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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Ostf1
osteoclast stimulating factor 1
MGI:700012
9 phenotypes from 2 alleles in 2 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Ostf1tm1(NCOM)Cmhd/Ostf1tm1(NCOM)Cmhd
C57BL/6-Ostf1tm1(NCOM)Cmhd
abnormal trabecular bone morphology J:249839
normal behavior/neurological phenotype J:249839
increased bone mineral density of femur J:249839
increased volumetric bone mineral density J:249839
normal skeleton phenotype J:249839
Ostf1tm1b(EUCOMM)Hmgu/Ostf1tm1b(EUCOMM)Hmgu
C57BL/6N-Ostf1tm1b(EUCOMM)Hmgu/Ieg
abnormal retina morphology J:211773
abnormal retina vasculature morphology J:211773
increased startle reflex J:211773
persistence of hyaloid vascular system J:211773

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
11/12/2024
MGI 6.24
The Jackson Laboratory