About   Help   FAQ
Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Csf1r
colony stimulating factor 1 receptor
MGI:1339758
78 phenotypes from 3 alleles in 5 genetic backgrounds
Export: Excel File
Allelic Composition
Genetic Background		 Annotated Term Reference
Csf1rtm1.1Jwp/Csf1rtm1.1Jwp
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
Csf1rtm1Ers/Csf1r+
B6.129X1-Csf1rtm1Ers 		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
Csf1rtm1Ers/Csf1rtm1Ers
FVB.129X1-Csf1rtm1Ers 		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
Csf1rtm1Ers/Csf1rtm1Ers
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 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
decreased testes secretion 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
Csf1rtm1Jwp/Csf1rtm1Jwp
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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support. 		last database update
11/19/2024
MGI 6.24 		The Jackson Laboratory