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Symbol
Name
ID

Slc19a2
solute carrier family 19 (thiamine transporter), member 2
MGI:1928761

Phenotype annotations related to hematopoietic system

Darker colors indicate more annotations

Human Phenotypes	Pancytopenia	Increased mean corpuscular volume	Megaloblastic anemia	Thiamine-responsive megaloblastic anemia	Sideroblastic anemia	Thrombocytopenia
Disease(s) Associated with SLC19A2	Pancytopenia	Increased mean corpuscular volume	Megaloblastic anemia	Thiamine-responsive megaloblastic anemia	Sideroblastic anemia	Thrombocytopenia
megaloblastic anemia
thiamine-responsive megaloblastic anemia syndrome

Mouse Phenotypes		abnormal definitive hematopoiesis	abnormal erythropoiesis	abnormal myelopoiesis	decreased erythrocyte cell number	thrombocytosis
Availability	Mouse Genotype	abnormal definitive hematopoiesis	abnormal erythropoiesis	abnormal myelopoiesis	decreased erythrocyte cell number	thrombocytosis
	Slc19a2^tm1Ejn/Slc19a2^tm1Ejn
	Slc19a2^tm1Gelb/Slc19a2^tm1Gelb

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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