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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Epo
erythropoietin
MGI:95407
45 phenotypes from 6 alleles in 8 genetic backgrounds
Export: Excel File
Allelic Composition
Genetic Background
Annotated Term Reference
EpoTg(SV40T/Epo)134.3LCPjr/Epo+
(C57BL/10 x CBA)F1 X CFLP
anemia J:128415
EpoTg(SV40T/Epo)134.3LCPjr/Epo+
involves: C57BL/6 * CBA
anemia J:79374
EpoTg(SV40T/Epo)134.3LCPjr/EpoTg(SV40T/Epo)134.3LCPjr
(C57BL/10 x CBA)F1 X CFLP
anemia J:128415
EpoTg(SV40T/Epo)134.3LCPjr/EpoTg(SV40T/Epo)134.3LCPjr
involves: C57BL/6 * CBA
anemia J:79374, J:128248
decreased oxygen consumption J:128248
enlarged myocardial fiber J:79374
hemosiderosis J:79374
hyperoxia J:128248
hyperventilation J:128248
hypoxia J:79374
increased heart right ventricle weight J:128242, J:128248
increased heart weight J:79374
increased left ventricle weight J:128248
increased pulmonary ventilation J:128242, J:128248
increased spleen weight J:79374
Epotm1.1Mym/Epotm1.1Mym
Not Specified
no abnormal phenotype detected J:175070
Epotm1.2Mym/Epotm1.2Mym
Not Specified
abnormal erythropoiesis J:175070
abnormal liver morphology J:175070
abnormal liver physiology J:175070
anemia J:175070
decreased fetal derived definitive erythrocyte cell number J:175070
decreased hematocrit J:175070
normal mortality/aging J:175070
pale liver J:175070
pallor J:175070
small liver J:175070
Epotm1.2Mym/Epotm1.2Mym
Tg(Epo*)458Mym/0
involves: C57BL/6 * DBA/2
abnormal femur morphology J:231255
abnormal spleen morphology J:231255
anemia J:231255
decreased bone marrow cell number J:231255
decreased erythroblast number J:231255
decreased hematocrit J:231255
enlarged heart J:231255
Epotm1.2Mym/Epotm1.2Mym
Tg(Epo*)458Mym/Tg(Epo*)458Mym
involves: C57BL/6 * DBA/2
anemia J:231255
Epotm1Jae/Epotm1Jae
either: (involves: 129S4/SvJae * BALB/c) or (involves: 129S4/SvJae * C57BL/6)
abnormal erythropoiesis J:29254
abnormal placenta morphology J:29254
anemia J:29254
increased erythroid progenitor cell number J:29254
increased hepatocyte apoptosis J:29254
lethality throughout fetal growth and development, complete penetrance J:29254
pale liver J:29254
small liver J:29254
Epotm1Jae/Epotm1Jae
involves: 129S4/SvJae
abnormal blood vessel morphology J:53885
abnormal epicardium morphology J:53885
abnormal heart development J:53885
abnormal interventricular groove morphology J:53885
abnormal interventricular septum morphology J:53885
abnormal myocardial fiber physiology J:53885
anemia J:53885
decreased angiogenesis J:128893
edema J:53885
lethality throughout fetal growth and development, complete penetrance J:53885
pericardial edema J:53885
thick ventricular wall J:53885
ventricular hypoplasia J:53885
Epotm1Knni/Epotm1Knni
Gt(ROSA)26Sortm9(cre/ESR1)Arte/Gt(ROSA)26Sor+
involves: 129S/Sv * C57BL/6
abnormal erythropoiesis J:165479
decreased erythrocyte cell number J:165479
decreased hematocrit J:165479
decreased hemoglobin content J:165479
Epotm1Knni/Epotm1Knni
Tg(EIIa-cre)C5379Lmgd/0
involves: C57BL/6 * FVB/N
decreased erythrocyte cell number J:165479
embryonic lethality during organogenesis, complete penetrance J:165479

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last database update
05/14/2019
MGI 6.14
The Jackson Laboratory