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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Pomgnt1
protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase
MGI:1915523
52 phenotypes from 4 alleles in 4 genetic backgrounds
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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
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
11/05/2024
MGI 6.24 		The Jackson Laboratory