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Mammalian Phenotype Ontology Annotations
Query Results - Summary
colony stimulating factor 1 receptor
78 phenotypes from 3 alleles in 5 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
involves: 129/Sv * C57BL/6J * FVB/N * SJL
abnormal skeleton morphology J:110981
absent teeth J:110981
decreased body size J:110981
increased bone mineral density J:110981
osteoporosis J:110981
premature death J:110981
round snout J:110981
abnormal brain white matter morphology J:219294
abnormal corpus callosum morphology J:219294
abnormal lateral ventricle morphology J:219294
abnormal learning/memory/conditioning J:219294
ataxia J:219294
axonal spheroids J:219294
decreased coping response J:219294
demyelination J:219294
enlarged lateral ventricles J:219294
hypermyelination J:219294
impaired coordination J:219294
impaired olfaction J:219294
increased anxiety-related response J:219294
increased oligodendrocyte progenitor number J:219294
microgliosis J:219294
neurodegeneration J:219294
neuron degeneration J:219294
abnormal bone ossification J:111489
abnormal compact bone lamellar structure J:111489
abnormal compact bone morphology J:111489
abnormal Langerhans cell physiology J:112594
abnormal limb morphology J:111489
abnormal long bone epiphyseal plate morphology J:111489
abnormal long bone epiphyseal plate proliferative zone J:111489
abnormal macrophage differentiation J:112594
abnormal osteoblast morphology J:111489
abnormal osteoclast morphology J:111489
abnormal osteocyte dendritic process morphology J:111489
abnormal osteocyte morphology J:111489
abnormal skeleton morphology J:111489
abnormal skeleton physiology J:111489
absent Langerhans cell J:112594
decreased bone mineralization J:111489
decreased bone strength J:111489
decreased compact bone thickness J:111489
delayed endochondral bone ossification J:111489
fragile skeleton J:111489
increased width of hypertrophic chondrocyte zone J:111489
postnatal lethality, complete penetrance J:111489
involves: 129X1/SvJ * C3Heb/FeJ * C57BL/6J
abnormal blood cell morphology/development J:73663
abnormal bone marrow morphology J:73663
abnormal bone structure J:73663
abnormal circulating cytokine level J:73663
abnormal leukocyte cell number J:73663
abnormal mammary gland growth during pregnancy J:73663
abnormal osteoclast differentiation J:73663
abnormal sexual interaction J:73663
abnormal skeleton morphology J:73663
abnormal spleen morphology J:73663
abnormal testes secretion J:73663
abnormal trabecular bone morphology J:73663
deafness J:73663
decreased body weight J:73663
decreased Langerhans cell number J:73663
decreased length of long bones J:73663
decreased lymphocyte cell number J:73663
decreased macrophage cell number J:73663
decreased monocyte cell number J:73663
domed cranium J:73663
failure of bone resorption J:73663
failure of tooth eruption J:73663
increased bone mineral density J:73663
increased granulocyte number J:73663
increased spleen weight J:73663
kinked tail J:73663
oligozoospermia J:73663
osteopetrosis J:73663
postnatal growth retardation J:73663
postnatal lethality J:73663
prolonged diestrus J:73663
prolonged estrous cycle J:73663
reduced male fertility J:73663
short limbs J:73663
involves: 129/Sv * C57BL/6J * SJL
no abnormal phenotype detected J:110981

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 6.14
The Jackson Laboratory