Slc48a1 Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Slc48a1
solute carrier family 48 (heme transporter), member 1
MGI:1914989

25 phenotypes from 3 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Slc48a1^em1(IMPC)Bay/Slc48a1⁺ C57BL/6N-Slc48a1^em1(IMPC)Bay/BayMmucd	decreased bone mineral content	J:211773
	decreased locomotor activity	J:211773
	limb grasping	J:211773
Slc48a1^em1Ih/Slc48a1^em1Ih involves: 129 * C57BL/6J	abnormal bone marrow morphology	J:282829
	abnormal calcium level	J:282829
	abnormal copper level	J:282829
	abnormal iron level	J:282829
	abnormal liver morphology	J:282829
	abnormal macrophage morphology	J:282829
	abnormal macrophage physiology	J:282829
	abnormal spleen morphology	J:282829
	abnormal stress erythropoiesis	J:282829
	abnormal sulfate level	J:282829
	abnormal susceptibility to induced morbidity/mortality	J:282829
	anemia	J:282829
	decreased hematocrit	J:282829
	decreased macrophage cell number	J:282829
	enlarged spleen	J:282829
	extramedullary hematopoiesis	J:282829
	impaired hematopoiesis	J:282829
	increased circulating ferritin level	J:282829
	increased erythroblast number	J:282829
	increased liver iron level	J:282829
	increased spleen iron level	J:282829
Slc48a1^{Gt(U3Betageo)1Ruiz}/Slc48a1^{Gt(U3Betageo)1Ruiz} involves: 129S2/SvPas * C57BL/6	no abnormal phenotype detected	J:85162

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)
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