17 phenotypes from multigenic genotypes

Allelic Composition Genetic Background	Annotated Term	Reference
Bace1tm1Pcw/Bace1+ Tg(Camk2a-tTA)1Mmay/0 Tg(tetO-CDK5R1/GFP)337Lht/0 involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	astrocytosis	J:177847
	normal behavior/neurological phenotype	J:177847
	decreased brain weight	J:177847
	hippocampal neuron degeneration	J:177847
	normal nervous system phenotype	J:177847
Bace1tm1Pcw/Bace1+ Tg(APP695)3Dbo/0 Tg(PSEN1dE9)S9Dbo/0 involves: 129S1/Sv * 129X1/SvJ * C3H/HeJ * C57BL/6J	abnormal spatial learning	J:123534
	abnormal spatial reference memory	J:123534
	amyloid beta deposits	J:123534
	amyloidosis	J:123534
Bace1tm1Pcw/Bace1tm1Pcw Tg(APP695)3Dbo/0 Tg(PSEN1dE9)S9Dbo/0 involves: 129S1/Sv * 129X1/SvJ * C3H/HeJ * C57BL/6J	abnormal locomotor activation	J:123534
	normal behavior/neurological phenotype	J:123534
	decreased anxiety-related response	J:123534
	normal nervous system phenotype	J:123534
Bace1tm1Psa/Bace1tm1Psa Bace2tm1Bdes/Bace2tm1Bdes either: (involves: 129/Sv * 129P2/OlaHsd * C57BL/6J) or (involves: 129/Sv * 129P2/OlaHsd * C57BL/6J * CD-1)	abnormal nervous system physiology	J:100925
	cachexia	J:100925
	decreased body size	J:100925
	postnatal lethality, incomplete penetrance	J:100925
Bace1tm1Psa/Bace1tm1Psa Nrg1tm4.1Cbm/Nrg1+ involves: 129P2/OlaHsd * 129S2/SvPas * BALB/cJ * C57BL/6	abnormal muscle spindle morphology	J:199150
	decreased muscle spindle number	J:199150
Bace1tm1Psa/Bace1tm1Psa Tg(Thy1-Nrg1*I)1Kan/0 involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6	decreased muscle spindle number	J:199150
	normal nervous system phenotype	J:199150