24 phenotypes from 5 alleles in 7 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Magmpc225H/Magmpc225H involves: BALB/c * C3H/HeH * C57BL/6J	abnormal gait	J:234901
Magtm1.1(KOMP)Vlcg/Magtm1.1(KOMP)Vlcg C57BL/6N-Magtm1.1(KOMP)Vlcg/J	abnormal auditory brainstem response	J:211773
	abnormal sleep behavior	J:211773
	convulsive seizures	J:211773
	decreased coping response	J:211773
	decreased leukocyte cell number	J:211773
	decreased locomotor activity	J:211773
	decreased startle reflex	J:211773
Magtm1Mtg/Magtm1Mtg B6N.129S2-Magtm1Mtg	dysmyelination	J:236408
	tomacula	J:236408
Magtm1Mtg/Magtm1Mtg either: (involves: 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	abnormal axon morphology	J:19475
	abnormal myelin sheath morphology	J:19475
	abnormal myelination	J:19475
	normal nervous system phenotype	J:19475
Magtm1Mtg/Magtm1Mtg involves: 129S2/SvPas	abnormal axon morphology	J:38760, J:78646, J:106609, J:296495
	abnormal oligodendrocyte morphology	J:38760
	abnormal Schwann cell morphology	J:106609
	axon degeneration	J:78646, J:106609
	demyelination	J:106609
Magtm1Pop/Magtm1Pop involves: 129P2/OlaHsd * C57BL/6	abnormal myelination	J:46770
Magtm1Rod/Magtm1Rod involves: 129S1/Sv * 129X1/SvJ	abnormal axon morphology	J:18407
	abnormal grooming behavior	J:18407
	decreased aggression towards mice	J:217719
	decreased locomotor activity	J:18407
	decreased prepulse inhibition	J:217719
	decreased startle reflex	J:217719
	impaired coordination	J:18407
	increased B cell proliferation	J:217719
	tremors	J:18407