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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Pomgnt2
protein O-linked mannose beta 1,4-N-acetylglucosaminyltransferase 2
MGI:2143424
9 phenotypes from 1 allele in 1 genetic background
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Allelic Composition
Genetic Background
Annotated Term Reference
Pomgnt2tm1Kkat/Pomgnt2tm1Kkat
either: B6J.Cg-Pomgnt2tm1Kkat or (involves: C57BL/6J * C57BL/6NJcl) or (involves: C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj)
abnormal basal lamina morphology J:215959
abnormal cerebral cortex morphology J:215959
abnormal enzyme/coenzyme activity J:215959
abnormal neuronal migration J:215959
decreased birth body size J:215959
decreased birth weight J:215959
decreased fetal size J:215959
neonatal lethality, complete penetrance J:215959
radial glial endfoot detachment J:215959

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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last database update
04/30/2024
MGI 6.23
The Jackson Laboratory