cartilage morphology	J:81969
	abnormal left subclavian artery morphology	J:81969
	abnormal neural crest cell migration	J:81969
	abnormal pharyngeal arch artery morphology	J:81969
	abnormal pharyngeal pouch morphology	J:81969
	abnormal third pharyngeal arch artery morphology	J:81969
	abnormal thyroid cartilage morphology	J:81969
	abnormal tracheal cartilage morphology	J:81969
	absent parathyroid glands	J:81969
	absent third pharyngeal arch	J:81969
	athymia	J:81969
	conotruncal ridge hypoplasia	J:81969
	cyanosis	J:81969
	decreased body size	J:81969
	double aortic arch	J:81969
	fusion of glossopharyngeal and vagus nerve	J:81969
	persistent truncus arteriosus	J:81969
	pharyngeal arch hypoplasia	J:81969
	postnatal lethality, complete penetrance	J:81969
	right aortic arch	J:81969
	short trachea	J:81969
	thymus hypoplasia	J:81969
	ventricular septal defect	J:81969
Aldh1a2tm1Dll/Aldh1a2tm1Ipc Tg(Rarb-cre)1Mrc/0 Not Specified	abnormal digit morphology	J:97213
	abnormal motor neuron innervation pattern	J:97213
	normal muscle phenotype	J:97213
	normal skeleton phenotype	J:97213
	syndactyly	J:97213
Aldh1a2tm1Gdu/Aldh1a2tm1Gdu involves: 129S1/Sv * 129X1/SvJ * C57BL/6	abnormal heart development	J:75950
	absent second pharyngeal arch	J:75950
	absent third pharyngeal arch	J:75950
	decreased body length	J:75950
	decreased embryo size	J:75950
	decreased somite size	J:75950
	embryonic lethality during organogenesis, complete penetrance	J:75950
	failure of heart looping	J:75950
	small otic vesicle	J:75950
Aldh1a2tm1Gdu/Aldh1a2tm1Gdu involves: 129S1/Sv * 129X1/SvJ * Swiss Webster	renal hypoplasia	J:157254
Aldh1a2tm1Gdu/Aldh1a2tm1Gdu Tg(Hoxb7-EGFP)33Cos/0 involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA * Swiss Webster	impaired branching involved in ureteric bud morphogenesis	J:157254
Aldh1a2tm1Ipc/Aldh1a2tm1Ipc Not Specified	abnormal embryo turning	J:54067
	abnormal embryonic tissue morphology	J:54067
	abnormal fetal atrioventricular canal morphology	J:67816
	abnormal fetal cardiomyocyte morphology	J:67816
	abnormal heart development	J:54067, J:67816
	abnormal myocardium layer morphology	J:67816
	abnormal neural tube morphology	J:54067
	abnormal pharyngeal arch morphology	J:54067
	abnormal somite development	J:54067
	abnormal vitelline vasculature morphology	J:54067
	absent atrioventricular cushions	J:67816
	absent hindlimb buds	J:54067
	absent myocardial trabeculae	J:54067
	absent Wolffian ducts	J:54067
	caudal body truncation	J:54067
	decreased embryo size	J:54067
	decreased somite size	J:54067
	embryonic lethality during organogenesis, complete penetrance	J:54067
	enlarged heart	J:54067
	failure of heart looping	J:54067, J:67816
	failure of ventral body wall closure	J:54067
	incomplete caudal neuropore closure	J:54067
	otic vesicle hypoplasia	J:54067
	small frontonasal prominence	J:54067
	thick myocardium	J:67816
Aldh1a2tm1Soc/Aldh1a2tm1Soc Not Specified	embryonic lethality, complete penetrance	J:112635
Aldh1a2tm1Soc/Aldh1a2tm2Soc Not Specified	no abnormal phenotype detected	J:112635
Aldh1a2tm1Soc/Aldh1a2tm2Soc Isl1tm1(cre)Tmj/Isl1+ involves: 129X1/SvJ	abnormal motor neuron innervation pattern	J:112635
	decreased motor neuron number	J:112635
Aldh1a2tm1Soc/Aldh1a2tm2Soc Tg(Dll1-cre)1Gos/0 Not Specified	abnormal motor neuron innervation pattern	J:112635
	abnormal vitamin A level	J:112635
	decreased motor neuron number	J:112635
	normal limbs/digits/tail phenotype	J:112635