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Symbol
Name
ID

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

Phenotype annotations related to reproductive system

Darker colors indicate more annotations

Human Phenotypes	Cryptorchidism
Disease(s) Associated with SLC19A2	Cryptorchidism
thiamine-responsive megaloblastic anemia syndrome

Mouse Phenotypes		azoospermia	abnormal spermatid morphology	decreased testis weight	small testis	abnormal reproductive system morphology	arrest of male meiosis	abnormal spermatogenesis	male infertility
Availability	Mouse Genotype	azoospermia	abnormal spermatid morphology	decreased testis weight	small testis	abnormal reproductive system morphology	arrest of male meiosis	abnormal spermatogenesis	male infertility
	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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