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Mammalian Phenotype Ontology Annotations
Query Results - Summary
mannoside acetylglucosaminyltransferase 2
41 phenotypes from 1 allele in 2 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
involves: 129S1/Sv * 129X1/SvJ * C57BL/6
abnormal blood coagulation J:80661
abnormal digestion J:80661
abnormal facial morphology J:80661
abnormal locomotor behavior J:80661
abnormal muscle development J:80661
abnormal PNS synaptic transmission J:80661
anemia J:80661
decreased body size J:80661
decreased bone mineral density J:80661
decreased circulating calcium level J:80661
decreased circulating total protein level J:80661
decreased fetal size J:80661
delayed bone ossification J:80661
gastrointestinal hemorrhage J:80661
hypoglycemia J:80661
increased mean corpuscular volume J:80661
kyphoscoliosis J:80661
lethality throughout fetal growth and development, incomplete penetrance J:80661
normal nervous system phenotype J:80661
paralysis J:80661
postnatal lethality, complete penetrance J:80661
rectal prolapse J:80661
reticulocytosis J:80661
tremors J:80661
involves: 129S1/Sv * 129X1/SvJ * ICR
abnormal B cell differentiation J:80661
abnormal maternal nurturing J:80661
abnormal motor coordination/balance J:80661
abnormal testis morphology J:80661
arrest of male meiosis J:80661
azoospermia J:80661
decreased body size J:80661
decreased grip strength J:80661
decreased T cell number J:80661
enlarged lymph nodes J:80661
enlarged spleen J:80661
glomerulonephritis J:80661
hematuria J:80661
increased urine protein level J:80661
male infertility J:80661
postnatal lethality, incomplete penetrance J:80661
prenatal lethality, incomplete penetrance J:80661
reduced female fertility J:80661

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last database update
MGI 6.11
The Jackson Laboratory