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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Hfe
homeostatic iron regulator
MGI:109191
40 phenotypes from 11 alleles in 9 genetic backgrounds
Export: Excel File
Allelic Composition
Genetic Background
Annotated Term Reference
Hfetm1.1Gfn/Hfetm1.1Gfn
B6.129P2-Hfetm1.1Gfn
abnormal gait J:114351
abnormal pilomotor reflex J:114351
abnormal postural reflex J:114351
decreased body length J:114351
impaired coordination J:114351
induced hyperactivity J:114351
short tail J:114351
Hfetm1.1Jrco/Hfe+
involves: 129X1/SvJ * C57BL/6J
oxidative stress J:201948
Hfetm1.1Jrco/Hfetm1.1Jrco
involves: 129X1/SvJ * C57BL/6J
abnormal brain iron level J:201948
astrocytosis J:201948
increased body weight J:201948
increased liver iron level J:201948
oxidative stress J:201948
Hfetm1.1Nca/Hfetm1.1Nca
involves: 129S6/SvEvTac
abnormal iron level J:78536
Hfetm1.1Nca/Hfetm1.1Nca
involves: 129S6/SvEvTac * C57BL/6J
abnormal iron level J:78536
Hfetm1.1Nca/Hfetm1.1Nca
Not Specified
increased liver iron level J:62112
Hfetm1.1Wsr/Hfetm1.1Wsr
involves: 129P2/OlaHsd * C57BL/6
abnormal iron homeostasis J:141745
decreased spleen iron level J:132134
hemochromatosis J:132134
increased circulating iron level J:132134, J:132141
increased liver iron level J:132134, J:132141, J:141745
Hfetm1Gfn/Hfetm1Gfn
involves: 129P2/OlaHsd * C57BL/6
abnormal iron homeostasis J:68025
abnormal iron level J:262906
abnormal trabecular bone morphology J:262906
decreased bone trabecula number J:262906
decreased trabecular bone thickness J:262906
decreased trabecular bone volume J:262906
increased body weight J:262906
increased circulating iron level J:68025
increased liver iron level J:68025, J:262906
increased osteoclast cell number J:262906
increased spleen iron level J:68025
osteoporosis J:262906
Hfetm1Sly/Hfetm1Sly
Not Specified
increased liver iron level J:88143
Hfetm1Sly/Hfetm2Sly
involves: 129X1/SvJ * C57BL/6J
increased liver iron level J:88143
Hfetm1Wsr/Hfetm1Wsr
Lyz2tm1(cre)Ifo/?
involves: 129P2/OlaHsd * C57BL/6
normal homeostasis/metabolism phenotype J:132134
Hfetm1Wsr/Hfetm1Wsr
Tg(Alb1-cre)7Gsc/?
involves: 129P2/OlaHsd * C57BL/6 * FVB/N
decreased spleen iron level J:132134
hemochromatosis J:132134
increased circulating iron level J:132134
increased liver iron level J:132134
Hfetm1Wsr/Hfetm1Wsr
Tg(Vil1-cre)997Gum/?
involves: 129P2/OlaHsd * C57BL/6 * SJL
no abnormal phenotype detected J:141745
Hfetm2Nca/Hfe+
involves: 129S6/SvEvTac
increased liver iron level J:62112
Hfetm2Nca/Hfetm2Nca
involves: 129S6/SvEvTac
abnormal iron level J:78536
decreased spleen iron level J:78536
increased circulating iron level J:133221
increased liver iron level J:62112, J:133221
Hfetm2Nca/Hfetm2Nca
involves: 129S6/SvEvTac * C57BL/6J
abnormal iron level J:78536
decreased spleen iron level J:78536
Hfetm2Nca/Hfetm2Nca
Tg(Ttr-Hfe)1Nca/0
involves: 129S6/SvEvTac * C57BL/6
decreased circulating iron level J:133221
decreased liver iron level J:133221
hypochromic microcytic anemia J:133221
Hfetm2Sly/Hfetm2Sly
involves: 129X1/SvJ * C57BL/6J
abnormal brain iron level J:213886
abnormal brain size J:213886
abnormal object recognition memory J:213886
abnormal response to novel object J:213886
abnormal spatial reference memory J:213886
abnormal spatial working memory J:213886
decreased brain cholesterol level J:213886
decreased brain weight J:213886
decreased corpus callosum size J:213886
enlarged brain ventricles J:213886
impaired spatial learning J:213886
increased liver iron level J:88143
neuron degeneration J:213886
Hfetm2Sly/Hfetm3Sly
involves: 129X1/SvJ * C57BL/6J
increased liver iron level J:88143
Hfetm3Sly/Hfetm3Sly
involves: 129X1/SvJ * C57BL/6J
increased liver iron level J:88143

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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
04/16/2024
MGI 6.23
The Jackson Laboratory