Slc26a1 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Slc26a1
solute carrier family 26 (sulfate transporter), member 1
MGI:2385894

13 phenotypes from 1 allele in 1 genetic background

Allelic Composition Genetic Background	Annotated Term	Reference
Slc26a1^tm1Mark/Slc26a1^tm1Mark involves: 129X1/SvJ * CD-1	abnormal digestive system physiology	J:158567
	abnormal liver physiology	J:158567
	abnormal mineral level	J:158567
	abnormal vesicle-mediated transport	J:158567
	hepatic necrosis	J:158567
	hyposulfatemia	J:158567
	increased circulating alanine transaminase level	J:158567
	increased circulating calcium level	J:158567
	increased physiological sensitivity to xenobiotic	J:158567
	increased urine calcium level	J:158567
	increased urine sulfate level	J:158567
	kidney inflammation	J:158567
	nephrolithiasis	J:158567

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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