56 phenotypes from 4 alleles in 4 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Cc2d2ab2b1035Clo/Cc2d2ab2b1035Clo C57BL/6J-Cc2d2ab2b1035Clo	anophthalmia	J:175213
	atrioventricular septal defect	J:175213
	biventricular, discordant atrioventricular connection	J:175213
	cleft palate	J:175213
	common atrium	J:175213
	complete atrioventricular septal defect	J:175213
	double outlet right ventricle	J:175213
	double outlet right ventricle with atrioventricular septal defect	J:175213
	duplex kidney	J:175213
	heterotaxia	J:175213
	kidney cyst	J:175213
	microphthalmia	J:175213
	muscular ventricular septal defect	J:175213
	persistent truncus arteriosus	J:175213
	polycystic kidney	J:175213
	preaxial polydactyly	J:175213
	prenatal growth retardation	J:175213
	pulmonary valve atresia	J:175213
	superior-inferior ventricles	J:175213
	tricuspid valve atresia	J:175213
	ventricular septal defect	J:175213
Cc2d2aGt(AA0274)Wtsi/Cc2d2aGt(AA0274)Wtsi involves: 129P2/OlaHsd	abnormal left-right axis patterning	J:176174
	abnormal rostral-caudal axis patterning	J:176174
	normal cellular phenotype	J:176174
	holoprosencephaly	J:176174
	microphthalmia	J:176174
Cc2d2atm1a(EUCOMM)Wtsi/Cc2d2a+ C57BL/6N-Cc2d2atm1a(EUCOMM)Wtsi/Wtsi	decreased body weight	J:175295
Cc2d2atm1Asw/Cc2d2atm1Asw Not Specified	abnormal cochlear hair cell stereociliary bundle morphology	J:226310
	abnormal embryo development	J:226310
	abnormal eye electrophysiology	J:226310
	abnormal kinocilium morphology	J:226310
	abnormal neural tube morphology	J:226310
	abnormal nonmotile primary cilium morphology	J:226310
	abnormal photoreceptor inner segment morphology	J:226310
	abnormal photoreceptor outer segment morphology	J:226310
	abnormal primary cilium morphology	J:226310
	abnormal primitive node morphology	J:226310
	abnormal renal tubule epithelial cell primary cilium morphology	J:226310
	abnormal retina morphology	J:226310
	abnormal retina outer nuclear layer morphology	J:226310
	abnormal tracheal ciliated epithelium morphology	J:226310
	abnormal vesicle-mediated transport	J:226310
	anophthalmia	J:226310
	decreased embryo size	J:226310
	decreased embryonic cilium number	J:226310
	decreased embryonic neuroepithelium primary cilium number	J:226310
	decreased respiratory motile cilia number	J:226310
	dextrocardia	J:226310
	exencephaly	J:226310
	focal dorsal hair loss	J:226310
	hemorrhage	J:226310
	hydrocephaly	J:226310
	incomplete rostral neuropore closure	J:226310
	lethality throughout fetal growth and development, incomplete penetrance	J:226310
	lethargy	J:226310
	microphthalmia	J:226310
	polydactyly	J:226310
	postnatal growth retardation	J:226310
	preaxial polydactyly	J:226310
	situs inversus	J:226310