41 phenotypes from multigenic genotypes

Allelic Composition Genetic Background	Annotated Term	Reference
Arb2aTg(Tyr)TpNpin/Arb2a+ involves: FVB/N	head spot	J:260599
Arb2aTg(Tyr)TpNpin/Arb2aTg(Tyr)TpNpin involves: FVB/N	abnormal cranial nerve morphology	J:260599
	abnormal craniofacial morphology	J:260599
	abnormal facial nerve morphology	J:260599
	abnormal heart morphology	J:260599
	abnormal neural crest cell migration	J:260599
	abnormal oropharynx morphology	J:260599
	abnormal outer ear morphology	J:260599
	abnormal semicircular canal morphology	J:260599
	abnormal seminiferous tubule morphology	J:329885
	abnormal uterine horn morphology	J:260599
	absent coat pigmentation	J:260599
	blepharoptosis	J:260599
	circling	J:260599
	cleft palate	J:260599
	cryptorchism	J:260599
	decreased cell proliferation	J:260599
	decreased neural crest cell proliferation	J:260599
	delayed fontanelle closure	J:260599
	delayed vaginal opening	J:260599
	normal digestive/alimentary phenotype	J:260599
	exencephaly	J:260599
	facial asymmetry	J:260599
	heart left ventricle hypertrophy	J:260599
	hydrocephaly	J:260599
	impaired olfaction	J:260599
	increased heart weight	J:260599
	increased neural crest cell apoptosis	J:260599
	olfactory bulb hypoplasia	J:260599
	postnatal growth retardation	J:260599
	postnatal lethality, incomplete penetrance	J:260599
	reduced fertility	J:260599
	renal hypoplasia	J:260599
	retina coloboma	J:260599
	sex reversal	J:260599
	small penis	J:260599
	small seminal vesicle	J:260599
	thymus hypoplasia	J:260599
Arb2aTg(Tyr)TpNpin/Arb2aTg(Tyr)TpNpin Gata4tm1(cre)Svs/Gata4+ involves: 129S1/Sv * 129X1/SvJ * FVB/N	abnormal neural crest cell migration	J:260599
Chd7Gt(S20-7E1)Sor/Chd7+ Arb2aTg(Tyr)TpNpin/Arb2a+ involves: 129S4/SvJaeSor * C57BL/6 * FVB/N	abnormal optic fissure closure	J:260599
	circling	J:260599
	decreased body size	J:260599
	postnatal lethality, incomplete penetrance	J:260599
	prenatal lethality, incomplete penetrance	J:260599
	retina coloboma	J:260599
	sex reversal	J:260599