Ogn Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Ogn
osteoglycin
MGI:109278

8 phenotypes from 3 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Ogn^{tm1b(KOMP)Wtsi}/Ogn^{tm1b(KOMP)Wtsi} C57BL/6N-Ogn^{tm1b(KOMP)Wtsi}/J	decreased leukocyte cell number	J:211773
	hyperactivity	J:211773
	increased fasting circulating glucose level	J:211773
	prolonged RR interval	J:211773
Ogn^tm1Eta/Ogn^tm1Eta involves: 129/Sv * C57BL/6	abnormal cornea morphology	J:84062
	abnormal cutaneous collagen fibril morphology	J:84062
	abnormal skin tensile strength	J:84062
Ogn^tm1Hds/Ogn^tm1Hds B6.129S1-Ogn^tm1Hds	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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