62 phenotypes from 6 alleles in 6 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Afdnem1(IMPC)Mbp/Afdn+ C57BL/6N-Afdnem1(IMPC)Mbp/MbpMmucd	abnormal cecum morphology	J:211773
	abnormal gallbladder morphology	J:211773
	abnormal heart morphology	J:211773
	abnormal hindbrain development	J:211773
	abnormal kidney morphology	J:211773
	abnormal liver morphology	J:211773
	abnormal lymph node morphology	J:211773
	abnormal neural tube closure	J:211773
	abnormal neural tube morphology	J:211773
	abnormal skin morphology	J:211773
	abnormal spleen morphology	J:211773
	abnormal urinary bladder morphology	J:211773
	abnormal uterus morphology	J:211773
	cystolithiasis	J:211773
	decreased lymphocyte cell number	J:211773
	decreased prepulse inhibition	J:211773
	decreased spleen weight	J:211773
	enlarged kidney	J:211773
	enlarged liver	J:211773
	enlarged lymph nodes	J:211773
	enlarged spleen	J:211773
	increased hematocrit	J:211773
	small heart	J:211773
	small spleen	J:211773
Afdnem1(IMPC)Mbp/Afdnem1(IMPC)Mbp C57BL/6N-Afdnem1(IMPC)Mbp/MbpMmucd	embryonic lethality prior to organogenesis	J:211773
	preweaning lethality, complete penetrance	J:211773
Afdntm1.1Lfr/Afdntm1.1Lfr Neurod6tm1(cre)Kan/Neurod6+ involves: 129 * C57BL/6 * SJL	abnormal excitatory postsynaptic potential	J:179366
	abnormal hippocampus CA1 region morphology	J:179366
	abnormal hippocampus pyramidal cell morphology	J:179366
	abnormal synapse morphology	J:179366
	ectopic hippocampus pyramidal cells	J:179366
Afdntm1c(EUCOMM)Hmgu/Afdntm1c(EUCOMM)Hmgu Emx1tm1(cre)Krj/Emx1+ involves: 129S2/SvPas * C57BL/6J * C57BL/6N	abnormal cell cycle	J:215584
	abnormal cerebral cortex morphology	J:215584
	abnormal cortical ventricular zone morphology	J:215584
	abnormal embryonic neuroepithelium morphology	J:215584
	abnormal hippocampus morphology	J:215584
	abnormal neocortex morphology	J:215584
	abnormal nervous system tract morphology	J:215584
	abnormal radial glial cell morphology	J:215584
	abnormal stratification in cerebral cortex	J:215584
	abnormal telencephalon development	J:215584
	ectopic neuron	J:215584
	increased brain size	J:215584
	increased neocortex size	J:215584
	increased neuronal precursor cell number	J:215584
	increased radial glial cell number	J:215584
	thin cortical plate	J:215584
Afdntm1Mrcr/Afdntm1Mrcr involves: 129S1/Sv * 129X1/SvJ	abnormal ectoderm development	J:57046
	abnormal embryonic neuroepithelium morphology	J:57046
	abnormal germ layer development	J:57046
	abnormal mesoderm development	J:57046
	abnormal rostral-caudal body axis extension	J:57046
	absent allantois	J:57046
	absent neural folds	J:57046
	absent notochord	J:57046
	absent somites	J:57046
	decreased embryo size	J:57046
	embryonic growth arrest	J:57046
	embryonic lethality during organogenesis, complete penetrance	J:57046
Afdntm1Ytk/Afdntm1Ytk involves: 129X1/SvJ * C57BL/6 * DBA/2	abnormal amniotic cavity morphology	J:57589
	abnormal ectoderm development	J:57589
	abnormal extraembryonic coelom morphology	J:57589
	abnormal mesoderm development	J:57589
	abnormal neural tube morphology	J:57589
	abnormal somite development	J:57589
	absent allantois	J:57589
	absent heart	J:57589
	decreased embryo size	J:57589
	embryonic lethality during organogenesis, complete penetrance	J:57589
Afdntm2Ytk/Afdntm2Ytk Tg(Camk2a-cre)1Gsc/0 involves: FVB/N	abnormal synapse morphology	J:151436