53 phenotypes from 7 alleles in 7 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Pla2g6m1J/Pla2g6m1J C3H/HeJ-Pla2g6m1J	abnormal astrocyte physiology	J:183152
	decreased grip strength	J:183152
	neurodegeneration	J:183152
	premature death	J:183152
	tremors	J:183152
	weight loss	J:183152
Pla2g6m1Sein/Pla2g6m1Sein C57BL/6JJcl-Pla2g6m1Sein	abnormal astrocyte physiology	J:183152
	abnormal axon morphology	J:153195
	abnormal brain morphology	J:153195
	abnormal brain white matter morphology	J:153195
	abnormal brainstem morphology	J:153195
	abnormal motor capabilities/coordination/movement	J:155328
	abnormal motor coordination/balance	J:153195
	abnormal nervous system morphology	J:153195, J:155328
	abnormal spinal cord morphology	J:153195
	ataxia	J:155328
	axonal dystrophy	J:183152
	decreased double-positive T cell number	J:155328
	decreased grip strength	J:155328
	hindlimb paralysis	J:155328
	muscular atrophy	J:153195
	neurodegeneration	J:183152
	premature death	J:153195, J:155328
	skeletal muscle atrophy	J:155328
	weight loss	J:155328
Pla2g6tm1.1Hlw/Pla2g6tm1.1Hlw involves: 129 * C57BL/6J	abnormal mitochondrial crista morphology	J:317126
	abnormal mitochondrial morphology	J:317126
	abnormal mitochondrial physiology	J:317126
	abnormal mitophagy	J:317126
	abnormal substantia nigra pars compacta morphology	J:317126
	abnormal synaptic bouton morphology	J:317126
	bradykinesia	J:317126
	decreased locomotor activity	J:317126
	decreased mitochondrial size	J:317126
	decreased vertical activity	J:317126
	impaired coordination	J:317126
	increased endoplasmic reticulum stress	J:317126
	Lewy bodies	J:317126
	neuron degeneration	J:317126
	oxidative stress	J:317126
Pla2g6tm1a(EUCOMM)Wtsi/Pla2g6tm1a(EUCOMM)Wtsi C57BL/6N-Pla2g6tm1a(EUCOMM)Wtsi/Wtsi	male infertility	J:211773
Pla2g6tm1Tsu/Pla2g6tm1Tsu involves: 129S2/SvPas * C57BL/6	abnormal axon morphology	J:174587
	abnormal cell cytoskeleton morphology	J:174587
	abnormal gait	J:132853
	abnormal mitochondrial crista morphology	J:174587
	abnormal mitochondrial morphology	J:174587
	abnormal myelin sheath morphology	J:174587
	abnormal sciatic nerve morphology	J:132853, J:174587
	abnormal spinal cord grey matter morphology	J:174587
	abnormal spinal cord ventral horn morphology	J:174587
	abnormal synaptic bouton morphology	J:174587
	ataxia	J:132853
	axon degeneration	J:174587
	axonal dystrophy	J:174587
	axonal spheroids	J:174587
	impaired coordination	J:132853
	impaired limb coordination	J:132853
	kyphosis	J:132853
	neurodegeneration	J:132853
	premature death	J:132853
	reduced male fertility	J:132853
	weight loss	J:132853
Pla2g6tm1Turk/Pla2g6tm1Turk involves: 129X1/SvJ	abnormal gait	J:131429
	abnormal locomotor coordination	J:131429
	abnormal motor coordination/balance	J:131429
	asthenozoospermia	J:92835
	impaired coordination	J:131429
	impaired limb coordination	J:131429
	increased exploration in new environment	J:131429
	neurodegeneration	J:131429
	reduced male fertility	J:92835
Pla2g6tm1Zyao/Pla2g6tm1Zyao involves: 129S6/SvEvTac * C57BL/6	abnormal apolipoprotein level	J:203038
	blindness	J:203038
	increased cholesterol level	J:203038
	male infertility	J:203038