Slc19a2 Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

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

26 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Slc19a2^tm1Ejn/Slc19a2^tm1Ejn involves: 129S4/SvJae * 129S6/SvEvTac	abnormal distortion product otoacoustic emission	J:118928
	abnormal erythropoiesis	J:101675
	arrest of male meiosis	J:101675
	azoospermia	J:101675
	cochlear inner hair cell degeneration	J:118928
	cochlear outer hair cell degeneration	J:118928
	decreased erythrocyte cell number	J:101675
	increased or absent threshold for auditory brainstem response	J:118928
	increased susceptibility to induced morbidity/mortality	J:101675
	male infertility	J:101675
	sensorineural hearing loss	J:118928
	small testis	J:101675
	thrombocytosis	J:101675
Slc19a2^tm1Gelb/Slc19a2^tm1Gelb involves: 129X1/SvJ	abnormal definitive hematopoiesis	J:79974
	abnormal erythropoiesis	J:79974
	abnormal myelopoiesis	J:79974
	abnormal reproductive system morphology	J:87410
	abnormal spermatid morphology	J:87410
	abnormal spermatogenesis	J:87410
	arrest of male meiosis	J:87410
	ataxia	J:79974
	azoospermia	J:87410
	decreased circulating insulin level	J:79974
	decreased testis weight	J:87410
	normal digestive/alimentary phenotype	J:170952
	impaired glucose tolerance	J:79974
	impaired hearing	J:79974
	increased insulin sensitivity	J:79974
	male infertility	J:87410
	premature death	J:79974

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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