Slc7a9 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Slc7a9
solute carrier family 7 (cationic amino acid transporter, y+ system), member 9
MGI:1353656

16 phenotypes from 1 allele in 1 genetic background

Allelic Composition Genetic Background	Annotated Term	Reference
Slc7a9^tm1Nune/Slc7a9⁺ involves: 129P2/OlaHsd * C57BL/6J	aminoaciduria	J:85462
	argininuria	J:85462
	cystinuria	J:85462
	lysinuria	J:85462
	ornithinuria	J:85462
Slc7a9^tm1Nune/Slc7a9^tm1Nune involves: 129P2/OlaHsd * C57BL/6J	abnormal circulating amino acid level	J:85462
	abnormal renal tubule morphology	J:85462
	aminoaciduria	J:85462
	argininuria	J:85462
	crystalluria	J:85462
	cystinuria	J:85462
	dilated renal tubule	J:85462
	hydronephrosis	J:85462
	hyperglutaminuria	J:85462
	increased urinary bladder weight	J:85462
	lysinuria	J:85462
	ornithinuria	J:85462
	renal cast	J:85462
	renal tubular necrosis	J:85462
	tubulointerstitial nephritis	J:85462
	urolithiasis	J:85462

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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