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Symbol
Name
ID

Slc46a1
solute carrier family 46, member 1
MGI:1098733

Phenotype annotations related to homeostasis/metabolism

Darker colors indicate more annotations

Human Phenotypes	Decreased circulating antibody level	Reduced blood folate concentration	Impaired folate absorption	Cerebral calcification	Basal ganglia calcification
Disease(s) Associated with SLC46A1
hereditary folate malabsorption

Mouse Phenotypes		abnormal amino acid level	increased circulating homocysteine level	increased circulating bilirubin level	decreased circulating glucose level	decreased circulating iron level	increased circulating potassium level	increased circulating aspartate transaminase level
Availability	Mouse Genotype	abnormal amino acid level	increased circulating homocysteine level	increased circulating bilirubin level	decreased circulating glucose level	decreased circulating iron level	increased circulating potassium level	increased circulating aspartate transaminase level
	Slc46a1^tm1Hija/Slc46a1^tm1Hija
	Slc46a1^{tm1b(KOMP)Mbp}/Slc46a1⁺

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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