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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Ogn
osteoglycin
MGI:109278
5 phenotypes from 3 alleles in 3 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Ogntm1b(KOMP)Wtsi/Ogntm1b(KOMP)Wtsi
C57BL/6N-Ogntm1b(KOMP)Wtsi/J
decreased leukocyte cell number J:211773
Ogntm1Eta/Ogntm1Eta
involves: 129/Sv * C57BL/6
abnormal cornea morphology J:84062
abnormal cutaneous collagen fibril morphology J:84062
abnormal skin tensile strength J:84062
Ogntm1Hds/Ogntm1Hds
B6.129S1-Ogntm1Hds
abnormal adrenocorticotropin level J:183738

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
11/05/2019
MGI 6.14
The Jackson Laboratory