31 phenotypes from 4 alleles in 6 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Psmf1em1Hs/Psmf1em1Hs Not Specified	decreased fetal size	J:282431
	fetal growth retardation	J:282431
	perinatal lethality, complete penetrance	J:282431
Psmf1tm1a(EUCOMM)Hmgu/Psmf1tm1a(EUCOMM)Hmgu involves: C57BL/6N	decreased fetal size	J:282431
	hemorrhage	J:282431
	lethality throughout fetal growth and development	J:282431
Psmf1tm1b(EUCOMM)Hmgu/Psmf1tm1b(EUCOMM)Hmgu C57BL/6N-Psmf1tm1b(EUCOMM)Hmgu/Rbrc	preweaning lethality, complete penetrance	J:211773
Psmf1tm1c(EUCOMM)Hmgu/Psmf1tm1c(EUCOMM)Hmgu Mnx1tm4(cre)Tmj/Mnx1+ involves: 129S1/Sv * C57BL/6J * C57BL/6N	abnormal axon morphology	J:282431
	abnormal motor capabilities/coordination/movement	J:282431
	abnormal neuromuscular synapse morphology	J:282431
	axon degeneration	J:282431
	decreased body weight	J:282431
	kyphosis	J:282431
	muscular atrophy	J:282431
Psmf1tm1c(EUCOMM)Hmgu/Psmf1tm1c(EUCOMM)Hmgu Tg(CDX2-cre)101Erf/0 involves: C57BL/6J * C57BL/6N * SJL/J	abnormal motor capabilities/coordination/movement	J:282431
	abnormal muscle tone	J:282431
	hindlimb paralysis	J:282431
	impaired righting response	J:282431
	limb grasping	J:282431
	postnatal lethality, complete penetrance	J:282431
	spasticity	J:282431
	tremors	J:282431
Psmf1tm1c(EUCOMM)Hmgu/Psmf1tm1c(EUCOMM)Hmgu Tg(Pcp2-cre)GN135Gsat/0 involves: C57BL/6J * C57BL/6N * FVB/N	abnormal axon morphology	J:282431
	abnormal cerebellum deep nucleus morphology	J:282431
	abnormal gait	J:282431
	abnormal locomotor behavior	J:282431
	abnormal Purkinje cell axon morphology	J:282431
	abnormal Purkinje cell dendrite morphology	J:282431
	abnormal Purkinje cell focal axonal swelling	J:282431
	abnormal synaptic bouton morphology	J:282431
	astrocytosis	J:282431
	impaired balance	J:282431
	microgliosis	J:282431
	Purkinje cell degeneration	J:282431