About   Help   FAQ
Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Slc20a1
solute carrier family 20, member 1
MGI:108392
43 phenotypes from 5 alleles in 6 genetic backgrounds
Export: Excel File
Allelic Composition
Genetic Background		 Annotated Term Reference
Slc20a1tm1.1Cmg/Slc20a1tm1.1Cmg
involves: 129S6/SvEvTac * C57BL/6 * SJL 		no abnormal phenotype detected J:156027
Slc20a1tm1.1Lbek/Slc20a1tm1.1Lbek
involves: 129S2/SvPas * C57BL/6 * C57BL/6J * SJL 		no abnormal phenotype detected J:157997
Slc20a1tm1.1Lbek/Slc20a1tm1.1Lbek
Tg(Mx1-cre)1Cgn/0
involves: 129S2/SvPas * C57BL/6 * C57BL/6J * CBA 		abnormal definitive hematopoiesis J:194198
decreased erythrocyte cell number J:194198
enlarged spleen J:194198
increased leukocyte cell number J:194198
intermingled spleen red and white pulp J:194198
spleen hyperplasia J:194198
Slc20a1tm1.2Cmg/Slc20a1tm1.2Cmg
involves: 129S6/SvEvTac * C57BL/6 * CBA * DBA/2 * SJL 		abnormal vitelline vasculature morphology J:156027
anemia J:156027
embryonic growth retardation J:156027
embryonic lethality during organogenesis, complete penetrance J:156027
Slc20a1tm1.2Lbek/Slc20a1tm1.2Lbek
involves: 129S2/SvPas * BALB/c * C57BL/6 * C57BL/6J 		abnormal erythropoiesis J:157997
abnormal liver development J:157997
anemia J:157997
decreased cell proliferation J:157997
decreased common myeloid progenitor cell number J:157997
decreased erythroid progenitor cell number J:157997
decreased hepatocyte proliferation J:157997
dilated liver sinusoidal space J:157997
embryonic growth retardation J:157997
embryonic lethality during organogenesis, complete penetrance J:157997
increased hepatocyte apoptosis J:157997
liver hypoplasia J:157997
pale liver J:157997
pale placenta J:157997
small liver J:157997
Slc20a1tm1Lbek/Slc20a1tm1.2Lbek
involves: 129S2/SvPas * BALB/c * C57BL/6 * C57BL/6J 		anemia J:157997
increased nucleated erythrocyte cell number J:157997
lethality throughout fetal growth and development, complete penetrance J:157997
liver hypoplasia J:157997
Slc20a1tm1Lbek/Slc20a1tm1.2Lbek
involves: 129S2/SvPas * C57BL/6J 		abnormal erythropoiesis J:194198
Slc20a1tm1Lbek/Slc20a1tm1Lbek
involves: 129S2/SvPas * C57BL/6J 		abnormal bone mineralization J:157997
abnormal definitive hematopoiesis J:194198
abnormal erythrocyte morphology J:157997
abnormal erythropoiesis J:194198
abnormal fatty acids level J:157997
abnormal spleen morphology J:194198
anemia J:157997, J:194198
decreased erythrocyte cell number J:157997, J:194198
decreased hematocrit J:157997
decreased hemoglobin content J:157997, J:194198
decreased mean corpuscular hemoglobin J:157997
echinocytosis J:157997
enlarged spleen J:194198
normal hematopoietic system phenotype J:194198
hemolytic anemia J:157997
increased spleen weight J:157997
pallor J:157997
postnatal growth retardation J:157997
postnatal lethality, incomplete penetrance J:157997
prenatal lethality, incomplete penetrance J:157997
reticulocytosis J:157997
schistocytosis J:157997
spherocytosis J:157997
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
06/12/2024
MGI 6.13 		The Jackson Laboratory