26 phenotypes from 4 alleles in 5 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Ptf1atm1.1(cre)Cvw/Ptf1atm1.1(cre)Cvw involves: 129S1/Sv * 129X1/SvJ	abnormal eye development	J:115271
	abnormal retina morphology	J:115271
	abnormal retina outer plexiform layer morphology	J:200752
	absent amacrine cells	J:115271
	absent pancreas	J:130251
	absent retina horizontal cells	J:115271
	absent retina inner plexiform layer	J:115271
	increased retina ganglion cell number	J:115271
	neonatal lethality, complete penetrance	J:130251
	thick retina ganglion layer	J:115271
Ptf1atm1Pkwe/Ptf1atm1Pkwe involves: 129P2/OlaHsd	abnormal cerebellum development	J:120017
	absent cerebellum	J:120017
	absent pancreas	J:120017
Ptf1atm1Pkwe/Ptf1atm1Pkwe involves: 129P2/OlaHsd * C57BL/6	abnormal spleen morphology	J:51571
	absent pancreas	J:51571
	cyanosis	J:51571
	decreased body weight	J:51571
	decreased pancreatic alpha cell number	J:51571
	hypoglycemia	J:51571
	neonatal lethality, complete penetrance	J:51571
Ptf1atm2.1Mgn/Ptf1atm2.1Mgn Not Specified	increased retina ganglion cell number	J:115271
Ptf1atm2Macd/Ptf1atm2Macd involves: 129S6/SvEvTac	abnormal cerebellar granule layer morphology	J:130251
	abnormal glutaminergic neuron morphology	J:130251
	abnormal neural tube morphology	J:130251
	abnormal neuron differentiation	J:130251
	abnormal pancreas development	J:125691
	abnormal spinal cord dorsal horn morphology	J:130251
	absent pancreas	J:130251
	decreased neuronal precursor cell number	J:130251
	loss of GABAergic neurons	J:130251
	neonatal lethality, complete penetrance	J:130251
	small cerebellum	J:130251