56 phenotypes from 4 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Pcntem1(IMPC)Mbp/Pcnt+ C57BL/6NCrl-Pcntem1(IMPC)Mbp/MbpMmucd	abnormal eye morphology	J:211773
	abnormal kidney morphology	J:211773
	abnormal skin morphology	J:211773
	abnormal testis morphology	J:211773
	anophthalmia	J:211773
	decreased body length	J:211773
	persistence of hyaloid vascular system	J:211773
	small kidney	J:211773
	small testis	J:211773
Pcntem1(IMPC)Mbp/Pcntem1(IMPC)Mbp C57BL/6NCrl-Pcntem1(IMPC)Mbp/MbpMmucd	embryonic growth retardation	J:211773
	microphthalmia	J:211773
	preweaning lethality, complete penetrance	J:211773
PcntGt(RRU388)Byg/PcntGt(RRU388)Byg B6.129P2-PcntGt(RRU388)Byg	abnormal brain development	J:226309
	abnormal cortical ventricular zone morphology	J:226309
	abnormal craniofacial development	J:226309
	abnormal embryonic neuroepithelium morphology	J:226309
	abnormal eye morphology	J:226309
	abnormal head shape	J:226309
	abnormal heart morphology	J:226309
	abnormal heart septum morphology	J:226309
	abnormal hippocampus morphology	J:226309
	abnormal kidney morphology	J:226309
	abnormal mitotic spindle morphology	J:226309
	abnormal neuron differentiation	J:226309
	abnormal vascular development	J:226309
	anophthalmia	J:226309
	aortic valve regurgitation	J:226309
	atelectasis	J:226309
	atrial septal defect	J:226309
	atrioventricular septal defect	J:226309
	cleft palate	J:226309
	congestive heart failure	J:226309
	decreased brain size	J:226309
	decreased surfactant secretion	J:226309
	duplex kidney	J:226309
	enlarged brain ventricles	J:226309
	hemorrhage	J:226309
	hydrops fetalis	J:226309
	increased heart ventricle size	J:226309
	intracranial hemorrhage	J:226309
	kidney cortex cyst	J:226309
	kidney cyst	J:226309
	lethality throughout fetal growth and development, complete penetrance	J:226309
	microcephaly	J:226309
	microphthalmia	J:226309
	misaligned sternebrae	J:226309
	mitral valve regurgitation	J:226309
	overriding aortic valve	J:226309
	polydactyly	J:226309
	prenatal growth retardation	J:226309
	pulmonary hypoplasia	J:226309
	renal glomerulus cyst	J:226309
	syndactyly	J:226309
	thin cerebral cortex	J:226309
	thin cortical plate	J:226309
	ventricular septal defect	J:226309
Pcntm239Asp/Pcnt+ Tg(Rr291-lacZ)#Mekk/0 involves: C57BL/6J * FVB/N	premature death	J:136795
	sporadic seizures	J:136795
Pcntm239Asp/Pcntm239Asp Tg(Rr291-lacZ)#Mekk/0 involves: C57BL/6J * FVB/N	abnormal cerebral cortex morphology	J:136795
	polydactyly	J:136795
Pcntm275Asp/Pcnt+ Tg(Rr291-lacZ)#Mekk/0 involves: C57BL/6J * FVB/N	premature death	J:136795
	sporadic seizures	J:136795
Pcntm275Asp/Pcntm275Asp Tg(Rr291-lacZ)#Mekk/0 involves: C57BL/6J * FVB/N	abnormal cerebral cortex morphology	J:136795
	perinatal lethality	J:136795
	polydactyly	J:136795