Symbol Name ID |
Slc23a1
solute carrier family 23 (nucleobase transporters), member 1 MGI:1341903 |
Allelic Composition Genetic Background |
Annotated Term | Reference |
Slc23a1tm1Mlev/Slc23a1+ involves: 129S6/SvEvTac * C57BL/6J |
abnormal blood homeostasis | J:159697 |
abnormal urine homeostasis | J:159697 | |
abnormal vitamin absorption | J:159697 | |
abnormal vitamin homeostasis | J:159697 | |
lethargy | J:159697 | |
postnatal lethality | J:159697 | |
Slc23a1tm1Mlev/Slc23a1tm1Mlev involves: 129S6/SvEvTac * C57BL/6J |
abnormal renal filtration rate | J:159697 |
abnormal urine homeostasis | J:159697 | |
abnormal vitamin absorption | J:159697 | |
abnormal vitamin C level | J:159697 | |
absent gastric milk in neonates | J:159697 | |
aminoaciduria | J:159697 | |
lethargy | J:159697 | |
maternal effect | J:159697 | |
perinatal lethality, incomplete penetrance | J:159697 | |
postnatal lethality, complete penetrance | J:159697 |
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 12/17/2024 MGI 6.24 |
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