Symbol Name ID |
Mgat2
mannoside acetylglucosaminyltransferase 2 MGI:2384966 |
Darker colors indicate more annotations |
Human Phenotypes | Abnormal scalp morphology |
Brachycephaly |
Dolichocephaly |
Mandibular prognathia |
Retrognathia |
Microcephaly |
Progressive microcephaly |
Macrocephaly |
Abnormal facial shape |
Midfrontal capillary hemangioma |
Everted lower lip vermilion |
Long philtrum |
Thin vermilion border |
Gingival overgrowth |
Protruding tongue |
Open mouth |
Wide mouth |
Macrodontia |
Dental crowding |
Diastema |
Low hanging columella |
Convex nasal ridge |
Prominent nasal bridge |
Recurrent upper and lower respiratory tract infections |
Thick eyebrow |
Long eyelashes |
Downslanted palpebral fissures |
Disease(s) Associated with MGAT2 | |||||||||||||||||||||||||||
congenital disorder of glycosylation type IIa |
Mouse Phenotypes | abnormal facial morphology |
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Availability | Mouse Genotype | |
Mgat2tm1.1Jxm/Mgat2tm1.1Jxm |
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 04/23/2024 MGI 6.23 |
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