29 phenotypes from 4 alleles in 4 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Ndrg1em1Lxli/Ndrg1em1Lxli C57BL/6N-Ndrg1em1Lxli	abnormal action potential	J:330126
	abnormal axon morphology	J:330126
	abnormal gait	J:330126
	abnormal motor capabilities/coordination/movement	J:330126
	abnormal sciatic nerve morphology	J:330126
	decreased body weight	J:330126
	decreased myelin sheath thickness	J:330126
	decreased nerve conduction velocity	J:330126
	demyelination	J:330126
	hindlimb paresis	J:330126
	impaired coordination	J:330126
	normal neoplasm	J:330126
	short stride length	J:330126
Ndrg1str/Ndrg1str involves: BALB/c * C57BL/6 * NOD/ShiLtWtsi	cataract	J:172770
	decreased body size	J:172770
	decreased nerve conduction velocity	J:172770
	demyelination	J:172770
	hindlimb paralysis	J:172770
	limb grasping	J:172770
	premature death	J:172770
	skeletal muscle atrophy	J:172770
	tremors	J:172770
	weakness	J:172770
Ndrg1tm1Myta/Ndrg1tm1Myta involves: 129S1/Sv * 129X1/SvJ * C57BL/6	cataract	J:172770
	decreased body size	J:172770
	decreased nerve conduction velocity	J:172770
	demyelination	J:89888, J:172770
	hindlimb paralysis	J:172770
	limb grasping	J:89888
	paraparesis	J:89888
	peripheral nervous system degeneration	J:89888
	premature death	J:172770
	skeletal muscle atrophy	J:172770
	weakness	J:172770
Ndrg1tm2b(KOMP)Wtsi/Ndrg1tm2b(KOMP)Wtsi C57BL/6N-Ndrg1tm2b(KOMP)Wtsi/Tcp	abnormal gait	J:211773
	decreased bone mineral density	J:211773
	decreased fasting circulating glucose level	J:211773
	decreased grip strength	J:211773
	decreased prepulse inhibition	J:211773
	increased circulating phosphate level	J:211773
	prolonged RR interval	J:211773
	tremors	J:211773