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Symbol
Name
ID
Mgat2
mannoside acetylglucosaminyltransferase 2
MGI:2384966
Phenotype annotations related to craniofacial
Darker colors indicate more annotations
Human Phenotypes
Amelogenesis imperfecta
Abnormal facial shape
Coarse facial features
Midfrontal capillary hemangioma
Malar flattening
Midface retrusion
Everted lower lip vermilion
Smooth philtrum
Thick vermilion border
Thin vermilion border
Gingival overgrowth
High palate
Open mouth
Wide mouth
Abnormality of the dentition
Macrodontia
Diastema
Protruding tongue
Wide nose
Low hanging columella
Prominent nasal bridge
Wide nasal bridge
Thick eyebrow
Long eyelashes
Blepharophimosis
Short palpebral fissure
Downslanted palpebral fissures
Retrognathia
Microcephaly
Postnatal microcephaly
Progressive microcephaly
Macrocephaly
Prominent occiput
Brachycephaly
Dandy-Walker malformation
Disease(s) Associated with MGAT2
congenital disorder of glycosylation type II

Mouse Phenotypes
abnormal facial morphology
Availability Mouse Genotype
Mgat2tm1.1Jxm/Mgat2tm1.1Jxm

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
09/11/2018
MGI 6.12
The Jackson Laboratory