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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
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Allelic Composition
Genetic Background
Annotated Term Reference
Slc7a9tm1Nune/Slc7a9+
involves: 129P2/OlaHsd * C57BL/6J
aminoaciduria J:85462
argininuria J:85462
cystinuria J:85462
lysinuria J:85462
ornithinuria J:85462
Slc7a9tm1Nune/Slc7a9tm1Nune
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 tubules 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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last database update
09/10/2019
MGI 6.14
The Jackson Laboratory