52 phenotypes from 4 alleles in 4 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Pomgnt1Gt(OST179231)Lex/Pomgnt1Gt(OST179231)Lex involves: 129S5/SvEvBrd * C57BL/6J	abnormal basement membrane morphology	J:196379
	abnormal cerebellar foliation	J:107697
	abnormal cerebellum morphology	J:107697
	abnormal cerebral cortex morphology	J:107697
	abnormal dentate gyrus morphology	J:107697
	abnormal eye electrophysiology	J:107697
	abnormal hippocampus morphology	J:107697
	abnormal optic nerve morphology	J:107697
	abnormal retina inner limiting membrane morphology	J:196379
	abnormal retina layer morphology	J:107697
	abnormal skeletal muscle fiber morphology	J:107697
	abnormal stratification in cerebral cortex	J:107697
	abnormal tongue muscle morphology	J:107697
	normal cardiovascular system phenotype	J:107697
	centrally nucleated skeletal muscle fibers	J:107697
	decreased body size	J:107697
	decreased litter size	J:107697
	decreased retina ganglion cell number	J:107697
	dilated lateral ventricle	J:107697
	dystrophic muscle	J:107697
	impaired basement membrane formation	J:196379
	increased variability of skeletal muscle fiber size	J:107697
	limb grasping	J:107697
	male infertility	J:107697
	reduced female fertility	J:107697
	small cerebellum	J:107697
	thin cerebral cortex	J:107697
	thin retina inner nuclear layer	J:107697
	thin retina outer nuclear layer	J:107697
Pomgnt1tm1.1Cfg/Pomgnt1tm1.1Cfg involves: C57BL/6	abnormal brain pia mater morphology	J:258757
	abnormal Cajal-Retzius cell morphology	J:258757
	abnormal cerebellar hemisphere morphology	J:258757
	abnormal cerebellum external granule cell layer morphology	J:258757
	abnormal inferior colliculus morphology	J:258757
	abnormal meninges morphology	J:258757
	abnormal neocortex morphology	J:258757
	abnormal radial glial cell morphology	J:258757
	abnormal superior colliculus morphology	J:258757
	dilated lateral ventricle	J:258757
	hydrocephaly	J:258757
	preweaning lethality, complete penetrance	J:217719
Pomgnt1tm1Lex/Pomgnt1tm1Lex B6;129S5-Pomgnt1tm1Lex/Mmucd	abnormal brain development	J:171883
	abnormal retina blood vessel pattern	J:171883
	decreased circulating glucose level	J:171883
	retina degeneration	J:171883
	retina microaneurysm	J:171883
Pomgnt1tm1Stk/Pomgnt1tm1Stk involves: 129S/SvEv	abnormal enzyme/coenzyme activity	J:144746, J:144928
	abnormal muscle physiology	J:144928
	abnormal muscle regeneration	J:144928
	abnormal skeletal muscle satellite cell proliferation	J:144928
	decreased body size	J:144928
	decreased skeletal muscle fiber number	J:144928
	decreased skeletal muscle fiber size	J:144928
	dystrophic muscle	J:144928
	postnatal lethality, incomplete penetrance	J:144928