34 phenotypes from 3 alleles in 5 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Eef1a2em1Abb/Eef1a2em1Abb C57BL/6JCrl-Eef1a2em1Abb	abnormal spinal cord morphology	J:296080
	decreased body weight	J:296080
	gliosis	J:296080
	neurodegeneration	J:296080
	premature death	J:296080
	sporadic seizures	J:296080
Eef1a2em#Abb/Eef1a2+ C57BL/6JCrl-Eef1a2em#Abb	abnormal behavior	J:296080
	decreased body weight	J:296080
	decreased grip strength	J:296080
	decreased skeletal muscle mass	J:296080
	impaired coordination	J:296080
Eef1a2em#Abb/Eef1a2em#Abb C57BL/6JCrl-Eef1a2em#Abb	abnormal behavior	J:296080
	abnormal spinal cord morphology	J:296080
	decreased body weight	J:296080
	gliosis	J:296080
	neurodegeneration	J:296080
	premature death	J:296080
Eef1a2wst/Eef1a2wst B6C3Fe a/a-Eef1a2wst/J	chromosomal instability	J:6766
	decreased plasma cell number	J:7903
	decreased spleen weight	J:6766
	decreased susceptibility to type IV hypersensitivity reaction	J:6766
	decreased thymus weight	J:6766
	demyelination	J:6766
	increased cellular sensitivity to gamma-irradiation	J:6766
	lymphoid hypoplasia	J:6766
	paraparesis	J:24753
	premature death	J:24753
	Purkinje cell degeneration	J:6766
	slow postnatal weight gain	J:6766
	small lymph nodes	J:6766
	tremors	J:24753
	weight loss	J:24753
Eef1a2wst/Eef1a2wst involves: HRS/J	abnormal endplate potential	J:104855
	abnormal innervation pattern to muscle	J:104855
	abnormal motor neuron morphology	J:104855
	abnormal muscle morphology	J:104855
	abnormal neuromuscular synapse morphology	J:104855
	abnormal neurotransmitter uptake	J:104855
	abnormal spinal cord ventral horn morphology	J:104855
	decreased neurotransmitter release	J:104855
	gliosis	J:104855
	impaired coordination	J:104855
	motor neuron degeneration	J:104855
Eef1a2wst/Eef1a2wst Not Specified	thymus atrophy	J:50410