Slc19a3 Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Slc19a3
solute carrier family 19, member 3
MGI:1931307

16 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Slc19a3^tm1.1Nwak/Slc19a3^tm1.1Nwak involves: C57BL/6J	abnormal locomotor behavior	J:246593
	abnormal thiamin level	J:246593
	astrocytosis	J:246593
	decreased neuron number	J:246593
	paralysis	J:246593
	premature death	J:246593
Slc19a3^tm1Said/Slc19a3^tm1Said involves: C57BL/6	abnormal liver parenchyma morphology	J:170952
	abnormal proximal convoluted tubule morphology	J:170952
	abnormal thiamin level	J:170952
	abnormal vitamin absorption	J:170952
	cachexia	J:170952
	chronic liver inflammation	J:170952
	hepatic necrosis	J:170952
	kidney inflammation	J:170952
	lethargy	J:170952
	nephrosclerosis	J:170952
	premature death	J:170952
Slc19a3^tm1Said/Slc19a3^tm1Said involves: C57BL/6J	abnormal locomotor behavior	J:246593
	abnormal thiamin level	J:246593
	astrocytosis	J:246593
	decreased neuron number	J:246593
	neurodegeneration	J:246593
	paralysis	J:246593
	premature death	J:246593

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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