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Symbol
Name
ID
Mgat2
mannoside acetylglucosaminyltransferase 2
MGI:2384966
Phenotype annotations related to skeleton
Darker colors indicate more annotations
Human Phenotypes
Amelogenesis imperfecta
Malar flattening
Retrognathia
Microcephaly
Postnatal microcephaly
Progressive microcephaly
Macrocephaly
Prominent occiput
Brachycephaly
Dandy-Walker malformation
Short neck
Coxa valga
Proximal placement of thumb
Overlapping fingers
Postaxial polydactyly
Metaphyseal dysplasia
Rhizomelia
Diaphyseal dysplasia
Epiphyseal dysplasia
Slender long bone
Abnormality of the rib cage
Pectus excavatum
Thoracolumbar kyphoscoliosis
Thoracic scoliosis
Butterfly vertebrae
Vertebral segmentation defect
Kyphoscoliosis
Osteopenia
Osteoporosis
Joint laxity
Recurrent fractures
Disease(s) Associated with MGAT2
congenital disorder of glycosylation type II

Mouse Phenotypes
kyphoscoliosis
decreased bone mineral density
delayed bone ossification
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
06/12/2018
MGI 6.12
The Jackson Laboratory