Pomgnt2 Phenotype Annotations

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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

Allelic Composition Genetic Background	Annotated Term	Reference
Pomgnt2^tm1Kkat/Pomgnt2^tm1Kkat either: B6J.Cg-Pomgnt2^tm1Kkat 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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