Slc20a1 Phenotype Annotations

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

Allelic Composition Genetic Background	Annotated Term	Reference
Slc20a1^tm1.1Cmg/Slc20a1^tm1.1Cmg involves: 129S6/SvEvTac * C57BL/6 * SJL	no abnormal phenotype detected	J:156027
Slc20a1^tm1.1Lbek/Slc20a1^tm1.1Lbek involves: 129S2/SvPas * C57BL/6 * C57BL/6J * SJL	no abnormal phenotype detected	J:157997
Slc20a1^tm1.1Lbek/Slc20a1^tm1.1Lbek 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
Slc20a1^tm1.2Cmg/Slc20a1^tm1.2Cmg 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
Slc20a1^tm1.2Lbek/Slc20a1^tm1.2Lbek 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
Slc20a1^tm1Lbek/Slc20a1^tm1.2Lbek 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
Slc20a1^tm1Lbek/Slc20a1^tm1.2Lbek involves: 129S2/SvPas * C57BL/6J	abnormal erythropoiesis	J:194198
Slc20a1^tm1Lbek/Slc20a1^tm1Lbek 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

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