Slc48a1 Phenotype Annotations - Multigenic Genotypes

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

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

5 phenotypes from multigenic genotypes

Allelic Composition Genetic Background	Annotated Term	Reference
Hmox1^tm1Poss/Hmox1⁺ Slc48a1^em1Ih/Slc48a1^em1Ih involves: 129 * 129S2/SvPas * C57BL/6J	decreased macrophage cell number	J:282829
	impaired hematopoiesis	J:282829
	increased erythroid progenitor cell number	J:282829
	prenatal lethality, incomplete penetrance	J:282829
Hmox1^tm1Poss/Hmox1^tm1Poss Slc48a1^em1Ih/Slc48a1^em1Ih involves: 129 * 129S2/SvPas * C57BL/6J	anemia	J:282829
	decreased macrophage cell number	J:282829
	prenatal lethality, incomplete penetrance	J:282829

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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