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Mammalian Phenotype Ontology Annotations
Query Results - Summary
N-sulfoglucosamine sulfohydrolase (sulfamidase)
28 phenotypes from 2 alleles in 2 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
abnormal bone structure J:211773
hypoactivity J:211773
increased blood urea nitrogen level J:211773
increased bone mineral content J:211773
increased bone mineral density J:211773
increased circulating alkaline phosphatase level J:211773
increased circulating potassium level J:211773
increased lean body mass J:211773
short tibia J:211773
involves: 129X1/SvJ * CD-1 * C57BL/6 * SJL
abnormal cell morphology J:72142
abnormal hair texture J:72142
abnormal heart morphology J:72142
abnormal heart valve morphology J:72142
abnormal kidney morphology J:72142
abnormal lysosome morphology J:72142
abnormal myocardium layer morphology J:72142
abnormal renal tubule morphology J:72142
abnormal vertebrae morphology J:72142
circling J:72142
corneal opacity J:72142
disheveled coat J:72142
distended urinary bladder J:72142
enlarged liver J:72142
enlarged spleen J:72142
hydronephrosis J:72142
normal nervous system phenotype J:72142
premature death J:72142
thick neurocranium J:72142

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)
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last database update
MGI 6.15
The Jackson Laboratory