Slc13a1 Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Slc13a1
solute carrier family 13 (sodium/sulfate symporters), member 1
MGI:1859937

17 phenotypes from 1 allele in 1 genetic background

Allelic Composition Genetic Background	Annotated Term	Reference
Slc13a1^tm1Mark/Slc13a1⁺ involves: 129T2/SvEms * C57BL/6J	abnormal enzyme/coenzyme activity	J:86561
	abnormal renal reabsorption	J:86561
	clonic seizures	J:86561
	hyposulfatemia	J:86561
	increased bile salt level	J:86561
	increased urine sulfate level	J:86561
Slc13a1^tm1Mark/Slc13a1^tm1Mark involves: 129T2/SvEms * C57BL/6J	abnormal enzyme/coenzyme activity	J:86561
	abnormal renal reabsorption	J:86561
	normal cardiovascular system phenotype	J:86561
	clonic seizures	J:86561
	decreased body size	J:86561
	decreased body weight	J:86561
	decreased circulating insulin-like growth factor I level	J:86561
	decreased litter size	J:86561
	hyposulfatemia	J:86561
	increased bile salt level	J:86561
	increased liver weight	J:86561
	increased miscarriage rate	J:86561
	increased urine sulfate level	J:86561
	postnatal growth retardation	J:86561
	reduced female fertility	J:86561
	short femur	J:86561
	short tail	J:86561

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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