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Symbol
Name
ID

Pomgnt2
protein O-linked mannose beta 1,4-N-acetylglucosaminyltransferase 2
MGI:2143424

Phenotype annotations related to nervous system

Darker colors indicate more annotations

Human Phenotypes	Hydrocephalus	Ventriculomegaly	Type II lissencephaly	Cerebellar hypoplasia	Delayed speech and language development	Intellectual disability	Global developmental delay	Motor delay
Disease(s) Associated with POMGNT2	Hydrocephalus	Ventriculomegaly	Type II lissencephaly	Cerebellar hypoplasia	Delayed speech and language development	Intellectual disability	Global developmental delay	Motor delay
congenital muscular dystrophy-dystroglycanopathy type A8
muscular dystrophy-dystroglycanopathy type C8

Mouse Phenotypes		radial glial endfoot detachment	abnormal neuronal migration	abnormal cerebral cortex morphology
Availability	Mouse Genotype
	Pomgnt2^tm1Kkat/Pomgnt2^tm1Kkat

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)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 04/30/2024 MGI 6.23